Efficacy and Safety Trial of RPC1063 for Moderate to Severe Crohn's Disease

NCT02531113 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2021-01-22

Study results available
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Summary

The purpose is to determine whether RPC1063 is effective in the treatment of Crohn's disease.

Conditions

Interventions

DRUG

RPC1063

Sponsors & Collaborators

  • Celgene

    lead INDUSTRY

Principal Investigators

  • Kanthi Kollengode, MD · Celgene Corporation

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-09
Primary Completion
2019-09-12
Completion
2019-11-28

Countries

  • United States
  • Canada
  • Hungary
  • Poland
  • Ukraine

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02531113 on ClinicalTrials.gov