The purpose of this open-label extension (OLE) study is to evaluate the safety and efficacy of etrasimod in participants with moderately to severely active ulcerative colitis (UC) who previously received double-blind treatment (either etrasimod 2 mg per day or placebo) during participation in one of the qualified Phase 3 or Phase 2 double-blind, placebo-controlled parent studies including but not limited to: (APD334-301 [NCT03945188] or APD334-302 [NCT03996369] or APD334-210 [NCT04607837]).
Condition | Ulcerative Colitis |
---|---|
Treatment | Etrasimod |
Clinical Study Identifier | NCT03950232 |
Sponsor | Arena Pharmaceuticals |
Last Modified on | 13 October 2022 |
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