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Tytuł pozycji:

Efficacy and Safety of PF-06651600 (Ritlecitinib), a Novel JAK3/TEC Inhibitor, in Patients With Moderate-to-Severe Rheumatoid Arthritis and an Inadequate Response to Methotrexate.

Tytuł:
Efficacy and Safety of PF-06651600 (Ritlecitinib), a Novel JAK3/TEC Inhibitor, in Patients With Moderate-to-Severe Rheumatoid Arthritis and an Inadequate Response to Methotrexate.
Autorzy:
Robinson MF; California Medical Research Associates, Northridge.
Damjanov N; University of Belgrade School of Medicine, Belgrade, Serbia.
Stamenkovic B; Institute for Treatment and Rehabilitation Niska Banja and Nis University School of Medicine, Nis, Serbia.
Radunovic G; University of Belgrade School of Medicine, Belgrade, Serbia.
Kivitz A; Altoona Center for Clinical Research, Duncansville, Pennsylvania.
Cox L; Pfizer, Inc., New York, New York.
Manukyan Z; Pfizer, Inc., New York, New York.
Banfield C; Pfizer, Inc., New York, New York.
Saunders M; Pfizer, Inc., New York, New York.
Chandra D; Pfizer, Inc., New York, New York.
Vincent MS; Pfizer, Inc., New York, New York.
Mancuso J; Pfizer, Inc., Groton, Connecticut.
Peeva E; Pfizer, Inc., New York, New York.
Beebe JS; Pfizer, Inc., New York, New York.
Źródło:
Arthritis & rheumatology (Hoboken, N.J.) [Arthritis Rheumatol] 2020 Oct; Vol. 72 (10), pp. 1621-1631. Date of Electronic Publication: 2020 Sep 07.
Typ publikacji:
Clinical Trial, Phase II; Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Malden, MA : Wiley, [2014]-
MeSH Terms:
Antirheumatic Agents/*therapeutic use
Arthritis, Rheumatoid/*drug therapy
Janus Kinase 3/*antagonists & inhibitors
Protein Kinase Inhibitors/*therapeutic use
Pyrimidines/*therapeutic use
Pyrroles/*therapeutic use
Adult ; Aged ; Antirheumatic Agents/adverse effects ; Double-Blind Method ; Female ; Humans ; Male ; Middle Aged ; Protein Kinase Inhibitors/adverse effects ; Pyrimidines/adverse effects ; Pyrroles/adverse effects ; Treatment Outcome
References:
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Molecular Sequence:
ClinicalTrials.gov NCT02969044
Substance Nomenclature:
0 (Antirheumatic Agents)
0 (PF-06651600)
0 (Protein Kinase Inhibitors)
0 (Pyrimidines)
0 (Pyrroles)
EC 2.7.10.2 (Janus Kinase 3)
Entry Date(s):
Date Created: 20200519 Date Completed: 20210106 Latest Revision: 20210110
Update Code:
20240105
PubMed Central ID:
PMC7589242
DOI:
10.1002/art.41316
PMID:
32419304
Czasopismo naukowe
Objective: To evaluate the efficacy and safety of PF-06651600 (ritlecitinib), an irreversible inhibitor of JAK3 and the tyrosine kinase expressed in hepatocellular carcinoma (TEC) kinase family, in comparison with placebo in patients with rheumatoid arthritis (RA).
Methods: An 8-week, phase II, double-blind, parallel-group study was conducted. Seventy patients who were seropositive for anti-citrullinated protein antibodies and/or rheumatoid factor were randomized 3:2 to receive oral PF-06651600 (200 mg once daily) or placebo for 8 weeks. Eligible patients had an inadequate response to methotrexate, and the study design allowed up to 50% of patients to have previously received 1 tumor necrosis factor inhibitor that was inadequately effective and/or not tolerated. The primary end point was change from baseline in the Simplified Disease Activity Index (SDAI) score at week 8, assessed by Bayesian analysis using an informative prior distribution for placebo response.
Results: Mean change from baseline in the SDAI score at week 8 was greater in the PF-06651600 group (-26.1 [95% credible interval -29.7, -22.4]) than in the placebo group (-16.8 [95% credible interval -20.9, -12.7]; P < 0.001). Most adverse events (AEs) were mild in severity, and no treatment-related serious AEs, severe AEs, or deaths were reported. The most common classes of AE were infections and infestations as well as skin and subcutaneous tissue disorders; there was 1 mild case of herpes simplex in the PF-06651600 group that was considered to be treatment related, which resolved within 3 days without study treatment discontinuation or antiviral therapy.
Conclusion: Treatment with the oral JAK3/TEC inhibitor PF-06651600 (200 mg once daily) was associated with significant improvements in RA disease activity and was generally well-tolerated in this small 8-week study.
(© 2020 Pfizer Inc. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.)

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