Rheumatoid ArthritisPhase 2NCT00938587
A Study Of PF-04171327 In The Treatment Of The Signs And Symptoms Of Rheumatoid Arthritis
A Phase 2 study testing PF-04171327 10 mg, PF-04171327 25 mg and Prednisone 5 mg in people with Rheumatoid Arthritis, run by Pfizer at 41 sites in 13 countries.
Trial summary
This study will investigate the safety and efficacy of an investigational drug, PF-04171327 on the signs and symptoms of rheumatoid arthritis in patients that require glucocorticoids while on background methotrexate. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Rheumatoid Arthritis
- What is being tested?
- PF-04171327 10 mg, PF-04171327 25 mg and Prednisone 5 mg
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 86 participants
- Where
- 41 sitesin 13 countries
- Study dates
- 7 Oct 2009to 29 Jul 2010
- Phase
- Phase 2
- 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
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients ≥ 18 years of age, diagnosed with rheumatoid arthritis for a minimum duration of 3 months
- On stable dose of methotrexate for at least 6 weeks prior to screening
- Patient must have minimum disease activity level of ≥ 6 tender/painful joints, ≥ 6 swollen joints and CRP ≥ 0.7 mg/dL
- Not currently receiving steroid medication
Who cannot join
- Pregnant or nursing women
- Patients that have active infections, TB, HIV and/or Hepatitis B or C
- Patients that have a history of intolerance or significant adverse effects with the use of glucocorticoids
Trial locations and contacts
41 sites in 13 countries.
41 sites in 13 countries
United States10 sites
Anniston Medical Clinic, PC
Anniston, Alabama, 36207
Pinnacle Research Group, LLC
Anniston, Alabama, 36207
Premier Imaging Center
Bingham Farms, Michigan, 48025
Quest Research Institute
Bingham Farms, Michigan, 48025
Allergy, Asthma, Arthritis and Lung
Daytona Beach, Florida, 32114
Altoona Center for Clinical Research
Duncansville, Pennsylvania, 16635
Elite Research Institute
Miami, Florida, 33169
Millennium Research
Ormond Beach, Florida, 32174
The Arthritis Center
Springfield, Illinois, 62704
Florida Medical Clinic, PA
Zephyrhills, Florida, 33542
Czechia5 sites
MEDIPONT Plus, s.r.o.
České Budějovice, 370 01
ARTMEDI UPD s r.o.
Hostivice, 253 01
Revmatologicka ambulance
Prague, 140 00
Fakultni Thomayerova nemocnice s poliklinikou
Prague, 140 59
DC Mediscan
Praha 11 - Chodov, 148 00
Ukraine5 sites
Chair of Cardiology & Functional Diagnostic
Kharkiv, 61176
State Institution "Institute of Gerontology of AMS of Ukraine"
Kyiv, 04114
State Institution 'Institute of Gerontology of AMS of Ukraine'
Kyiv, 04114
Municipal City Clinical Hospital #4, Department of Rheumatology
Lviv, 79011
Vinnitsa Regional Clinical Hospital n.a. Pirogov
Vinnitsa, 21018
Hungary4 sites
Dr. Rethy Pal Korhaz es Rendelointezet\Reumatologia
Békéscsaba, 5600
Synexus Magyarorszag Kft.
Budapest, H-1036
Debreceni Egyetem Orvos és Egeszsegtudomanyi Centrum
Debrecen, 4032
MAV Korhaz es Rendelointezet
Szolnok, H-5000
Russia4 sites
Moscow SHI City Clinical Hospital #4, Department of Therapy of Moscow Faculty
Moscow, 115093
Institution of Russian Academy of Medical Sciences Research Institute of Rheumatology RAMS
Moscow, 115522
SI Saint-Petersburg SRI for Emergency Care named after I.I. Dzhanelidze
Saint Petersburg, 192242
Regional State Institution of Healthcare Smolensk Regional Clinical Hospital
Smolensk, 214018
Spain4 sites
Hospital de Cruces
Barakaldo, Bilbao, 48903
Hospital de Basurto
Bilbao, Vizcaya, 48013
Hospital Nuestra Señora de La Esperanza
Santiago de Compostela, A Coruña, 15705
Hospital Universitario Virgen Macarena
Seville, 41009
Serbia2 sites
Institute of Rheumatology
Belgrade, 11000
Institute for Rheumatic and Cardiovascular Disease Niska Banja
Niška Banja, 18205
Slovakia2 sites
Narodny ustav reumatickych chorob, Klinicke oddelenie
Piešťany, 921 12
Nestatna reumatologicka ambulancia, MUDr. Pavol Polak, s.r.o.
Žilina, 010 01
Hong Kong1 site
Centre for Assessment and Treatment of Rheumatic Diseases, Department of Medicine and Geriatrics
New Territories
South Korea1 site
Severance Hospital, Yonsei University College of Medicine, Rheumatology, Internal Medicine
Seoul, 120-752
Turkey (Türkiye)1 site
Ankara University School fo Medicine
Ankara, 06100
About this study
Official title: A PHASE 2A, RANDOMIZED, DOUBLE-BLIND, ACTIVE AND PLACEBO-CONTROLLED STUDY OF PF-04171327 IN THE TREATMENT OF THE SIGNS AND SYMPTOMS OF RHEUMATOID ARTHRITIS
This study will investigate the safety and efficacy of an investigational drug, PF-04171327 on the signs and symptoms of rheumatoid arthritis in patients that require glucocorticoids while on background methotrexate. This study will also look at the response of chemical and biological markers in rheumatoid arthritis patients. Lastly, this study will measure the PK (amount of drug in the blood) of methotrexate while patients may be taking PF-04171327.
- Conditions
- Rheumatoid Arthritis
- Being tested
- PF-04171327 10 mg, Prednisone Placebo, PF-04171327 25 mg, Prednisone 5 mg, Placebo for PF-04171327
- Keywords
- Rheumatoid Arthritis Glucocorticoids Prednisone
- Medical subject headings
- Arthritis, Rheumatoid
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PF-04171327 10 mgDrug
PF-04171327 10 mg tablet every day for 14 days
Prednisone PlaceboOther
Placebo for Prednisone 5 mg tablet every day for 14 days
PF-04171327 25 mgDrug
PF-04171327 25 mg tablet every day for 14 days
Prednisone PlaceboOther
Placebo for Prednisone 5 mg tablet every day for 14 days
Prednisone 5 mgDrug
Prednisone 5 mg tablet every day for 14 days
Placebo for PF-04171327Other
Placebo for PF-04171327 every day for 14 days
PlaceboOther
Placebo tablet every day for 14 days
Placebo for PF-04171327Other
Placebo tablet every day for 14 days
| Study group | Role | What they receive |
|---|---|---|
| PF-04171327 10 mg | Experimental | Not described Receives: Drug: PF-04171327 10 mg; Other: Prednisone Placebo |
| PF-04171327 25 mg | Experimental | Not described Receives: Drug: PF-04171327 25 mg; Other: Prednisone Placebo |
| Prednisone | Active comparator | Not described Receives: Drug: Prednisone 5 mg; Other: Placebo for PF-04171327 |
| Placebo | Placebo comparator | Not described Receives: Other: Placebo; Other: Placebo for PF-04171327 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (4 Variables) (DAS28-4 [CRP]) at Day 14
DAS28-4 (CRP) examines progression or improvement of RA. It was assessed from swollen joint count (SJC) and tender joint count (TJC) using the 28 joints count, CRP (normal range of CRP is less than (<) 10 milligram per liter [mg/L], decrease in the level of CRP indicates reduction in inflammation) and participant global assessment (PGA) of disease activity (participant global assessment of diseases condition scores ranging from 0 [very well condition] to 100 [very poor condition], higher scores indicated greater affectation due to disease activity). Total DAS28-4 (CRP) transformed score range: 0 (least severe) to 10 (most severe), higher scores indicate more severe disease activity. DAS28-4 (CRP) scores: less than equal to (<=) 3.2 implied low disease activity; greater than (>) 3.2 to 5.1 implied moderate to high disease activity.
Measured: Baseline, Day 14
Secondary outcomes (27)
Change From Baseline in Tender Joints Count at Day 7, 14, 42
Number of tender joints was determined by examining 28 joints and identified the joints that were painful under pressure or to passive motion. The number of tender joints was recorded on the joint assessment form at each visit, no tenderness = 0, tenderness = 1.
Measured: Baseline, Day 7, 14, 42
Change From Baseline in Swollen Joints Count at Day 7, 14 and 42
Number of swollen joints was determined by examination of 28 joints and identifying if swelling was present. The number of swollen joints was recorded on the joint assessment form at each visit, no swelling = 0, swelling =1.
Measured: Baseline, Day 7, 14, 42
Change From Baseline in C-Reactive Protein (CRP) at Day 7, 14 and 42
The test for CRP is a laboratory measurement for evaluation of an acute phase reactant of inflammation through the use of an ultrasensitive assay. Normal range of CRP is less than (<) 10 mg/L. A decrease in the level of CRP indicates reduction in inflammation and therefore improvement.
Measured: Baseline, Day 7, 14, 42
Change From Baseline in Health Assessment Questionnaire-Disability Index (HAQ-DI) Score at Day 7 and 14
HAQ-DI assessed the ability of participants to perform task in 8 domains of daily living activities: dress/groom, arise, eat, walk, reach, grip, hygiene, and common activities. Each item was scored on a 4-point scale ranging from 0 to 3: 0= no difficulty; 1= some difficulty; 2= much difficulty; 3= unable to do, higher scores indicate more difficulty. Overall score was computed as the sum of domain scores and divided by the number of domains answered. Total possible HAQ-DI score range: 0 (no difficulty) to 3 (extreme difficulty), where higher scores indicate more difficulty while performing daily living activities.
Measured: Baseline, Day 7, 14
Change From Baseline in Participant Assessment of Arthritis Pain at Day 7 and 14
Participant assessment of arthritis pain included assessment of severity of arthritis pain using a 100 millimeter (mm) visual analog scale (VAS). Participants placed a mark on the VAS between 0 mm (no pain) and 100 mm (most severe pain), which corresponded to the magnitude of their pain, higher scores indicate more pain.
Measured: Baseline, Day 7, 14
Change From Baseline in Participant Global Assessment (PGA) of Arthritis at Day 7 and 14
PGA was a questionnaire where participants answered the following question, "Considering all the ways your arthritis affects you, how are you feeling today?" The participants' response were recorded using a 100 mm visual analog scale placing a mark on the scale, between 0 mm (very well condition) to 100 mm (very poor condition). Higher scores indicate higher degree of arthritis.
Measured: Baseline, Day 7, 14
Change From Baseline in Physician Global Assessment (PhGA) of Arthritis at Day 7 and 14
PhGA included assessment of severity of arthritis pain where physicians were asked to rate the severity of the participant's overall arthritis. The physician's response was recorded using a visual analog scale between 0 mm (very good condition) to 100 mm (very poor condition). Higher scores indicate higher degree of arthritis.
Measured: Baseline, Day 7, 14
Change From Baseline in 36-Item Short-Form Health Survey (SF-36) Version 2.0 (V2) at Day 14
SF-36 is a standardized survey evaluating 8 aspects of functional health and well-being: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional and mental health. Score for each of the 8 aspects are scaled from 0 (worst condition) to 100 (best condition), where higher scores indicate better health status. These 8 domains were also reported as two summary scores: physical component scores and mental component scores. Score range for each of the 2 summary scores = 0 (worst condition) to 100 (best condition), where higher scores represent better health status.
Measured: Baseline, Day 14 (D14)
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (3 Variables) (DAS28-3 [CRP]) at Day 7, 14 and 42
DAS28-3 (CRP) was calculated from the swollen joint count and tender joint count using the 28 joints count and CRP (normal range of CRP is <10 mg/L, decrease in the level of CRP indicates reduction in inflammation). Total DAS28-3 (CRP) score range: 0 (least severe) to 9.4 (most severe), higher scores indicate more disease activity.
Measured: Baseline, Day 7, 14, 42
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (4 Variables) (DAS28-4 [CRP]) at Day 7
DAS28-4 (CRP) examines progression or improvement of RA. It was assessed from SJC and TJC using the 28 joints count, CRP (normal range of CRP is <10 mg/L, decrease in the level of CRP indicates reduction in inflammation) and PGA of disease activity (participant global assessment of diseases condition scores ranging from 0 [very well condition] to 100 [very poor condition], higher scores indicated greater affectation due to disease activity). Total DAS28-4 (CRP) transformed score range: 0 (least severe) to 10 (most severe), higher scores indicate more severe disease activity. DAS28-4 (CRP) scores: <=3.2 implied low disease activity; >3.2 to 5.1 implied moderate to high disease activity.
Measured: Baseline, Day 7
Percentage of Participants Achieving American College of Rheumatology 20% (ACR20) Response at Day 7 and 14
ACR20 responder: participants who achieved at =20% improvement in tender and swollen 28-joints count, and >=20% improvement in at least 3 of the following 5 measures: 1) participant's assessment of arthritis pain (participant's self-assessed severity of arthritis pain, score range from 0[no pain] to 100[most severe pain], higher scores=more pain), 2) PGA of arthritis (participant's assessed overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 3) PhGA of arthritis (physician rated severity of participants overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 4) HAQ-DI (assessment of functional disability, score range from 0[no difficulty] to 3[extreme difficulty], higher scores=more functional limitation) and 5) CRP (assessment of inflammation, normal range of CRP is <10 mg/L, decrease in the level of CRP=reduction in inflammation).
Measured: Day 7, 14
Percentage of Participants Achieving American College of Rheumatology 50% (ACR50) Response at Day 7 and 14
ACR50 responder: participants who achieved at =50% improvement in tender and swollen 28-joints count, and >=50% improvement in at least 3 of the following 5 measures: 1) participant's assessment of arthritis pain (participant's self-assessed severity of arthritis pain, score range from 0[no pain] to 100[most severe pain], higher scores=more pain), 2) PGA of arthritis (participant's assessed overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 3) PhGA of arthritis (physician rated severity of participants overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 4) HAQ-DI (assessment of functional disability, score range from 0[no difficulty] to 3[extreme difficulty], higher scores=more functional limitation) and 5) CRP (assessment of inflammation, normal range of CRP is <10 mg/L, decrease in the level of CRP=reduction in inflammation).
Measured: Day 7, 14
Percentage of Participants Achieving American College of Rheumatology 70% (ACR70) Response at Day 7 and 14
ACR70 responder: participants who achieved at =70% improvement in tender and swollen 28-joints count, and >=70% improvement in at least 3 of the following 5 measures: 1) participant's assessment of arthritis pain (participant's self-assessed severity of arthritis pain, score range from 0[no pain] to 100[most severe pain], higher scores=more pain), 2) PGA of arthritis (participant's assessed overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 3) PhGA of arthritis (physician rated severity of participants overall arthritis activity, score range from 0[no arthritis] to 100[extreme arthritis], higher scores=higher degree of arthritis), 4) HAQ-DI (assessment of functional disability, score range from 0[no difficulty] to 3[extreme difficulty], higher scores=more functional limitation) and 5) CRP (assessment of inflammation, normal range of CRP is <10 mg/L, decrease in the level of CRP=reduction in inflammation).
Measured: Day 7, 14
Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)
An AE was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent are events between first dose of study drug and up to 31 days after last dose (Day 45) that were absent before treatment or that worsened relative to pretreatment state.
Measured: Baseline up to Day 45
Number of Participants With Clinically Significant Change From Baseline in Laboratory Abnormalities
Criteria for laboratory abnormalities: Hematology (hemoglobin, hematocrit <0.8*baseline; platelet count <75 or >700*10^3 per mm^3; leucocytes <2.5 or >17.5*10^3 per mm^3); chemistry (total bilirubin >1.5*upper limit of reference range [ULN]; aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transpeptidase, alkaline phosphatase, >3.0*ULN; total protein, albumin <0.8*lower limit of reference range [LLN] or >1.2*ULN; blood urea nitrogen [BUN]/urea, creatinine >1.3*ULN; glucose [fasting] <0.6*LLN or >1.5*ULN; uric acid >1.2*ULN; sodium <0.95*LLN or >1.05*ULN; potassium, calcium <0.9*LLN or >1.1*ULN; albumin, total protein <0.8*LLN or >1.2*ULN; urinalysis (urine white blood cell (WBC) =>6/ high power field (hpf); urine red blood cell (RBC) =>6/hpf). Number of participants with clinically significant change from baseline in laboratory abnormalities identified by investigator were reported.
Measured: Baseline up to Day 45
Change From Baseline in Body Weight at Day 7 and 14
Measured: Baseline, Day 7, 14
Number of Participants With Clinically Significant Vital Signs Abnormalities
Following parameters were analyzed for examination of vital signs: systolic and diastolic blood pressure, heart rate and body temperature. Vital sign measurements were performed with the participant in the seated position. Clinical significance vital sign abnormality was determined by investigator.
Measured: Baseline up to Day 45
Number of Participants With Clinically Significant Electrocardiogram (ECG) Abnormalities
Clinically significant ECG findings included PR interval >=300 milliseconds (msec) or >=25% increase from baseline (if baseline PR interval >200 msec) or >=50% increase (if baseline PR interval less than or equal to [<=] 200 msec); QRS interval >=200 msec or >=25% increase from baseline (if baseline PR interval >100 msec) or >=50% increase (if baseline PR interval <= 100 msec); QT interval >=500 msec, corrected QT interval >=500 msec.
Measured: Baseline up to Day 45
Plasma Concentration of PF-00251802 Versus Time Summary on Day 7 and Day 14
Plasma concentration of PF-00251802 versus time summary, a metabolite of PF-04171327 was reported in this outcome measure.
Measured: 0, 1, 2, 3 and 4 hours post-dose on Day 7, 14
Ratio of Apparent Oral Clearance on Day 1 to Day 14 of Methotrexate
Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood. Methotrexate was used as a background therapy by participants.
Measured: Pre-dose (0 hour), 1, 2, 3 and 4 hours post-dose
Change From Baseline in Lymphocyte Counts at Day 1, 7 and 14
Measured: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Neutrophil Counts at Day 1, 7 and 14
Measured: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Eosinophil Counts at Day 1, 7 and 14
Measured: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Osteocalcin Level at Day 1, 7 and 14
Measured: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Plasma Cortisol Level at Day 1, 7 and 14
Measured: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Ratio of Urinary N-terminal Telopeptide of Type 1 Collagen (uNTX-I) Level to Urinary Creatinine (uCr) Level at Day 7 and 14
Unit of ratio of urinary N-terminal telopeptide of type 1 collagen (uNTX-I) level to urinary creatinine (uCr) level was nanomoles bone collagen equivalents (nmol bce) per millimole creatinine (mmol cr).
Measured: Baseline, Day 7 and 14
Change From Baseline in Adiponectin Level at Day 7 and 14
Measured: Baseline, Day 7 and 14
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jul 2009 (estimated)
- Study start7 Oct 2009
- Primary completion29 Jul 2010
- Study completion29 Jul 2010
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 Rheumatoid ArthritisStudies 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 86 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
- NCT00938587
- Sponsor's protocol ID
- A9391005
- Other IDs
- 2009-013223-37, 2009
- Status last verified
- Nov 2023
- First submitted
- 13 Jul 2009
- Last updated
- 22 Nov 2023
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- 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.
Study at a glance
From the registry record, last updated by the sponsor on 22 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A PHASE 2A, RANDOMIZED, DOUBLE-BLIND, ACTIVE AND PLACEBO-CONTROLLED STUDY OF PF-04171327 IN THE TREATMENT OF THE SIGNS AND SYMPTOMS OF RHEUMATOID ARTHRITIS
- ClinicalTrials.gov ID
- NCT00938587
- Acronym / sponsor ID
- A9391005
- Conditions
- Rheumatoid Arthritis
- Keywords
- Rheumatoid Arthritis Glucocorticoids Prednisone
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 86 participants (actual)
- Lead sponsor
- PfizerIndustry (pharma, biotech, devices)
- Study start
- 7 Oct 2009 (actual)
- Primary completion
- 29 Jul 2010 (actual)
- Study completion
- 29 Jul 2010 (actual)
- First posted
- 14 Jul 2009 (estimated)
- Results
- Posted 22 Nov 2023
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will investigate the safety and efficacy of an investigational drug, PF-04171327 on the signs and symptoms of rheumatoid arthritis in patients that require glucocorticoids while on background methotrexate. This study will also look at the response of chemical and biological markers in rheumatoid arthritis patients. Lastly, this study will measure the PK (amount of drug in the blood) of methotrexate while patients may be taking PF-04171327.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| PF-04171327 10 mg | Experimental | Drug: PF-04171327 10 mg, Other: Prednisone Placebo |
| PF-04171327 25 mg | Experimental | Drug: PF-04171327 25 mg, Other: Prednisone Placebo |
| Prednisone | Active comparator | Drug: Prednisone 5 mg, Other: Placebo for PF-04171327 |
| Placebo | Placebo comparator | Other: Placebo, Other: Placebo for PF-04171327 |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Patients ≥ 18 years of age, diagnosed with rheumatoid arthritis for a minimum duration of 3 months
- On stable dose of methotrexate for at least 6 weeks prior to screening
- Patient must have minimum disease activity level of ≥ 6 tender/painful joints, ≥ 6 swollen joints and CRP ≥ 0.7 mg/dL
- Not currently receiving steroid medication
Key exclusion criteria (3 listed)
- Pregnant or nursing women
- Patients that have active infections, TB, HIV and/or Hepatitis B or C
- Patients that have a history of intolerance or significant adverse effects with the use of glucocorticoids
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-04171327 10 mgPF-04171327 10 mg tablet every day for 14 days | Drug | PF-04171327 10 mg |
| Prednisone PlaceboPlacebo for Prednisone 5 mg tablet every day for 14 days | Other | PF-04171327 10 mg |
| PF-04171327 25 mgPF-04171327 25 mg tablet every day for 14 days | Drug | PF-04171327 25 mg |
| Prednisone PlaceboPlacebo for Prednisone 5 mg tablet every day for 14 days | Other | PF-04171327 25 mg |
| Prednisone 5 mgPrednisone 5 mg tablet every day for 14 days | Drug | Prednisone |
| Placebo for PF-04171327Placebo for PF-04171327 every day for 14 days | Other | Prednisone |
| PlaceboPlacebo tablet every day for 14 days | Other | Placebo |
| Placebo for PF-04171327Placebo tablet every day for 14 days | Other | Placebo |
Primary outcome
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (4 Variables) (DAS28-4 [CRP]) at Day 14
Time frame: Baseline, Day 14
DAS28-4 (CRP) examines progression or improvement of RA. It was assessed from swollen joint count (SJC) and tender joint count (TJC) using the 28 joints count, CRP (normal range of CRP is less than (<) 10 milligram per liter [mg/L], decrease in the level of CRP indicates reduction in inflammation) and participant global assessment (PGA) of disease activity (participant global assessment of diseases condition scores ranging from 0 [very well condition] to 100 [very poor condition], higher scores indicated greater affectation due to disease activity). Total DAS28-4 (CRP) transformed score range: 0 (least severe) to 10 (most severe), higher scores indicate more severe disease activity. DAS28-4 (CRP) scores: less than equal to (<=) 3.2 implied low disease activity; greater than (>) 3.2 to 5.1 implied moderate to high disease activity.
27 secondary outcomes
Change From Baseline in Tender Joints Count at Day 7, 14, 42
Time frame: Baseline, Day 7, 14, 42
Change From Baseline in Swollen Joints Count at Day 7, 14 and 42
Time frame: Baseline, Day 7, 14, 42
Change From Baseline in C-Reactive Protein (CRP) at Day 7, 14 and 42
Time frame: Baseline, Day 7, 14, 42
Change From Baseline in Health Assessment Questionnaire-Disability Index (HAQ-DI) Score at Day 7 and 14
Time frame: Baseline, Day 7, 14
Change From Baseline in Participant Assessment of Arthritis Pain at Day 7 and 14
Time frame: Baseline, Day 7, 14
Change From Baseline in Participant Global Assessment (PGA) of Arthritis at Day 7 and 14
Time frame: Baseline, Day 7, 14
Change From Baseline in Physician Global Assessment (PhGA) of Arthritis at Day 7 and 14
Time frame: Baseline, Day 7, 14
Change From Baseline in 36-Item Short-Form Health Survey (SF-36) Version 2.0 (V2) at Day 14
Time frame: Baseline, Day 14 (D14)
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (3 Variables) (DAS28-3 [CRP]) at Day 7, 14 and 42
Time frame: Baseline, Day 7, 14, 42
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (4 Variables) (DAS28-4 [CRP]) at Day 7
Time frame: Baseline, Day 7
Percentage of Participants Achieving American College of Rheumatology 20% (ACR20) Response at Day 7 and 14
Time frame: Day 7, 14
Percentage of Participants Achieving American College of Rheumatology 50% (ACR50) Response at Day 7 and 14
Time frame: Day 7, 14
Percentage of Participants Achieving American College of Rheumatology 70% (ACR70) Response at Day 7 and 14
Time frame: Day 7, 14
Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time frame: Baseline up to Day 45
Number of Participants With Clinically Significant Change From Baseline in Laboratory Abnormalities
Time frame: Baseline up to Day 45
Change From Baseline in Body Weight at Day 7 and 14
Time frame: Baseline, Day 7, 14
Number of Participants With Clinically Significant Vital Signs Abnormalities
Time frame: Baseline up to Day 45
Number of Participants With Clinically Significant Electrocardiogram (ECG) Abnormalities
Time frame: Baseline up to Day 45
Plasma Concentration of PF-00251802 Versus Time Summary on Day 7 and Day 14
Time frame: 0, 1, 2, 3 and 4 hours post-dose on Day 7, 14
Ratio of Apparent Oral Clearance on Day 1 to Day 14 of Methotrexate
Time frame: Pre-dose (0 hour), 1, 2, 3 and 4 hours post-dose
Change From Baseline in Lymphocyte Counts at Day 1, 7 and 14
Time frame: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Neutrophil Counts at Day 1, 7 and 14
Time frame: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Eosinophil Counts at Day 1, 7 and 14
Time frame: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Osteocalcin Level at Day 1, 7 and 14
Time frame: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Plasma Cortisol Level at Day 1, 7 and 14
Time frame: Baseline; 1, 2, 3 and 4 hours post-dose on Day 1; 0, 1, 2, 3 and 4 hours post-dose on Day 7 and 14
Change From Baseline in Ratio of Urinary N-terminal Telopeptide of Type 1 Collagen (uNTX-I) Level to Urinary Creatinine (uCr) Level at Day 7 and 14
Time frame: Baseline, Day 7 and 14
Change From Baseline in Adiponectin Level at Day 7 and 14
Time frame: Baseline, Day 7 and 14
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Nov 2023.
- 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: 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
41 sites in 13 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing PF-04171327 10 mg, PF-04171327 25 mg and Prednisone 5 mg in people with Rheumatoid Arthritis, run by Pfizer at 41 sites in 13 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 4 inclusion and 3 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 22 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 41 sites in United States, Czechia, Ukraine, Hungary, Russia and 8 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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 22 Nov 2023). 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?
Change From Baseline in Disease Activity Score Based on 28-Joints Count and C-Reactive Protein (4 Variables) (DAS28-4 [CRP]) at Day 14 (time frame: Baseline, Day 14). 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 22 Nov 2023.