Abstract

Ozanimod as a novel oral small molecule therapy for the treatment of Crohn's disease: The YELLOWSTONE clinical trial program

Contemp Clin Trials. 2022 Nov;122:106958.doi: 10.1016/j.cct.2022.106958. Epub 2022 Oct 5.

 

Brian G Feagan 1Stefan Schreiber 2Anita Afzali 3Florian Rieder 4Jeffrey Hyams 5Kanthi Kollengode 6Jared Pearlman 6Vladimir Son 6Cecilia Marta 6Douglas C Wolf 7Geert G D'Haens 8

 
     

Author information

1Western University, London, Ontario, Canada. Electronic address: brian.feagan@alimentiv.com.

2Department of Internal Medicine I, University Hospital Schleswig-Holstein, Kiel University, Kiel, Germany.

3Division of Digestive Diseases, University of Cincinnati, Cincinnati, OH, USA.

4Department of Gastroenterology, Hepatology, and Nutrition, Digestive Diseases and Surgery Institute, Cleveland Clinic, Cleveland, OH, USA.

5Connecticut Children's Medical Center, Hartford, CT, USA.

6Bristol Myers Squibb, Princeton, NJ, USA.

7Center for Crohn's Disease & Ulcerative Colitis, Atlanta Gastroenterology Associates, Atlanta, GA, USA.

8Inflammatory Bowel Disease Center, Amsterdam University Medical Centers, Amsterdam, Netherlands.

Abstract

Background: Ozanimod, an oral sphingosine 1-phosphate receptor modulator currently approved for the treatment of moderately to severely active ulcerative colitis and relapsing multiple sclerosis, showed clinical, endoscopic, and histological benefit in the phase 2 STEPSTONE trial for Crohn's disease (CD). We aim to describe the trial design of the YELLOWSTONE phase 3 program evaluating the safety and efficacy of ozanimod in patients with moderately to severely active CD.

Methods: The YELLOWSTONE program consists of phase 3, randomized, double-blind, placebo-controlled induction (NCT03440372 and NCT03440385) and maintenance (NCT03464097) trials and an open-label extension (OLE) study (NCT03467958). Patients with inadequate response or intolerance to ≥1 CD treatment are randomized to receive daily ozanimod 0.92 mg (equivalent to ozanimod HCl 1 mg) or placebo for 12 weeks during induction. Those who respond to ozanimod are rerandomized to continue ozanimod or placebo maintenance therapy for 52 weeks. Patients who do not meet criteria for maintenance, experience relapse during maintenance, or complete maintenance or ≥ 1 year of STEPSTONE are eligible for open-label treatment for up to 234 weeks. Efficacy endpoints include clinical, endoscopic, and histologic outcomes.

Results: Expected 2023 (induction studies), 2024 (maintenance study), and 2026 (OLE).

Conclusion: YELLOWSTONE will provide pivotal phase 3 data on the safety and efficacy of ozanimod in patients with moderately to severely active CD using state-of-the-art methods, including centrally read endoscopic and histologic measurements, along with subjective assessments of symptom control based on the Crohn's Disease Activity Index. These studies could enable approval of ozanimod as a new CD therapy.

Clinical trial registration numbers: NCT03440372NCT03440385NCT03464097NCT03467958.

 

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