Dermatitis, AtopicNCT05250115
A Study to Learn About Abrocitinib in Adult Patients With Moderate to Severe Atopic Dermatitis
An observational study of Dermatitis, Atopic, run by Pfizer at 38 sites in Germany.
Trial summary
The purpose of this non-interventional observational study is to learn about the safety and effects of the medicinal product (called Abrocitinib) for the potential treatment of moderate to severe atopic dermatitis (AD). AD is a long-lasting disease that causes redness and irritation of the skin. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Dermatitis, Atopic
- How many people
- 112 participants
- Where
- 38 sitesGermany
- Study dates
- 10 May 2022to 25 Jul 2024
- How long will I take part?
- 12 Months
- Phase
- Observational
- 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 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: A prospective, single-arm, multi-center, observational non-interventional study looking at adult patients with moderate-severe atopic dermatitis, who have been chosen to start treatment with Abrocitinib in Germany according to the current routine practice of the treating physician.
Who may be able to join
- Patients aged ≥18 years
- Confirmed diagnosis of AD by dermatologist prior to study inclusion
- Patient for whom the decision to initiate treatment with abrocitinib was made as part of routine clinical practice irrespective of the patients being
- abrocitinib naive or,
- patients who reinitialize treatment with abrocitinib after being off treatment for ≥28 days prior to study inclusion
- Patient is eligible for abrocitinib treatment according to Summary of Product Characteristics (SmPC)
- Evidence of a personally signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the non-interventional study
Who cannot join
- Contraindications according to SmPC
- Receipt of any investigational drug within 3 months or longer if required according to wash-out period prior to inclusion or participation in a clinical trial during observation period
- Patients being treated with abrocitinib within a time period of <28 days prior to the timepoint of study inclusion
- Patients who are investigational site staff members or patients who are Pfizer employees directly involved in the conduct of the non-interventional study
- Patients who are unable to consent
Trial locations and contacts
38 sites in 1 country.
38 sites in 1 country
Germany38 sites
Hautärztliche Gemeinschaftspraxis
Ahaus, 48688
Hautarztpraxis Dr. Virgil Mihaescu
Augsburg, 86150
Dermatologie Bad Kreuznach - Dr. med. Georg Mauer
Bad Kreuznach, 55543
Praxis Dr. A. Magerl
Bensheim, 64625
Hautzentrum
Bergen, 18528
Dr. Christiane Handrick Hautarztpraxis
Berlin, 10117
Dres. Ziethen-Stavermann GbR
Berlin, 12353
Hautarztpraxis Dr. med. Thomas Schirmer
Berlin, 12489
Hautzentrum Weißensee
Berlin, 13086
Hautarztpraxis Weid
Bingen, 55411
Hautarztpraxis an der Hase Studienzentrum
Bramsche, 49565
Hautärzte Braunschweig
Braunschweig, 38114
Elbe Kliniken Stade - Buxtehude GmbH
Buxtehude, Lower Saxony, 21614
Hautarztpraxis Dr. med. Daniela Kasche
Buxtehude, 21614
Praxis Dr. Voth
Cologne, 50677
BAG Freitag und Knöll
Falkensee, 14612
Haut- und Laserzentrum Freisung Prof. Kurzen
Freising, 85354
ÜUeberoertliche Gemeinschaftspraxis Jost Kai Rietkoetter Robert Jablonka
Gelsenkirchen, North Rhine-Westphalia, 32423
Hautarztpraxis Dr. med Michael Loth
Gernsbach, 76593
Hautarztpraxis Dr. Brinkmann, Schult & Samimi-Fard
Gladbeck, 45964
Cutaneum Praxis Dr. Buck
Hamburg, 20095
Hautarztpraxis Dr. med. Matthias Lütten
Hamburg, 20095
Universitätsklinikum Hamburg-Eppendorf
Hamburg, 20246
dermaSANA
Karlsruhe, 76131
Kosmedikulm
Kulmbach, 95326
Dr. Beate Schwarz
Langenau, 89129
"Magdeburger company for Medical studies & Services"
Magdeburg, Saxony-Anhalt, 39104
Dermatologische Gemeinschaftspraxis Dres. Quist PartG
Mainz, Rhineland-Palatinate, 55128
Dermatologie Mölln, Praxis Dr Segert
Mölln, 23879
ZENTderma, Dr. Rolf Ostendorf
Mönchengladbach, 41061
Hautarztpraxis Dorittke / Kardorff
Mönchengladbach, 41236
Praxis Dr. Quack
München, 81539
Hautarztpraxis Dr. Susanne Gißler-Walter
Mutterstadt, 67112
Dermatologische Praxis im Hautzentrum Johannis Dr. med. Esther Völkel
Nuremberg, 90419
Hautarztpraxis Mortazawi
Remscheid, 42897
Dermatologische Spezialpraxis Dr. med. Ralph von Kiedrowski
Selters, 56242
Dermatologisches Studienzentrum Hunsrück - DSH
Simmern, 55469
Hautarztpraxis Dr. Hoffmann
Witten, 58453
About this study
Official title: This is a Prospective, Single-arm, Multicenter, Observational Non-interventional Study (NIS) in Germany of Patient Characteristics, Usage, and Effectiveness of Abrocitinib in Patients With Moderate to Severe Atopic Dermatitis (AD)
The purpose of this non-interventional observational study is to learn about the safety and effects of the medicinal product (called Abrocitinib) for the potential treatment of moderate to severe atopic dermatitis (AD). AD is a long-lasting disease that causes redness and irritation of the skin. This non-interventional study is seeking participants who is eligible for Abrocitinib treatment according to the summary of product characteristics (SmPC):
- Are aged at least 18 years old
- Have a confirmed diagnosis of AD by a skin doctor
- Decide to start treatment with Abrocitinib as part of routine clinical practice
- Have a personally signed and dated informed consent document. This is used to indicate that the patient has been informed of all pertinent aspects of the study and data privacy aspects
Participants will take the medicinal product as prescribed in the real-world setting. We will examine the experiences of people receiving Abrocitinib. This will help us determine if the medicinal product is effective and safe. Participants will take part in this study for 3 months. During this time, participants will be followed up from the date of their first Abrocitinib prescription for 12 months. During this non-interventional study, some participants may switch to other therapies after their initial Abrocitinib therapy. We will follow these participants further when they switch therapy to monitor their experiences. Participant documentation is expected quarterly as per standard clinical practice.
- Conditions
- Dermatitis, Atopic
- Keywords
- Atopic Dermatitis, Abrocitinib, JAK inhibitors
- Medical subject headings
- Dermatitis, Atopic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Evaluate the effectiveness, usage and patient characteristics of real-world use of Abrocitinib | This is a 60-month, prospective, non-interventional, multicenter study to evaluate the effectiveness, usage and patient characteristics of abrocitinib in patients with moderate to severe AD in a real-world setting. Eligible patients will be followed up from the date of first Abrocitinib prescription for 12 months. from the date of enrollment. Patients who are switched from the initial abrocitinib therapy to other therapies continue to be observed. Patient documentation is expected quarterly as per standard clinical practice. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants Who Achieved Investigator's Global Assessment (IGA) Score of Clear (0) or Almost Clear (1) at Month 3
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD. Percentage of participants with score of "Clear" (score 0) or "Almost Clear" (score 1) according to IGA were reported in this outcome measure.
Measured: At Month 3
Percentage of Participants With 75% Reduction From Baseline in Eczema Area and Severity Index (EASI) at Month 3
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of body surface area [BSA] affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD. EASI 75 response was defined as at least a 75% reduction in EASI relative to baseline.
Measured: At Month 3
Secondary outcomes (21)
Percentage of Participants Who Achieved IGA Score of Clear (0) or Almost Clear (1) Until End of Study
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that typically ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD. Percentage of participants with score of "Clear" (score 0) or "Almost Clear" (score 1) according to IGA were reported in this outcome measure.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With 75% Reduction From Baseline in EASI Score Until End of Study
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of BSA affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD. EASI 75 response was defined as at least a 75% reduction in EASI relative to baseline.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With 90% Reduction From Baseline in EASI Score Until End of Study
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of BSA affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD. EASI 90 response was defined as at least a 90% reduction in EASI relative to baseline.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants Who Achieved IGA Score of Clear (0) or Almost Clear (1) and a Reduction of >= 2 Points From Baseline Until End of Study
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that typically ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD. Percentage of participants with score of "Clear" (score 0) or "Almost Clear" (score 1) and a reduction of >=2 points from baseline according to IGA were reported in this outcome measure.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage Change From Baseline in IGA Total Score at Months 1, 3, 6, 9 and 12
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that typically ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Total Score at Months 1, 3, 6, 9 and 12
SCORAD total score was a validated scoring index for AD that assessed severity by combining A: extent, B: severity and C: subjective symptoms. A: a rule of 9 was used to calculate BSA affected by AD as a % of whole-BSA for each body region- head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; 1% for genitals. Score for each body region was added to determine A (0-100). B: severity of each sign (erythema; edema; oozing; excoriation; lichenification; dryness) was assessed as none =0, mild =1, moderate =2, severe =3, severity scores were added to give B (0-18). C: based on itching and sleep deprivation, each scored (0-10) where, 0= no itch/no sleeplessness and 10= worst imaginable itch/sleeplessness, scores for itch and sleeplessness were added to give C (0-20). The total score for an individual was calculated as A/5 + 7B/2 + C and ranged from 0-103; higher SCORAD scores = greater severity of AD.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Absolute EASI Total Score at Months 1, 3, 6, 9 and 12
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of BSA affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD.
Measured: At Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in EASI Total Score at Months 1, 3, 6, 9 and 12
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of BSA affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Absolute Change From Baseline in IGA Total Score at Months 1, 3, 6, 9 and 12
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that typically ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage of Participants Who Achieved at Least 4 Point Improvement on Pruritus Numerical Rating Scale (NRS) From Baseline Until End of Study
The pruritus-NRS comprised of one item and the score ranged from 0 ("no itch") to 10 ("worst imaginable itch"). Higher scores indicated greater severity. Participants were asked to rate the intensity of their average pruritus using this scale. Percentage of participants who achieved at least 4-point improvement on pruritus NRS are reported in this outcome measure.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With Pruritus NRS Score Less Than or Equal to (<=1)
The pruritus-NRS was comprised of one item and the score ranged from 0 ("no itch") to 10 ("worst imaginable itch"). Higher scores indicated greater severity. Participants were asked to rate the intensity of their average pruritus using this scale. Percentage of participants with pruritus NRS score <=1 are reported in this outcome measure.
Measured: From Baseline (Day 1) up to end of study (Month 12)
Percentage Change From Baseline in Peak-Pruritus (PP) NRS at Months 1, 3, 6, 9 and 12
PP NRS evaluated itching in the last 24 hours on a scale ranging from no itching (0) to worst possible itching (10). Higher scores indicated greater severity.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Patient Oriented Eczema Measure (POEM) Score at Months 1, 3, 6, 9 and 12
POEM was a participant-reported measure that assessed AD symptoms. The participants self-evaluated the frequency of occurrence and severity of 7 symptoms (such as itching and burning of the skin) within the last week, each according to a 5-point Likert scale from 0 ("at no day") to 4 ("at all days"). The total POEM score was summed over the symptoms and ranged from 0 (clear) to 28 points (very severe), where higher score indicated greater severity.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Medical Outcomes Study Sleep (MOS) Scale at Months 1, 3, 6, 9 and 12
The MOS-Sleep Scale is a self-administered questionnaire consisting of 12 items that assess key constructs of sleep. Instrument scoring yields 7 subscales (sleep disturbance, snoring, Sleep short of breath and headache, sleep quantity (raw scores), optimal sleep, sleep adequacy, and sleep somnolence) as well as sleep problems index I and II and all have score ranges from 0 (no sleep problems) to 100 (greater sleep problems), where higher scores indicated more sleep problems, with exception of sleep adequacy which was scored as 0 (least sleep adequacy) to 100 (better sleep adequacy) where higher scores indicated higher sleep adequacy, and optimal sleep scored as 0 (less quantity of sleep) to 24 (greater quantity of sleep), where higher scores indicated higher quantity sleep.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Dermatology Life Quality-Index (DLQI) Score at Months 1, 3, 6, 9 and 12
The DLQI was a 10-item participant-reported measure that rated how much a participant's skin problems had affected their life over the last week assigned to the following 6 dimensions: symptoms, daily life, leisure/sport, work/school, social life/relationship and treatment. Each question was scored from 0 to 3 where, 0=best quality of life and 3=greatest possible impairment of the quality of life (QoL). The total score was calculated as sum of scores and ranged from 0 (best QoL) to 30 (worst QoL), with higher scores indicating greater impairment of quality of life.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Hospital Anxiety and Depression Scale (HADS) Score at Months 1, 3, 6, 9 and 12
HADS was a validated 14-item questionnaire to assess states of anxiety and depression. HADS consisted of 2 subscales: HADS-Anxiety (HADS-A) scale and HADS-Depression (HADS-D) scale, each of which comprised of 7 items among adults who were physically ill. Each item was rated on a 4-point scale, with scores ranging from 0 to 3, with 0 denoting lowest and 3 denoting highest anxiety or depression level. For both subscales the total score was derived by summing up the respective 7 items with total score ranging from 0 (no presence of anxiety and depression) to 21 (severe feeling of anxiety and depression); higher score indicated greater severity of anxiety and depression.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in EuroQol Five-dimensional-five Level (EQ-5D-5L) Score at Months 1, 3, 6, 9 and 12
EQ-5D-5L was an instrument for measuring quality of life, including health benefits and health status on a visual analogue scale (VAS). EQ-5D health state profile has 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 levels: 1= no problems, 2= slight problems, 3= moderate problems, 4= severe problems, and 5= extreme problems. Responses to 5 dimensions comprise a health state/a single utility index value. E.g. if a participant responds "no problems" for each 5 dimensions, then health state was coded as "11111" with a predefined index value to it. Every health state (coded as combination of responses on each of 5 dimensions) has a unique predefined utility index value assigned to it, by EuroQol. Higher (positive) scores = better health state. The VAS component rates current health state on scale from 0 (worst imaginable health state) to 100 (best imaginable health state) ; higher scores indicate a better health state.
Measured: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Treatment Satisfaction Measured by Patient Benefit Index (PBI) at Months 1, 3, 6, 9 and 12
PBI consisted of two one-sided questionnaires which were completed by participants before and after receiving a treatment. Total of 23 possible treatment goals were evaluated on importance scale from 0 ("not at all") to 4 ("very"). "Does not apply to me" was coded as "0". PBI was calculated by multiplying achieved benefits (respective PBI after baseline) with importance of the respective needs prior to therapy (PBI at baseline), dividing these products by sum of all importance items (PBI at baseline) and summing them up for all items. Total PBI score ranged from 0 (no benefit) to 4 (maximal benefit), where higher scores indicated more benefits. PBI questionnaire measured satisfaction at all points in time after baseline.
Measured: At Months 1, 3, 6, 9 and 12
Number of Participants With Treatment Expectation Measured by PBI at Baseline
PBI consisted of two one-sided questionnaires which were completed by participants before and after receiving treatment. Total of 25 possible treatment goals were evaluated on importance scale from 0 (" not at all") to 4 ("very"), where higher scores indicated more important goals. The responses to each treatment goal included: somewhat, moderately, quite, very, does not apply to me, not answered and not at all. Treatment expectation was measured at baseline.
Measured: At Baseline (Day 1)
Number of Days With Topical Treatment Use
Topical treatments included topical corticosteroids and topical calcineurin inhibitors. Number of days with topical treatment use was reported in this outcome measure. Number of days was calculated as date of first topical treatment - date of last topical treatment + 1.
Measured: Months 1, 3, 6, 9 and 12
Number of Days of Emollients Use
Number of days with emollients use was calculated as: date of first emollients use - date of last emollients use + 1. The number of days with emollients use was reported in this outcome measure.
Measured: Months 1, 3, 6, 9 and 12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Feb 2022
- Study start10 May 2022
- Primary completion25 Jul 2024
- Study completion25 Jul 2024
Why it stopped: Business decision: Due to the slow recruitment, the sponsor decided to discontinue the study early.
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.
- Other trials for Dermatitis, AtopicStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 112 participants (actual)
- Target duration
- 12 Months
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
- NCT05250115
- Sponsor's protocol ID
- B7451089
- Other IDs
- ABROAD
- Status last verified
- Sep 2025
- First submitted
- 10 Feb 2022
- Last updated
- 29 Sep 2025
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- Individual data sharing
- No: 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.
Study at a glance
From the registry record, last updated by the sponsor on 29 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- This is a Prospective, Single-arm, Multicenter, Observational Non-interventional Study (NIS) in Germany of Patient Characteristics, Usage, and Effectiveness of Abrocitinib in Patients With Moderate to Severe Atopic Dermatitis (AD)
- ClinicalTrials.gov ID
- NCT05250115
- Acronym / sponsor ID
- B7451089
- Conditions
- Dermatitis, Atopic
- Keywords
- Atopic Dermatitis, Abrocitinib, JAK inhibitors
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Business decision: Due to the slow recruitment, the sponsor decided to discontinue the study early.
- Enrolment
- 112 participants (actual)
- Lead sponsor
- PfizerIndustry (pharma, biotech, devices)
- Study start
- 10 May 2022 (actual)
- Primary completion
- 25 Jul 2024 (actual)
- Study completion
- 25 Jul 2024 (actual)
- First posted
- 22 Feb 2022 (actual)
- Results
- Posted 29 Sep 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this non-interventional observational study is to learn about the safety and effects of the medicinal product (called Abrocitinib) for the potential treatment of moderate to severe atopic dermatitis (AD). AD is a long-lasting disease that causes redness and irritation of the skin. This non-interventional study is seeking participants who is eligible for Abrocitinib treatment according to the summary of product characteristics (SmPC):
- Are aged at least 18 years old
- Have a confirmed diagnosis of AD by a skin doctor
- Decide to start treatment with Abrocitinib as part of routine clinical practice
- Have a personally signed and dated informed consent document. This is used to indicate that the patient has been informed of all pertinent aspects of the study and data privacy aspects
Participants will take the medicinal product as prescribed in the real-world setting. We will examine the experiences of people receiving Abrocitinib. This will help us determine if the medicinal product is effective and safe. Participants will take part in this study for 3 months. During this time, participants will be followed up from the date of their first Abrocitinib prescription for 12 months. During this non-interventional study, some participants may switch to other therapies after their initial Abrocitinib therapy. We will follow these participants further when they switch therapy to monitor their experiences. Participant documentation is expected quarterly as per standard clinical practice.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 12 Months
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Evaluate the effectiveness, usage and patient characteristics of real-world use of Abrocitinib | – | –This is a 60-month, prospective, non-interventional, multicenter study to evaluate the effectiveness, usage and patient characteristics of abrocitinib in patients with moderate to severe AD in a real-world setting. Eligible patients will be followed up from the date of first Abrocitinib prescription for 12 months. from the date of enrollment. Patients who are switched from the initial abrocitinib therapy to other therapies continue to be observed. Patient documentation is expected quarterly as per standard clinical practice. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- A prospective, single-arm, multi-center, observational non-interventional study looking at adult patients with moderate-severe atopic dermatitis, who have been chosen to start treatment with Abrocitinib in Germany according to the current routine practice of the treating physician.
Key inclusion criteria (7 listed)
- Patients aged ≥18 years
- Confirmed diagnosis of AD by dermatologist prior to study inclusion
- Patient for whom the decision to initiate treatment with abrocitinib was made as part of routine clinical practice irrespective of the patients being
- Patient is eligible for abrocitinib treatment according to Summary of Product Characteristics (SmPC)
- Evidence of a personally signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the non-interventional study
Key exclusion criteria (5 listed)
- Contraindications according to SmPC
- Receipt of any investigational drug within 3 months or longer if required according to wash-out period prior to inclusion or participation in a clinical trial during observation period
- Patients being treated with abrocitinib within a time period of <28 days prior to the timepoint of study inclusion
- Patients who are investigational site staff members or patients who are Pfizer employees directly involved in the conduct of the non-interventional study
- Patients who are unable to consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Percentage of Participants Who Achieved Investigator's Global Assessment (IGA) Score of Clear (0) or Almost Clear (1) at Month 3
Time frame: At Month 3
The IGA is a tool used to assess the severity of AD (excluding scalp, palms and soles) on a 5-point scale that ranges from 0 to 4, where 0 indicates clear (no signs of AD), 1 indicates almost clear (minimal signs of AD), 2 indicates mild AD, 3 indicates moderate AD and 4 indicates severe AD, higher scores indicated greater severity of AD. Percentage of participants with score of "Clear" (score 0) or "Almost Clear" (score 1) according to IGA were reported in this outcome measure.
Percentage of Participants With 75% Reduction From Baseline in Eczema Area and Severity Index (EASI) at Month 3
Time frame: At Month 3
The EASI assessed both clinical signs of AD as well as extent of disease. For body regions such as "head and neck", "trunk", "upper extremities" and "lower extremities" the extent of eczema was assessed by an area score between 0 (0% of body surface area [BSA] affected) and 6 (90 to 100% of BSA affected), respectively. For each area the severity of clinical signs of AD such as "erythema", "edema/papulation", "excoriation" and "lichenification" were scored from 0 to 3, respectively where 0= absent; 1= mild; 2= moderate; 3= severe. The scores for the signs were added for each area and multiplied by the respective area score. The EASI for an individual was calculated as weighted sum: 0.1*score for head/neck + 0.3*score for trunk + 0.2*score for upper extremities + 0.4*score for lower extremities. The total score ranged from 0 to 72, higher scores represented greater severity of AD. EASI 75 response was defined as at least a 75% reduction in EASI relative to baseline.
21 secondary outcomes
Percentage of Participants Who Achieved IGA Score of Clear (0) or Almost Clear (1) Until End of Study
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With 75% Reduction From Baseline in EASI Score Until End of Study
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With 90% Reduction From Baseline in EASI Score Until End of Study
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants Who Achieved IGA Score of Clear (0) or Almost Clear (1) and a Reduction of >= 2 Points From Baseline Until End of Study
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage Change From Baseline in IGA Total Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Scoring Atopic Dermatitis (SCORAD) Total Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Absolute EASI Total Score at Months 1, 3, 6, 9 and 12
Time frame: At Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in EASI Total Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Absolute Change From Baseline in IGA Total Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage of Participants Who Achieved at Least 4 Point Improvement on Pruritus Numerical Rating Scale (NRS) From Baseline Until End of Study
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage of Participants With Pruritus NRS Score Less Than or Equal to (<=1)
Time frame: From Baseline (Day 1) up to end of study (Month 12)
Percentage Change From Baseline in Peak-Pruritus (PP) NRS at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Patient Oriented Eczema Measure (POEM) Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Medical Outcomes Study Sleep (MOS) Scale at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Dermatology Life Quality-Index (DLQI) Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in Hospital Anxiety and Depression Scale (HADS) Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Percentage Change From Baseline in EuroQol Five-dimensional-five Level (EQ-5D-5L) Score at Months 1, 3, 6, 9 and 12
Time frame: Baseline (Day 1), Months 1, 3, 6, 9 and 12
Treatment Satisfaction Measured by Patient Benefit Index (PBI) at Months 1, 3, 6, 9 and 12
Time frame: At Months 1, 3, 6, 9 and 12
Number of Participants With Treatment Expectation Measured by PBI at Baseline
Time frame: At Baseline (Day 1)
Number of Days With Topical Treatment Use
Time frame: Months 1, 3, 6, 9 and 12
Number of Days of Emollients Use
Time frame: Months 1, 3, 6, 9 and 12
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Sep 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- To obtain contact information for a study center near you, click here.Link provided by the sponsor.
- Individual participant dataSharing planned: No. 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
38 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Dermatitis, Atopic, run by Pfizer at 38 sites in Germany.
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 7 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: stopped early, as of the sponsor's last update on 29 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 38 sites in Germany. 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. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Yes. Results are posted in the registry (first posted 29 Sep 2025). 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 Who Achieved Investigator's Global Assessment (IGA) Score of Clear (0) or Almost Clear (1) at Month 3 (time frame: At Month 3). 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?
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 29 Sep 2025; AzTrials last refreshed its copy on 7 Nov 2026.