Kwatra, Shawn G. http://orcid.org/0000-0003-3736-1515
Khattri, Saakshi
Amin, Ahmad Z.
Ranza, Roberto
Kaplan, Blair
Shi, Linyu
Padilla, Byron
Soliman, Ahmed M.
McGonagle, Dennis
Clinical trials referenced in this document:
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Documents that mention this clinical trial
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POS1545 MODULATION OF SERUM BIOMARKERS IN PATIENTS WITH PSA TREATED WITH RISANKIZUMAB IN THE PHASE 3 KEEPSAKE 2 STUDY
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POS1036 EFFICACY AND SAFETY OF RISANKIZUMAB (RZB) FOR ACTIVE PSORIATIC ARTHRITIS (PsA): 52-WEEK RESULTS FROM KEEPsAKE 2
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Improved patient-reported outcomes in patients with psoriatic arthritis treated with risankizumab: analysis of the Phase 3 trial KEEPsAKE 2
https://doi.org/10.1136/rmdopen-2022-002286
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https://doi.org/10.1136/annrheumdis-2021-221019
POS1032 RISANKIZUMAB FOR ACTIVE PSORIATIC ARTHRITIS: INTEGRATED SUBGROUP ANALYSIS FROM 2 DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE 3 STUDIES (KEEPsAKE 1 AND KEEPsAKE 2)
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https://doi.org/10.1136/annrheumdis-2021-221048
Population Pharmacokinetics and Exposure–Response Analyses for Risankizumab in Patients with Active Psoriatic Arthritis
https://doi.org/10.1007/s40744-022-00495-0
POS1057 IMPACT OF RISANKIZUMAB ON ENTHESITIS AND ASSOCIATED PAIN: POOLED RESULTS FROM THE PHASE 3, RANDOMIZED, DOUBLE-BLIND KEEPsAKE 1 AND 2 TRIALS
https://doi.org/10.1136/annrheumdis-2022-eular.3161
AB0905 Routine Assessment of Patient Index Data 3 (RAPID3) in Patients With Active Psoriatic Arthritis (PsA) After Inadequate Response or Intolerance to DMARDs: Pooled Results From the Phase 3, Randomized, Double-Blind KEEPsAKE 1 and 2 Trials
https://doi.org/10.1136/annrheumdis-2022-eular.2913
Article History
Received: 31 January 2024
Accepted: 19 April 2024
First Online: 13 May 2024
Declarations
:
: Shawn G. Kwatra is an advisory board member/consultant and/or investigator for AbbVie, Arcutis, ASLAN, Celldex, Galderma, Genzada, Incyte, J&J, Novartis, Pfizer, Regeneron, and Sanofi. Saakshi Khattri is a speaker, serves as an advisory board member for, and/or has received research grants from AbbVie, BMS, Janssen, LEO, Lilly, Novartis, Pfizer, and UCB. Ahmad Z. Amin has received speaker or consulting fees from AbbVie, Amgen, BMS, Dermavant, Incyte, Janssen, LEO, Lilly, Regeneron, Sanofi-Genzyme, Pfizer, and UCB. Roberto Ranza is a consultant for AbbVie, Janssen, Novartis, and Pfizer, and is a member of speaker bureaus for AbbVie, Janssen, Novartis, and Pfizer. Blair Kaplan, Linyu Shi, Byron Padilla, and Ahmed M. Soliman are employees of AbbVie, and may hold AbbVie stock, stock options, and/or patents. Dennis McGonagle has received research grants from and/or is a member of speaker bureaus for AbbVie, BMS, Celgene, Janssen, Lilly, Novartis, Pfizer, and UCB.
: The clinical trials were conducted in accordance with the operations manual, protocol, International Council for Harmonisation guidelines, and applicable guidelines and regulations governing ethical principles and study conduct originating in the Declaration of Helsinki. Independent ethics committees/institutional review boards ensured the ethical, scientific, and medical appropriateness of the study before it was conducted and approved all relevant documentation including the protocol, informed consent form(s), and all participant materials. Written informed consent was obtained from all patients before enrollment.