Last updated on July 2019

Open-Label Extension of RPC1063 as Therapy for Moderate to Severe Ulcerative Colitis


Brief description of study

The purpose of this study is to determine the long-term safety of RPC1063 for the treatment of all patients with moderate to severe Ulcerative Colitis (UC) as well as the long-term efficacy of RPC1063 for the treatment of adult patients with moderate to severe UC. Additionally, to determine the long-term efficacy of RPC1063 for the treatment of adolescent patients with moderate to severe UC.

Detailed Study Description

The trial is an open label extension study. Eligible patients from the RPC01-3101 and RPC01-202 trials will have the option to enroll in this trial to receive study medication until the end of 2021 or until marketing approval of RPC1063 for UC is obtained in their country, or until the Sponsor discontinues the development program, whichever comes first.

Clinical Study Identifier: NCT02531126

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Beavercreek, OH United States
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Oklahoma City, OK United States
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Germantown, TN United States
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Virginia Beach, VA United States
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Buenos Aires, Argentina
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