DermatitisPhase 3NCT03627767
Study to Investigate Efficacy and Safety of PF-04965842 in Subjects Aged 12 Years and Over With Moderate to Severe Atopic Dermatitis With the Option of Rescue Treatment in Flaring Subjects
A Phase 3 study testing PF-04965842 100 mg and PF-04965842 200 mg in people with Dermatitis and Dermatitis, Atopic, run by Pfizer at 235 sites in 21 countries.
Trial summary
B7451014 is a Phase 3 study to investigate PF-04965842 in patients aged 12 years and over with a minimum body weight of 40 kg who have moderate to severe atopic dermatitis. Subjects responding well to an initial open-label 12 week treatment of PF-04965842 (200 mg) taken orally once daily (QD) will be identified and… Read more about this study
- Who is it for?
- Ages 12 years and older
- Conditions the study is for
- Dermatitis, Dermatitis, Atopic, Eczema
- What is being tested?
- PF-04965842 100 mg and PF-04965842 200 mg
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 1,235 participants
- Where
- 235 sitesin 21 countries
- Study dates
- 11 Jun 2018to 7 Oct 2020
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 12 years of age or older with a minimum body weight of 40 kg
- Diagnosis of atopic dermatitis (AD) for at least 1 year and current status of moderate to severe disease (>= the following scores: BSA10%, IGA 3, EASI 16, Pruritus NRS 4)
- Recent history of inadequate response or inability to tolerate topical AD treatments or require systemic treatments for AD control
Who cannot join
- Unwilling to discontinue current AD medications prior to the study or require treatment with prohibited medications during the study
- Prior treatment with JAK inhibitors
- Other active nonAD inflammatory skin diseases or conditions affecting skin
- Medical history including thrombocytopenia, coagulopathy or platelet dysfunction, Q wave interval abnormalities, current or history of certain infections, cancer, lymphoproliferative disorders and other medical conditions at the discretion of the investigator
- Pregnant or breastfeeding women, or women of childbearing potential who are unwilling to use contraception
Trial locations and contacts
235 sites in 21 countries.
235 sites in 21 countries
United States52 sites
Emory University
Atlanta, Georgia, 30322
Meridian Clinical Research, LLC
Baton Rouge, Louisiana, 70808
Bay Pines VAHCS
Bay Pines, Florida, 33744
Bexley Dermatology Research
Bexley, Ohio, 43209
Total Skin and Beauty Dermatology Center, PC
Birmingham, Alabama, 35205
University of Alabama at Birmingham, Dermatology at the Whitaker Clinic
Birmingham, Alabama, 35233
Clinical Research Center of Alabama, LLC
Birmingham, Alabama, 35244
Skin Care Research, LLC
Boca Raton, Florida, 33486
Tufts Medical Center
Boston, Massachusetts, 02111
Skin Research Institute
Coral Gables, Florida, 33146
Dermatology Treatment & Research Center, PA
Dallas, Texas, 75230
Innovate Research, LLC
Fort Worth, Texas, 76244
Tien Q Nguyen MD Inc dba First OC Dermatology
Fountain Valley, California, 92708
Center for Dermatology Clinical Research, Inc.
Fremont, California, 94538
The University of Texas Health Science Center Houston
Houston, Texas, 77030
Ventavia Research Group Hurst
Hurst, Texas, 76054
Dawes Fretzin Clinical Research Group, LLC
Indianapolis, Indiana, 46250
Forest Hills Dermatology Group
Kew Gardens, New York, 11374
Beach Allergy and Asthma Specialty Group, A Medical Corporation
Long Beach, California, 90808
DXP Imaging
Louisville, Kentucky, 40216
Skin Sciences PLLC
Louisville, Kentucky, 40217
Dermatologic Surgery Specialists, PC
Macon, Georgia, 31217
Baumann Cosmetic and Research Institute
Miami, Florida, 33137
Ds Research
New Albany, Indiana, 47150
Tulane University Health Sciences Center
New Orleans, Louisiana, 70112
Juva Skin and Laser Center
New York, New York, 10022
Virginia Clinical Research, Inc
Norfolk, Virginia, 23502
Midwest Allergy Sinus Asthma, SC
Normal, Illinois, 61761
Dermatology Specialists, Inc.
Oceanside, California, 92056
Lynn Health Science Institute
Oklahoma City, Oklahoma, 73112
Newton Clinical Research
Oklahoma City, Oklahoma, 73120
Park Avenue Dermatology
Orange Park, Florida, 32073
Kansas City Dermatology, P.A.
Overland Park, Kansas, 66215
Qualmedica Research, LLC
Owensboro, Kentucky, 42301
Owensboro Dermatology Associates
Owensboro, Kentucky, 42303
Paddington Testing Co, Inc.
Philadelphia, Pennsylvania, 19103
The Indiana Clinical Trials Center
Plainfield, Indiana, 46168
Oregon Medical Research Center
Portland, Oregon, 97223
M3 - Wake Research, Inc.
Raleigh, North Carolina, 27612
Health Concepts
Rapid City, South Dakota, 57702
Mayo Clinic
Rochester, Minnesota, 55905
UR Dermatology at College Town
Rochester, New York, 14620
MediSearch Clinical Trials
Saint Joseph, Missouri, 64506
University of California San Diego
San Diego, California, 92122
San Luis Dermatology and Laser Clinic
San Luis Obispo, California, 93405
Southern California Dermatology, Inc.
Santa Ana, California, 92701
Mosaic Dermatology
Santa Monica, California, 90403
Dermatology Associates of Seattle
Seattle, Washington, 98101
NorthShore University HealthSystem Dermatology Clinical Trials Unit
Skokie, Illinois, 60077
Dermatology Specialists of Spokane
Spokane, Washington, 99202
Saint Louis University Dermatology
St Louis, Missouri, 63104
USF Asthma, Allergy & Immunology Clinical Research Unit
Tampa, Florida, 33613
Poland28 sites
Nasz Lekarz Osrodek Badan Klinicznych
Bydgoszcz, 85-065
Centrum Medyczne SENSEMED
Chorzów, 41-500
Copernicus Podmiot Leczniczy Sp. z.o.o., Oddzial Dermatologii
Gdansk, 80-152
Uniwersyteckie Centrum Kliniczne, Klinika Dermatologii, Wenerologii i Alergologii
Gdansk, 80-214
Silmedic Sp. z o.o., Oddzial w Katowicach
Katowice, 40-282
Centrum Medyczne Angelius Provita
Katowice, 40-611
Pro Familia Altera Sp. z o.o.
Katowice, 40-648
Malopolskie Centrum Kliniczne
Krakow, 30-149
Centrum Badan Klinicznych JCI
Krakow, 30-348
Krakowskie Centrum Medyczne Sp. z o.o.
Krakow, 31-501
Centrum Terapii Wspolczesnej J.M. Jasnorzewska Spolka Komandytowo-Akcyjna
Lodz, 90-242
NZOZ "DERMED" Centrum Medyczne Sp. z o.o. - Oddzial w Lodzi
Lodz, 90-265
O?rodek Bada? Klinicznych Appletreeclinics
Lodz, 90-349
Dermoklinika-Centrum Medyczne s.c.
Lodz, 90-436
KO-MED Centra Kliniczne Lublin II
Lublin, 20-362
Dermedic Jacek Zdybski
Ostrowiec Świętokrzyski, 27-400
Laser Clinic S.C. dr Tomasz Kochanowski dr Andrzej Krolicki
Szczecin, 70-332
Alergo-Med Specjalistyczna Przychodnia Lekarska Sp. z o.o.
Tarnów, 33-100
Synexus Polska Sp. z o.o. Oddzial w Warszawie
Warsaw, 01-192
MTZ Clinical Research Sp. z o.o.
Warsaw, 02-106
Centralny Szpital Kliniczny Ministerstwa Spraw Wewnetrznych i Administracji w Warszawie
Warsaw, 02-507
RCMed Oddzial Warszawa
Warsaw, 02-657
Klinika Ambroziak Sp. z o.o.
Warsaw, 02-758
ETG Warszawa
Warsaw, 02-793
Wojskowy Instytut Medyczny, Klinika Dermatologiczna
Warsaw, 04-141
Synexus Polska Sp. z o.o. Oddzial we Wroclawiu
Wroclaw, 50-381
Lukasz Matusiak "4Health'
Wroclaw, 50-566
Kliniczny Oddzial Chorob Wewnetrznych, Dermatologii i Alergologii
Zabrze, 41-800
China20 sites
Beijing Friendship Hospital, Capital Medical University
Beijing, Beijing Municipality, 100050
Peking University First Hospital
Beijing, 100034
The Second Xiangya Hospital of Central South University
Changsha, Hunan, 410011
The Third Xiangya Hospital of Central South University
Changsha, Hunan, 410013
The Second Affiliated Hospital of Army Medical University, PLA
Chongqing, Chongqing Municipality, 400037
The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, 510080
The Third Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, 510630
The First Affiliated Hospital of Zhejiang University School of Medicine/Dermatology and STD Dept
Hangzhou, Zhejiang, 310003
The Second Affiliated Hospital of Zhejiang University School of Medicine/Dermatology Dept
Hangzhou, Zhejiang, 310009
Zhejiang Provincial People's Hospital/Dermatology Department
Hangzhou, Zhejiang, 310014
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, 310016
Jinan Central Hospital
Jinan, Shandong, 250013
Dermatology Hospital of Jiangxi Province
Nanchang, Jiangxi, 330000
The First Affiliated Hospital With Nanjing University
Nanjing, Jiangsu, 210000
Huashan Hospital Fudan University
Shanghai, Shanghai Municipality, 200040
Shanghai Changzheng Hospital
Shanghai, 200003
Shanghai Dermatology Hospital
Shanghai, 200443
The University of Hong Kong - Shenzhen Hospital
Shenzhen, Guangdong, 518053
Tianjin Medical University General Hospital, Dermatological Department
Tianjin, Tianjin Municipality, 300052
Tongji Hospital, Tongji Medical College,Huazhong University of Science and Technology
Wuhan, Hubei, 430030
Germany18 sites
Charite - Universitaetsmedizin Berlin, Klinik fuer Dermatologie, Venerologie und Allergologie
Berlin, 10117
Hautzentrum Friedrichshain Studien
Berlin, 10247
Rothhaar Studien GmbH
Berlin, 10783
Klinikum Bielefeld Rosenhoehe
Bielefeld, 33647
Universitaetsklinikum Bonn
Bonn, 53127
Universitaetsklinikum Carl Gustav Carus der Technischen Universitaet Dresden
Dresden, 01307
Universitaetsklinikum Erlangen
Erlangen, 91054
Universitaetsklinikum Essen
Essen, 45147
SRH Wald-Klinikum Gera GmbH
Gera, 07548
Universitätsklinikum und Poliklinik für Dermatologie und Venerologie
Halle, 06120
Klinische Forschung Hamburg GmbH
Hamburg, 20253
TFS Trial Form Support GmbH
Hamburg, 20537
Katholisches Kinderkrankenhaus Wilhemstift
Hamburg, 22149
MENSINGDERMA research GmbH
Hamburg, 22391
Medizinische Hochschule Hannover
Hanover, 30625
Praxis Dr. med. Beate Schwarz
Langenau, 89129
Universitaetsklinikum Schleswig-Holstein
Lübeck, 23538
Hautaerztliche Gemeinschaftspraxis Dres. Leitz und Kollegen
Stuttgart, 70178
Canada16 sites
CCA Medical Research
Ajax, Ontario, L1S 7K8
SimcoDerm Medical and Surgical Dermatology Center
Barrie, Ontario, L4M 7G1
Dermatology Research Institute
Calgary, Alberta, T1Y0B4
Stratica Medical
Edmonton, Alberta, T5K 1X3
Alberta Dermasurgery Center
Edmonton, Alberta, T6G1C3
Lynderm Research Inc.
Markham, Ontario, L3P 1X2
DermEdge Research
Mississauga, Ontario, L5H 1G9
Dermatology Ottawa Research Centre
Ottawa, Ontario, K2C 3N2
SKiN Centre for Dermatology
Peterborough, Ontario, K9J 5K2
Centre de Recherche Dermatologique du Quebec Metropolitain (CRDQ)
Québec, Quebec, G1V 4X7
Office of Dr. Paul Adam
Scarborough Village, Ontario, M1B 4Z8
Karma Clinical Trials, Inc.
St. John's, Newfoundland and Labrador, A1A 4Y3
AvantDerm
Toronto, Ontario, M5A 3R6
K. Papp Clinical Research
Waterloo, Ontario, N2J 1C4
XLR8 Medical Research Inc.
Windsor, Ontario, N8W 1E6
Wiseman Dermatology Research Inc.
Winnipeg, Manitoba, R3M 3Z4
Russia15 sites
SBIH "Chelyabinsk Regional Clinical Dermatovenerology dispensary"
Chelyabinsk, 454048
Limited Liability Company "Medical Center "Rheuma-Med"
Kemerovo, 650070
Clinic of FSBEI HE Kirov SMU MOH Russia
Kirov, 610014
FSBI "State Research Centre of Dermatovenereology and Cosmetology" MoH RF
Moscow, 107076
NRC Institute of Immunology FMBA of Russia
Moscow, 115478
SBI RR "Skin and Venereal Dispensary"
Rostov-on-Don, 344007
SBI RR "Regional Clinical Skin and Veneral Dispensary"
Ryazan, 390046
LLC "Pierre Wolkenstein Clinic of Skin Diseases"
Saint Petersburg, 191123
Vitiligo center
Saint Petersburg, 191123
SPb SBIH "Dermatovenerologic Dispensary #10 - Clinic of dermatology and venerology"
Saint Petersburg, 194021
FSBEI HE "St. Petersburg State Pediatric Medical University" MoH RF
Saint Petersburg, 194100
Limited Liability Company "Sanavita"
Saint Petersburg, 195257
Medical Research Institute, LLC
Saint Petersburg, 196084
FSBEI HE I.P.Pavlov SPbSMU MOH Russia
Saint Petersburg, 197022
RSBIH "Smolensk Regional Clinical Hospital"
Smolensk, 214018
Spain15 sites
Hospital General Universitario de Alicante
Alicante, 03010
Hospital Universitari Germans Trias i Pujol
Badalona, Barcelona, 08916
Hospital Clinic de Barcelona
Barcelona, 08036
Hospital de la Santa Creu i Sant Pau
Barcelona, 08041
Hospital Universitario Reina Sofia
Córdoba, 14004
Hospital Sant Joan de Deu
Esplugues de Llobregat, Barcelona, 08950
Hospital Universitario de La Princesa
Madrid, 28006
Hospital General Universitario Gregorio Maranon
Madrid, 28007
Hospital Universitario Infanta Leonor
Madrid, 28031
Hospital Universitario La Paz
Madrid, 28046
Hospital del Nino Jesus
Madrid, 28089
Hospital Universitario Puerta de Hierro de Majadahonda
Majadahonda, Madrid, 28222
Hospital Universitario Virgen de la Macarena
Seville, 41009
Consorcio Hospital General Universitario de Valencia
Valencia, 46014
Hospital Universitario y Politecnico La Fe
Valencia, 46026
Italy8 sites
AOU Policlinico Sant'Orsola Malpighi
Bologna, BO, 40138
Universita' degli Studi G. D'Annunzio -CeSi-MeT
Chieti, CH, 66100
Azienda Ospedaliero Universitaria San Martino di Genova
Genova, 16132
Ospedale Luigi Sacco
Milan, 20157
Prof. Giovanni Pellacani AOU Policlinico di Modena Struttura Complessa di Dermatologia
Modena, 41124
IFO Istituto Dermatologico San Gallicano IRCCS,
Roma, RM, 00144
Ospedale Cristo Re
Roma, ROME, 00167
Universita del Sacro Cuore, Policlinico Agostino Gemelli, Istituto Di Dermatologia
Rome, 00168
Slovakia8 sites
Fakultna Nemocnica s Poliklinikou F. D. Roosevelta Banska Bystrica
Banská Bystrica, 975 17
Narodny ustav detskych chorob, Detska dermatovenerologicka klinika LF UK a NUDCH
Bratislava, 833 40
BeneDerma s.r.o.
Bratislava, 841 02
Derma therapy spol. s.r.o, Dermatovenerologicka ambulancia
Bratislava, 85101
Pedi-Derma s.r.o., Dermatovenerologicka ambulancia
Košice, 04001
Nemocnica Kosice-Saca, a.s., 1. sukromna nemocnica, Kozna ambulancia
Kosice-Saca, 040 15
Derma-beauty, s.r.o., Dermatovenerologicka ambulancia
Nitra, 949 01
SANARE spol. s.r.o., Dermatovenerologicka ambulancia
Svidník, 089 01
Brazil7 sites
CETI - Centro de Estudos em Terapias Inovadoras LTDA.
Curitiba, Paraná, 80030-110
Hospital De Clinicas De Porto Alegre
Porto Alegre, Rio Grande do Sul, 90035-003
Associacao dos Funcionarios Públicos do Estado do Rio Grande do Sul - Hospital Ernesto Dornelles
Porto Alegre, Rio Grande do Sul, 90160-093
Instituto de Dermatologia e Estética do Brasil LTDA
Rio de Janeiro, Rio de Janeiro, 22470-220
IBPClin Pesquisa Clinica
Rio de Janeiro, 20241-180
Pesquisare Saude S/S Ltda
Santo André, São Paulo, 09.080-110
Fundacao do ABC - Faculdade de Medicina do ABC
Santo André, São Paulo, 09060-870
Bulgaria7 sites
MC Asklepii" OOD
Dupnitsa, 2600
MHAT "Dr. Tota Venkova" AD
Gabrovo, 5300
"Center of skin-venereal diseases" EOOD, Sofia
Sofia, 1404
"DCC Fokus-5-Medical Establishment for OutpatientCare"EOOD
Sofia, 1463
"Mc Sinexus Sofia" Eood
Sofia, 1784
ACIBADEM City Clinic Diagnostic-Consultative Center EOOD
Sofia, 1784
"ACIBADEM City Clinic Medical Center Varna" EOOD
Varna, 9000
Argentina6 sites
Psoriahue Medicina Interdisciplinaria
C.a.b.a, C1425DKG
CINME Centro de Investigaciones Metabolicas
C.a.b.a., C1027AAP
Buenos Aires Skin
C.a.b.a., C1055AAO
Framingham Centro Medico
La Plata, Buenos Aires, B1902COS
Hospital Universitario Austral
Pilar, Buenos Aires, B1629ODT
Servicio de Investigacion de Patolog-ias Alergicas del Instituto ABC
Rosario, Santa Fe Province, 2000
Mexico6 sites
Derma Norte del Bajio S.C
Aguascalientes, 20127
Centro de Investigacion Integral Medivest S.C.
Chihuahua City, 31203
Arke Estudios Clinicos S.A. de C.V.
Cuauhtémoc, Mexico City, 06700
Phylasis Clinicas Research S. de R.L. de C.V.
Cuautitlán Izcalli, State of Mexico, 54769
JM Research SC
Cuernavaca, Morelos, 62290
Centro de Dermatologia de Monterrey
Monterrey, Nuevo León, 64460
Taiwan6 sites
Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung City, 807
Taipei Medical University-Shuang Ho Hospital
New Taipei City, 23561
Chung Shan Medical University Hospital
Taichung, R.O.C 402
National Cheng-Kung University Hospital
Tainan, 704
National Taiwan University Hospital
Taipei, 100
Chang Gung Memorial Hospital Linkou Branch
Taoyuan City, 333
Israel5 sites
Soroka University Medical Center
Beersheba, 8410101
Rambam Health Care Campus
Haifa, 3109601
Rabin Medical Center
Petah Tikva, 4941492
The Chaim Sheba Medical Center
Ramat Gan, 5265601
Tel-Aviv Sourasky Medical Center
Tel Aviv, 6423906
Chile4 sites
Centro Medico SkinMed Limitada
Santiago, Santiago Metropolitan, 7580206
Clinica Dermacross S.A.
Santiago, Santiago Metropolitan, 7640881
Hospital Clinico Universidad de Chile
Santiago, Santiago Metropolitan, 8380456
Centro Internacional de Estudios Clinicos - CIEC
Santiago, Santiago Metropolitan, 8420383
Latvia4 sites
Riga 1st Hospital, Clinic of Dermatology and STD
Riga, LV - 1001
Health and Aesthetics Ltd
Riga, LV-1009
Health Centre 4 Ltd, Dermatology Clinics
Riga, LV-1013
Outpatient Clinic Of Ventspils
Ventspils, LV3601
Belgium3 sites
University Hospital Brussels
Brussels, 1090
Cliniques Universitaires Saint-Luc
Brussels, 1200
University Hospital Antwerp
Edegem, 2650
Romania3 sites
SC Centrul Medical de Diagnostic si Tratament Ambulator Neomed SRL
Brasov, JUD. Brasov, 500283
SC Delta Health Care SRL
Bucharest, 014142
Cabinet Medical de Dermatovenerologie Prof. Dr. Orasan Remus Ioan
Cluj-Napoca, JUD. CLUJ, 400105
Serbia3 sites
Military Medical Academy
Belgrade, 11000
Clinical Centre Nis
Niš, 18000
General Hospital Pancevo
Pančevo, 26000
Netherlands1 site
Universitair Medisch Centrum (UMC) Utrecht
Utrecht, 3584 CX
About this study
Official title: A PHASE 3 RANDOMIZED WITHDRAWAL, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER STUDY INVESTIGATING THE EFFICACY AND SAFETY OF PF-04965842 IN SUBJECTS AGED 12 YEARS AND OVER, WITH MODERATE TO SEVERE ATOPIC DERMATITIS WITH THE OPTION OF RESCUE TREATMENT IN FLARING SUBJECTS
B7451014 is a Phase 3 study to investigate PF-04965842 in patients aged 12 years and over with a minimum body weight of 40 kg who have moderate to severe atopic dermatitis. Subjects responding well to an initial open-label 12 week treatment of PF-04965842 (200 mg) taken orally once daily (QD) will be identified and randomized in a double-blind manner to receive 200 mg QD PF-04965842, 100 mg QD PF-04965842, or QD placebo. Efficacy and safety of 2 doses of PF-04965842 will be evaluated relative to placebo over 40 weeks. Subjects experiencing significant worsening of their symptoms, i.e., protocol-defined flare, enter 12 weeks rescue treatment and receive 200 mg PF-04965842 together with a marketed topical medicine. Eligible patients will have the option to enter a long-term extension study after completing the initial 12 week treatment, the 12 week rescue treatment, and the 40 week blinded treatment.
Read the detailed description
Responder criteria for randomization at week 12 are defined as a) achieving an IGA of clear (0) or almost clear (1) (on a 5 point scale), b) a reduction from IGA baseline of 2 or more points, and c) reaching an EASI-75 response compared to baseline. Flare requiring rescue treatment is defined as a loss of at least 50% of the EASI response at Week 12 and an IGA score of 2 or higher.
- Conditions
- Dermatitis, Dermatitis, Atopic, Eczema, Skin Diseases, Skin Diseases, Genetic, Genetic Diseases, Inborn
- Being tested
- PF-04965842 100 mg, PF-04965842 200 mg, Placebo
- Keywords
- atopic dermatitis, atopic eczema, eczema, JAK, janus kinase
- Medical subject headings
- Dermatitis, Dermatitis, Atopic, Eczema, Skin Diseases, Skin Diseases, Genetic, Genetic Diseases, Inborn, Skin Diseases, Eczematous, Hypersensitivity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PF-04965842 100 mgDrug
Also called Abrocitinib
PF-04965842 100 mg, administered as two tablets to be taken orally once daily for 40 weeks
PF-04965842 200 mgDrug
Also called Abrocitinib
PF-04965842 200 mg, administered as two tablets to be taken orally once daily for 40 weeks
PlaceboDrug
Placebo, administered as two tablets to be taken orally once daily for 40 weeks
| Study group | Role | What they receive |
|---|---|---|
| PF-04965842 100 mg QD | Experimental | Double-blind randomized treatment following open label run-in period. Receives: Drug: PF-04965842 100 mg |
| PF-04965842 200 mg QD | Experimental | Double-blind randomized treatment following open label run-in period. Receives: Drug: PF-04965842 200 mg |
| Placebo QD | Placebo comparator | Double-blind randomized treatment following open label run-in period. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants With Loss of Response: Double-blind (DB) Period
Percentage of participants with loss of response requiring rescue treatment during double blind period was determined. Loss of response denoted as flare and was define as a loss of at least 50% of EASI total score at Week 12 and with an IGA score of 2 or higher. EASI quantifies severity of participant's atopic dermatitis (AD) based on both severity of lesion clinical signs and % of body surface area (BSA) affected. EASI is a composite scoring by AD clinical evaluator of degree of erythema, induration/papulation, excoriation, and lichenification for each of 4 body regions. EASI total score range from 0.0 to 72.0, with higher scores representing greater severity of AD. IGA assesses severity of AD on 5-point scale (0 to 4, higher scores = more severity), reflecting global consideration of erythema, induration and scaling. Where, 0 = clear; 1 = almost clear; 2 = mild; 3 = moderate and 4 = severe.
Measured: From Day 1 of up to Week 40 of double blind period
Time to Loss of Response: Double-blind Period
Time (in days) to loss of response based on achieving IGA >=2 was measured from date of first dose of randomized treatment until last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) and based on EASI, loss of at least 50% of EASI response at Week 12 and IGA score of 2 or higher. IGA assesses severity of AD on 5-point scale (0 to 4, higher scores=more severity), reflecting global consideration of erythema, induration and scaling with scores 0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe. EASI quantifies severity of AD based on severity of lesion clinical signs and % of BSA affected. EASI composite score evaluates degree of erythema, induration/papulation, excoriation, and lichenification.
Measured: From date of first dose of randomized treatment until the last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) (maximum up to Week 40, visit window was extended +/- 45 Days due to COVID 19)
Secondary outcomes (26)
Time to First Loss of Response Based on Investigator's Global Assessment (IGA) Score of 2 or Higher: Double-blind Period
Time (in days) to loss of response based on achieving IGA >=2 (for the first time) as measured from date of first dose of randomized treatment until the last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue). IGA assesses severity of AD on a 5-point scale (0 to 4, higher scores indicated more severity), reflecting global consideration of erythema, induration and scaling. Where, 0 = clear, AD is cleared; 1 = almost clear, AD not entirely cleared, light pink residual lesions; 2 = mild, AD with light red lesions; 3 = moderate, AD with red lesions; 4 = severe, AD with deep, dark red lesions.
Measured: From date of first dose of randomized treatment until the last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) (maximum up to Week 40, visit window +/- 7 Days)
Percentage of Participants Achieving Investigator's Global Assessment (IGA) Response of Clear (0) or Almost Clear (1) and a Reduction of Greater Than or Equal to (>=) 2 Points From Baseline at Weeks 12, 16, 28, 40, and 52: Double-blind Period
IGA assessed severity of AD on a 5-point scale (0 to 4, higher scores indicated more severity), reflecting global consideration of erythema, induration and scaling. Where, 0 = clear, AD is cleared; 1 = almost clear, AD not entirely cleared, light pink residual lesions; 2 = mild, AD with light red lesions; 3 = moderate, AD with red lesions; 4 = severe, AD with deep dark red lesions.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=50% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
EASI quantifies severity of participant's AD (excluded scalp, palms, soles) based on severity of AD clinical signs and % of BSA affected. Severity of clinical signs of AD (erythema [E], induration/papulation [I], excoriation [Ex] and lichenification [L]) was scored separately for each of 4 body regions (head and neck [h], upper limbs [u], trunk [t] [including axillae and groin] and lower limbs [l] [including buttocks]) on 4-point scale: 0 = absent; 1 = mild; 2 = moderate; 3 = severe. EASI area score was based upon % BSA with AD in body region: 0 (0%), 1 (>0 to <10%), 2 (10 to <30%), 3 (30 to <50%), 4 (50 to <70%), 5 (70 to <90%) and 6 (90 to 100%). Total EASI score = 0.1*Ah*(Eh+Ih+Exh+Lh) + 0.2*Au*(Eu+Iu+ExU+Lu) + 0.3*At*(Et+It+Ext+Lt) + 0.4*Al*(El+Il+Exl+Ll); where A = area score. Total EASI score ranged from 0.0 to 72.0, higher scores = greater severity of AD.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=75% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
EASI quantifies severity of participant's AD (excluded scalp, palms, soles) based on severity of AD clinical signs and % of BSA affected. Severity of clinical signs of AD (erythema, induration/papulation, excoriation and lichenification) scored separately for each of 4 body regions (head and neck, upper limbs, trunk [including axillae and groin] and lower limbs [including buttocks]) on 4-point scale: 0 = absent; 1 = mild; 2 = moderate; 3 = severe. EASI area score was based upon % BSA with AD in body region: 0 (0%), 1 (>0 to <10%), 2 (10 to <30%), 3 (30 to <50%), 4 (50 to <70%), 5 (70 to <90%) and 6 (90 to 100%). Total EASI score = 0.1*Ah*(Eh+Ih+Exh+Lh) + 0.2*Au*(Eu+Iu+ExU+Lu) + 0.3*At*(Et+It+Ext+Lt) + 0.4*Al*(El+Il+Exl+Ll). Total EASI score ranged from 0.0 to 72.0, higher scores = greater severity of AD.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=90% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
EASI quantifies severity of participant's AD (excluded scalp, palms, soles) based on severity of AD clinical signs and % of BSA affected. Severity of clinical signs of AD (erythema, induration/papulation, excoriation and lichenification) scored separately for each of 4 body regions (head and neck, upper limbs, trunk [including axillae and groin] and lower limbs [including buttocks]) on 4-point scale: 0 = absent; 1 = mild; 2 = moderate; 3 = severe. EASI area score was based upon % BSA with AD in body region: 0 (0%), 1 (>0 to <10%), 2 (10 to <30%), 3 (30 to <50%), 4 (50 to <70%), 5 (70 to <90%) and 6 (90 to 100%). Total EASI score = 0.1*Ah*(Eh+Ih+Exh+Lh) + 0.2*Au*(Eu+Iu+ExU+Lu) + 0.3*At*(Et+It+Ext+Lt) + 0.4*Al*(El+Il+Exl+Ll). Total EASI score ranged from 0.0 to 72.0, higher scores=greater severity of AD.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=100% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
EASI quantifies severity of participant's AD (excluded scalp, palms, soles) based on severity of AD clinical signs and % of BSA affected. Severity of clinical signs of AD (erythema, induration/papulation, excoriation and lichenification) scored separately for each of 4 body regions (head and neck, upper limbs, trunk [including axillae and groin] and lower limbs [including buttocks]) on 4-point scale: 0= absent; 1= mild; 2= moderate; 3= severe. EASI area score was based upon % BSA with AD in body region: 0 (0%), 1 (>0 to <10%), 2 (10 to <30%), 3 (30 to <50%), 4 (50 to <70%), 5 (70 to <90%) and 6 (90 to 100%). Total EASI score =0.1*Ah*(Eh+Ih+Exh+Lh) + 0.2*Au*(Eu+Iu+ExU+Lu) + 0.3*At*(Et+It+Ext+Lt) + 0.4*Al*(El+Il+Exl+Ll). Total EASI score ranged from 0.0 to 72.0, higher scores=greater severity of AD.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With Greater Than or Equal 4 Points Improvement in the Numerical Rating Scale (NRS) for Severity of Pruritus From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Participants were asked to assess their worst itching due to AD over the past 24 hours on an NRS scale ranged from 0 (no itch) to 10 (worst itch imaginable), where higher scores indicated worse disease status.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percent Change From Baseline in Body Surface Area (BSA) at Weeks 12, 16, 28, 40 and 52: Double-blind Period
4 body regions evaluated: head and neck, upper limbs, trunk (including axillae, groin/genitals), lower limbs (including buttocks) excluding scalp, palms, soles. BSA calculated by handprint method. Number (No) of handprints (size of participant's hand with fingers in closed position) fitting in affected area of a body region was estimated. Maximum No of handprints were 10, 20, 30, 40 for head and neck, upper limbs, trunk, and lower limbs respectively. Surface area (SA) of body region equivalent to 1 handprint: 1 handprint=10% for head and neck, 5% for upper limbs, 3.33% for trunk and 2.5% for lower limbs. %Change BSA for a body region was calculated as=total No of handprints in a body region* %SA equivalent to 1 handprint. %BSA for an individual: arithmetic mean of %BSA of all 4 body regions, ranged from 0-100%, higher values=greater AD severity.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percent Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Total Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3); severity scores added to give B (0-18). C: pruritus and sleep loss, each of these 2 were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Visual Analogue Scale (VAS) of Itch and Sleep Loss at Weeks 12, 16, 28, 40 and 52: Double-blind Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region-head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With >=50% Improvement From Baseline in Scoring Atopic Dermatitis (SCORAD) Response at Weeks 12, 16, 28, 40 and 52: Double-blind Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With >=75% Improvement From Baseline in Scoring Atopic Dermatitis (SCORAD) Response at Weeks 12, 16, 28, 40 and 52: Double-blind Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving IGA Response of Clear (0) or Almost Clear (1) and Greater Than or Equal to (>=) 2 Points Improvement From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
IGA assessed severity of AD on a 5-point scale (0-4, higher scores indicated more severity), reflecting global consideration of erythema, induration and scaling. Where, 0=clear, AD is cleared; 1 = almost clear, AD not entirely cleared, light pink residual lesions; 2 = mild, AD with light red lesions; 3 = moderate, AD with red lesions; 4 = severe, AD with deep, dark red lesions.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Total Eczema Area and Severity Index (EASI) Score at Rescue Weeks 2, 4, 8 and 12: Rescue Period
EASI quantifies severity of participant's AD (excluded scalp, palms, soles) based on severity of AD clinical signs and % of BSA affected. Severity of clinical signs of AD (erythema, induration/papulation, excoriation and lichenification) scored separately for each of 4 body regions (head and neck, upper limbs, trunk [including axillae and groin] and lower limbs [including buttocks]) on 4-point scale: 0= absent; 1= mild; 2= moderate; 3= severe. EASI area score was based upon % BSA with AD in body region: 0 (0%), 1 (>0 to <10%), 2 (10 to <30%), 3 (30 to <50%), 4 (50 to <70%), 5 (70 to <90%) and 6 (90 to 100%). Total EASI score =0.1*Ah*(Eh+Ih+Exh+Lh) + 0.2*Au*(Eu+Iu+ExU+Lu) + 0.3*At*(Et+It+Ext+Lt) + 0.4*Al*(El+Il+Exl+Ll). Total EASI score ranged from 0.0 to 72.0, higher scores=greater severity of AD.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants Achieving Greater Than or Equal to 4 Points Improvement From Rescue Baseline in Peak Pruritus Numeric Rating Scale (PP-NRS) at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Participants were asked to assess their worst itching due to AD over the past 24 hours on an NRS scale ranged from 0 (no itch) to 10 (worst itch imaginable), where higher scores indicated greater severity.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Percent Body Surface Area (BSA) at Rescue Weeks 2, 4, 8 and 12: Rescue Period
4 body regions were evaluated: head and neck, upper limbs, trunk (including axillae and groin/genitals) and lower limbs (including buttocks). Scalp, palms and soles were excluded. BSA was calculated using handprint method. Number of handprints (size of participant's hand with fingers in a closed position) fitting in affected area of a body region was estimated. Maximum number of handprints were 10 for head and neck, 20 for upper limbs, 30 for trunk and 40 for lower limbs. Surface area of body region equivalent to 1 handprint: 1 handprint was equal to 10% for head and neck, 5% for upper limbs, 3.33% for trunk and 2.5% for lower limbs. Overall % BSA for an individual % BSA of all 4 body regions, ranged from 0 to 100%, with higher values representing greater severity of AD.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Scoring Atopic Dermatitis (SCORAD) Visual Analog Scale (VAS) Score of Itch and Sleep Loss at Rescue Weeks 2, 4, 8 and 12: Rescue Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants With 50% Improvement in Scoring Atopic Dermatitis (SCORAD) From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants With 75% Improvement in Scoring Atopic Dermatitis (SCORAD) From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
SCORAD: scoring index for AD combining extent (A), severity (B), subjective symptoms (C). A: rule of 9 used to calculate BSA affected by AD as % of whole BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; genitals 1%. Score of each body region added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; skin thickening; dryness) was assessed as none (0), mild (1), moderate (2), severe (3). Severity scores added to give B (0-18). C: pruritus and sleep loss, each were scored by participant/caregiver using VAS where, 0=no itch/no sleep loss and 10=worst imaginable itch/sleep loss, higher scores=worse symptoms. Scores for itch and sleep loss added to give 'C' (0-20). SCORAD calculated as: A/5+7*B/2+C; range (0-103); higher values=worse outcome.
Measured: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants Achieving Patient Global Assessment (PtGA) Response of 'Clear (0)' or 'Almost Clear (1)' and Greater Than or Equal to 2 Points Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Participant responded to the following question: "Overall, how would you describe your Atopic Dermatitis right now?" on a 5-point scale: 0= clear; 1= almost clear; 2= mild; 3= moderate; and 4= severe. Higher scores indicated more severity.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Dermatology Life Quality Index (DLQI) Score for Adults at Weeks 12, 16, 28, 40 and 52: Double-blind Period
DLQI was a 10-item questionnaire that measures the impact of skin disease. Each question was evaluated on a 4-point scale (range 0 to 3) where, 0 = not at all, 1= a little, 2= a lot, 3= very much, where higher scores indicated more impact on quality of life. Scores from all 10 questions were added up to give DLQI total score range from 0 (not at all) to 30 (very much). Higher scores indicated more impact on quality of life of participants.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Children's Dermatology Life Quality Index (CDLQI) Score for Adolescents at Weeks 12, 16, 28, 40 and 52: Double-blind Period
CDLQI is a 10-item questionnaire that measures the impact of skin disease on adolescents (aged 12-17 years) quality of life over the last week. Each question was evaluated on a 4-point scale (range 0 to 3) where, 0 = not at all , 1 = only a little, 2 = quite a lot, 3 = very much, where higher scores indicated more impact on quality of life. Scores from all 10 questions were added up to give CDLQI total score range from 0 (not at all) to 30 (very much). Higher scores indicated more impact on quality of life of children.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Hospital Anxiety and Depression Scale (HADS) - Anxiety Scale at Weeks 12, 16, 28, 40 and 52: Double-blind Period
HADS: participant rated 14-item questionnaire. HADS consisted of 2 subscales: HADS-Anxiety (HADS-A) scale and HADS-Depression (HADS-D) scale, both of these subscales comprised of 7 items each. Each item was rated on a 4-point scale, score range from 0 to 3, where higher scores indicates more anxiety/depression symptoms. HADS-A assesses state of generalized anxiety (anxious mood, restlessness, anxious thoughts, panic attacks). HADS-A: sum of all 7 items resulted in score range of 0 (no presence of anxiety) to 21 (severe feeling of anxiety); higher score indicating greater severity of anxiety.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Hospital Anxiety and Depression Scale (HADS) - Depression Scale at Weeks 12, 16, 28, 40 and 52: Double-blind Period
HADS: participant rated 14-item questionnaire. HADS consisted of 2 subscales: HADS-A scale and HADS-D scale, both of these subscales comprised of 7 items each. Each item was rated on a 4-point scale, score range from 0 to 3, where higher scores indicates more anxiety/depression symptoms. HADS-D assesses state of lost interest and diminished pleasure response (lowering of hedonic tone). HADS-D: sum of all 7 items resulted in score range of 0 (no presence of depression) to 21 (severe feeling of depression); higher score indicating greater severity of depression symptoms.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Patient Oriented Eczema Measure (POEM) Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
POEM was a 7-item participant reported outcome (PRO) measure used to assess the impact of AD (dryness, itching, flaking, cracking, sleep loss, bleeding and weeping) over the past week. Each item scored as following: no days = 0, 1-2 days = 1, 3-4 days = 2, 5-6 days = 3 and, every day = 4. The total POEM score ranges from 0 to 28, where higher score indicated greater severity.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Pruritus and Symptoms Assessment for Atopic Dermatitis (PSAAD) Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
PSAAD is a daily participant reported symptom electronic diary. Participants rated their symptoms of AD over the past 24 hours, using 11 items (itchy skin, painful skin, dry skin, flaky skin, cracked skin, bumpy skin, red skin, discolored skin [darker or lighter], bleeding from skin, seeping or oozing fluid from skin [other than blood], and skin swelling). Participants had to think about all the areas of their body affected by their skin condition and chose the number that best described their experience for each of the 11 items, from 0 (no symptoms) to 10 (extreme symptoms), higher scores signified worse skin condition. Total PSAAD score = arithmetic mean of 11 items, 0 (no symptoms) to 10 (extreme symptoms), where higher score = worse skin condition.
Measured: Baseline, Weeks 12, 16, 28, 40 and 52
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Aug 2018
- Study start11 Jun 2018
- Primary completion2 Sep 2020
- Study completion7 Oct 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (7)Papers the sponsor has linked to this study.
- Other trials for DermatitisStudies of the same condition, open and under way.
- More trials run by PfizerThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 1,235 participants (actual)
Sponsor and investigators
- Lead sponsor
- Pfizer
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Pfizer CT.gov Call Center, Study director, Pfizer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03627767
- Sponsor's protocol ID
- B7451014
- Other IDs
- JADE REGIMEN, 2018-000501-23, REGIMEN, 2018
- Status last verified
- Sep 2021
- First submitted
- 29 May 2018
- Last updated
- 20 Sep 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.
Publications
Guttman-Yassky E, Bieber T, Kabashima K, Gutermuth J, Weidinger S, Wollenberg A, Lazariciu I, Encinas G, Mikheil M, Watkins M. Sustained on/off-treatment disease control with abrocitinib for moderate-to-severe atopic dermatitis. J Dermatolog Treat. 2026 Dec;37(1):2672328. doi: 10.1080/09546634.2026.2672328. Epub 2026 May 21.
PubMed 42165315Silverberg JI, Simpson EL, Farooqui SA, Chan G, Biswas P, Guler E. Efficacy and Safety of Variable-Dose Versus Continuous-Dose Abrocitinib Treatment in Patients with Moderate-to-Severe Atopic Dermatitis: A Pooled Analysis. Dermatol Ther (Heidelb). 2026 May 20. doi: 10.1007/s13555-026-01778-y. Online ahead of print.
PubMed 42162528Paller AS, Eichenfield LF, Irvine AD, Flohr C, Wollenberg A, Barbarot S, Bangert C, Spergel JM, Selfridge A, Biswas P, Fan H, Alderfer J, Watkins M, Koppensteiner H. Integrated Efficacy and Safety Analysis of Abrocitinib in Adolescents With Moderate-to-Severe Atopic Dermatitis. Allergy. 2025 Aug;80(8):2213-2224. doi: 10.1111/all.16512. Epub 2025 Mar 3.
PubMed 40028832Armstrong AW, Alexis AF, Blauvelt A, Silverberg JI, Feeney C, Levenberg M, Chan G, Zhang F, Fostvedt L. Predicting Abrocitinib Efficacy at Week 12 Based on Clinical Response at Week 4: A Post Hoc Analysis of Four Randomized Studies in Moderate-to-Severe Atopic Dermatitis. Dermatol Ther (Heidelb). 2024 Jul;14(7):1849-1861. doi: 10.1007/s13555-024-01183-3. Epub 2024 Jun 19.
PubMed 38896380Flohr C, Cork MJ, Ardern-Jones MR, Eichenfield LF, Barbarot S, Feeney C, Rojo R, Lazariciu I, Nesnas J. Efficacy and safety of abrocitinib monotherapy in adolescents and adults: a post hoc analysis of the phase 3 JAK1 atopic dermatitis efficacy and safety (JADE) REGIMEN clinical trial. J Dermatolog Treat. 2023 Dec;34(1):2200866. doi: 10.1080/09546634.2023.2200866.
PubMed 37036183Wojciechowski J, Malhotra BK, Wang X, Fostvedt L, Valdez H, Nicholas T. Population pharmacokinetic-pharmacodynamic modelling of platelet time-courses following administration of abrocitinib. Br J Clin Pharmacol. 2022 Aug;88(8):3856-3871. doi: 10.1111/bcp.15334. Epub 2022 Apr 11.
PubMed 35342978Simpson EL, Silverberg JI, Nosbaum A, Winthrop KL, Guttman-Yassky E, Hoffmeister KM, Egeberg A, Valdez H, Zhang M, Farooqui SA, Romero W, Thorpe AJ, Rojo R, Johnson S. Integrated Safety Analysis of Abrocitinib for the Treatment of Moderate-to-Severe Atopic Dermatitis From the Phase II and Phase III Clinical Trial Program. Am J Clin Dermatol. 2021 Sep;22(5):693-707. doi: 10.1007/s40257-021-00618-3. Epub 2021 Aug 18.
PubMed 34406619
Study at a glance
From the registry record, last updated by the sponsor on 20 Sep 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A PHASE 3 RANDOMIZED WITHDRAWAL, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER STUDY INVESTIGATING THE EFFICACY AND SAFETY OF PF-04965842 IN SUBJECTS AGED 12 YEARS AND OVER, WITH MODERATE TO SEVERE ATOPIC DERMATITIS WITH THE OPTION OF RESCUE TREATMENT IN FLARING SUBJECTS
- ClinicalTrials.gov ID
- NCT03627767
- Acronym / sponsor ID
- B7451014
- Conditions
- Dermatitis, Dermatitis, Atopic, Eczema, Skin Diseases, Skin Diseases, Genetic, Genetic Diseases, Inborn
- Keywords
- atopic dermatitis, atopic eczema, eczema, JAK, janus kinase
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,235 participants (actual)
- Lead sponsor
- PfizerIndustry (pharma, biotech, devices)
- Study start
- 11 Jun 2018 (actual)
- Primary completion
- 2 Sep 2020 (actual)
- Study completion
- 7 Oct 2020 (actual)
- First posted
- 13 Aug 2018 (actual)
- Results
- Posted 20 Sep 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
B7451014 is a Phase 3 study to investigate PF-04965842 in patients aged 12 years and over with a minimum body weight of 40 kg who have moderate to severe atopic dermatitis. Subjects responding well to an initial open-label 12 week treatment of PF-04965842 (200 mg) taken orally once daily (QD) will be identified and randomized in a double-blind manner to receive 200 mg QD PF-04965842, 100 mg QD PF-04965842, or QD placebo. Efficacy and safety of 2 doses of PF-04965842 will be evaluated relative to placebo over 40 weeks. Subjects experiencing significant worsening of their symptoms, i.e., protocol-defined flare, enter 12 weeks rescue treatment and receive 200 mg PF-04965842 together with a marketed topical medicine. Eligible patients will have the option to enter a long-term extension study after completing the initial 12 week treatment, the 12 week rescue treatment, and the 40 week blinded treatment.
Detailed description
Responder criteria for randomization at week 12 are defined as a) achieving an IGA of clear (0) or almost clear (1) (on a 5 point scale), b) a reduction from IGA baseline of 2 or more points, and c) reaching an EASI-75 response compared to baseline. Flare requiring rescue treatment is defined as a loss of at least 50% of the EASI response at Week 12 and an IGA score of 2 or higher.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| PF-04965842 100 mg QD | Experimental | Drug: PF-04965842 100 mgDouble-blind randomized treatment following open label run-in period. |
| PF-04965842 200 mg QD | Experimental | Drug: PF-04965842 200 mgDouble-blind randomized treatment following open label run-in period. |
| Placebo QD | Placebo comparator | Drug: PlaceboDouble-blind randomized treatment following open label run-in period. |
Who may qualify
- Ages
- 12 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- 12 years of age or older with a minimum body weight of 40 kg
- Diagnosis of atopic dermatitis (AD) for at least 1 year and current status of moderate to severe disease (>= the following scores: BSA10%, IGA 3, EASI 16, Pruritus NRS 4)
- Recent history of inadequate response or inability to tolerate topical AD treatments or require systemic treatments for AD control
Key exclusion criteria (5 listed)
- Unwilling to discontinue current AD medications prior to the study or require treatment with prohibited medications during the study
- Prior treatment with JAK inhibitors
- Other active nonAD inflammatory skin diseases or conditions affecting skin
- Medical history including thrombocytopenia, coagulopathy or platelet dysfunction, Q wave interval abnormalities, current or history of certain infections, cancer, lymphoproliferative disorders and other medical conditions at the discretion of the investigator
- Pregnant or breastfeeding women, or women of childbearing potential who are unwilling to use contraception
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PF-04965842 100 mgAlso: AbrocitinibPF-04965842 100 mg, administered as two tablets to be taken orally once daily for 40 weeks | Drug | PF-04965842 100 mg QD |
| PF-04965842 200 mgAlso: AbrocitinibPF-04965842 200 mg, administered as two tablets to be taken orally once daily for 40 weeks | Drug | PF-04965842 200 mg QD |
| PlaceboPlacebo, administered as two tablets to be taken orally once daily for 40 weeks | Drug | Placebo QD |
Primary outcome
Percentage of Participants With Loss of Response: Double-blind (DB) Period
Time frame: From Day 1 of up to Week 40 of double blind period
Percentage of participants with loss of response requiring rescue treatment during double blind period was determined. Loss of response denoted as flare and was define as a loss of at least 50% of EASI total score at Week 12 and with an IGA score of 2 or higher. EASI quantifies severity of participant's atopic dermatitis (AD) based on both severity of lesion clinical signs and % of body surface area (BSA) affected. EASI is a composite scoring by AD clinical evaluator of degree of erythema, induration/papulation, excoriation, and lichenification for each of 4 body regions. EASI total score range from 0.0 to 72.0, with higher scores representing greater severity of AD. IGA assesses severity of AD on 5-point scale (0 to 4, higher scores = more severity), reflecting global consideration of erythema, induration and scaling. Where, 0 = clear; 1 = almost clear; 2 = mild; 3 = moderate and 4 = severe.
Time to Loss of Response: Double-blind Period
Time frame: From date of first dose of randomized treatment until the last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) (maximum up to Week 40, visit window was extended +/- 45 Days due to COVID 19)
Time (in days) to loss of response based on achieving IGA >=2 was measured from date of first dose of randomized treatment until last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) and based on EASI, loss of at least 50% of EASI response at Week 12 and IGA score of 2 or higher. IGA assesses severity of AD on 5-point scale (0 to 4, higher scores=more severity), reflecting global consideration of erythema, induration and scaling with scores 0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe. EASI quantifies severity of AD based on severity of lesion clinical signs and % of BSA affected. EASI composite score evaluates degree of erythema, induration/papulation, excoriation, and lichenification.
26 secondary outcomes
Time to First Loss of Response Based on Investigator's Global Assessment (IGA) Score of 2 or Higher: Double-blind Period
Time frame: From date of first dose of randomized treatment until the last dose of randomized treatment (if not entered rescue) or first day of rescue treatment (if entered rescue) (maximum up to Week 40, visit window +/- 7 Days)
Percentage of Participants Achieving Investigator's Global Assessment (IGA) Response of Clear (0) or Almost Clear (1) and a Reduction of Greater Than or Equal to (>=) 2 Points From Baseline at Weeks 12, 16, 28, 40, and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=50% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=75% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=90% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving Eczema Area and Severity Index (EASI) Response >=100% Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With Greater Than or Equal 4 Points Improvement in the Numerical Rating Scale (NRS) for Severity of Pruritus From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percent Change From Baseline in Body Surface Area (BSA) at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percent Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Total Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Visual Analogue Scale (VAS) of Itch and Sleep Loss at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With >=50% Improvement From Baseline in Scoring Atopic Dermatitis (SCORAD) Response at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants With >=75% Improvement From Baseline in Scoring Atopic Dermatitis (SCORAD) Response at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Percentage of Participants Achieving IGA Response of Clear (0) or Almost Clear (1) and Greater Than or Equal to (>=) 2 Points Improvement From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Total Eczema Area and Severity Index (EASI) Score at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants Achieving Greater Than or Equal to 4 Points Improvement From Rescue Baseline in Peak Pruritus Numeric Rating Scale (PP-NRS) at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Percent Body Surface Area (BSA) at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percent Change From Rescue Baseline in Scoring Atopic Dermatitis (SCORAD) Visual Analog Scale (VAS) Score of Itch and Sleep Loss at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants With 50% Improvement in Scoring Atopic Dermatitis (SCORAD) From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants With 75% Improvement in Scoring Atopic Dermatitis (SCORAD) From Rescue Baseline at Rescue Weeks 2, 4, 8 and 12: Rescue Period
Time frame: Rescue Baseline: last observation collected between last dose of blinded treatment and Day 1 (first dose day) of rescue treatment, Rescue Weeks 2, 4, 8 and 12
Percentage of Participants Achieving Patient Global Assessment (PtGA) Response of 'Clear (0)' or 'Almost Clear (1)' and Greater Than or Equal to 2 Points Improvement From Baseline at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Dermatology Life Quality Index (DLQI) Score for Adults at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Children's Dermatology Life Quality Index (CDLQI) Score for Adolescents at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Hospital Anxiety and Depression Scale (HADS) - Anxiety Scale at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Hospital Anxiety and Depression Scale (HADS) - Depression Scale at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Patient Oriented Eczema Measure (POEM) Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Change From Baseline in Pruritus and Symptoms Assessment for Atopic Dermatitis (PSAAD) Score at Weeks 12, 16, 28, 40 and 52: Double-blind Period
Time frame: Baseline, Weeks 12, 16, 28, 40 and 52
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Sep 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 42165315Guttman-Yassky E, Bieber T, Kabashima K, Gutermuth J, Weidinger S, Wollenberg A, Lazariciu I, Encinas G, Mikheil M, Watkins M. Sustained on/off-treatment disease control with abrocitinib for moderate-to-severe atopic dermatitis. J Dermatolog Treat. 2026 Dec;37(1):2672328. doi: 10.1080/09546634.2026.2672328. Epub 2026 May 21.
- Derived from this study: PubMed 42162528Silverberg JI, Simpson EL, Farooqui SA, Chan G, Biswas P, Guler E. Efficacy and Safety of Variable-Dose Versus Continuous-Dose Abrocitinib Treatment in Patients with Moderate-to-Severe Atopic Dermatitis: A Pooled Analysis. Dermatol Ther (Heidelb). 2026 May 20. doi: 10.1007/s13555-026-01778-y. Online ahead of print.
- Derived from this study: PubMed 40028832Paller AS, Eichenfield LF, Irvine AD, Flohr C, Wollenberg A, Barbarot S, Bangert C, Spergel JM, Selfridge A, Biswas P, Fan H, Alderfer J, Watkins M, Koppensteiner H. Integrated Efficacy and Safety Analysis of Abrocitinib in Adolescents With Moderate-to-Severe Atopic Dermatitis. Allergy. 2025 Aug;80(8):2213-2224. doi: 10.1111/all.16512. Epub 2025 Mar 3.
- Derived from this study: PubMed 38896380Armstrong AW, Alexis AF, Blauvelt A, Silverberg JI, Feeney C, Levenberg M, Chan G, Zhang F, Fostvedt L. Predicting Abrocitinib Efficacy at Week 12 Based on Clinical Response at Week 4: A Post Hoc Analysis of Four Randomized Studies in Moderate-to-Severe Atopic Dermatitis. Dermatol Ther (Heidelb). 2024 Jul;14(7):1849-1861. doi: 10.1007/s13555-024-01183-3. Epub 2024 Jun 19.
- Derived from this study: PubMed 37036183Flohr C, Cork MJ, Ardern-Jones MR, Eichenfield LF, Barbarot S, Feeney C, Rojo R, Lazariciu I, Nesnas J. Efficacy and safety of abrocitinib monotherapy in adolescents and adults: a post hoc analysis of the phase 3 JAK1 atopic dermatitis efficacy and safety (JADE) REGIMEN clinical trial. J Dermatolog Treat. 2023 Dec;34(1):2200866. doi: 10.1080/09546634.2023.2200866.
- Derived from this study: PubMed 35342978Wojciechowski J, Malhotra BK, Wang X, Fostvedt L, Valdez H, Nicholas T. Population pharmacokinetic-pharmacodynamic modelling of platelet time-courses following administration of abrocitinib. Br J Clin Pharmacol. 2022 Aug;88(8):3856-3871. doi: 10.1111/bcp.15334. Epub 2022 Apr 11.
- Derived from this study: PubMed 34406619Simpson EL, Silverberg JI, Nosbaum A, Winthrop KL, Guttman-Yassky E, Hoffmeister KM, Egeberg A, Valdez H, Zhang M, Farooqui SA, Romero W, Thorpe AJ, Rojo R, Johnson S. Integrated Safety Analysis of Abrocitinib for the Treatment of Moderate-to-Severe Atopic Dermatitis From the Phase II and Phase III Clinical Trial Program. Am J Clin Dermatol. 2021 Sep;22(5):693-707. doi: 10.1007/s40257-021-00618-3. Epub 2021 Aug 18.
- To obtain contact information for a study center near you, click here.Link provided by the sponsor.
- Individual participant dataSharing planned: Yes. Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pfizer CT.gov Call Center study director
Pfizer
235 sites in 21 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing PF-04965842 100 mg and PF-04965842 200 mg in people with Dermatitis and Dermatitis, Atopic, run by Pfizer at 235 sites in 21 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Sep 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 235 sites in United States, Poland, China, Germany, Canada and 16 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 20 Sep 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants With Loss of Response: Double-blind (DB) Period (time frame: From Day 1 of up to Week 40 of double blind period). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03627767, which also lists 7 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Sep 2021.