Efficacy and Safety of Filgotinib in the Treatment of Perianal Fistulizing Crohn's Disease
Status: | Recruiting |
---|---|
Conditions: | Crohns Disease |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 3/15/2019 |
Start Date: | April 6, 2017 |
End Date: | April 2020 |
Contact: | Gilead Clinical Study Information Center |
Email: | GileadClinicalTrials@gilead.com |
Phone: | 1-833-445-3230 (GILEAD-0) |
A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Efficacy and Safety of Filgotinib in the Treatment of Perianal Fistulizing Crohn's Disease
The primary objective of this study is to evaluate the efficacy of filgotinib as compared to
placebo in establishing combined fistula response at Week 24. Participants will have the
option to enter a separate long-term extension study if they meet eligibility requirements.
placebo in establishing combined fistula response at Week 24. Participants will have the
option to enter a separate long-term extension study if they meet eligibility requirements.
Key Inclusion Criteria:
- Males or non-pregnant, non-lactating females, ages 18 to 75 years, inclusive based on
the date of screening visit
- Diagnosis of Crohn's disease (CD) with a minimum duration of CD of at least 3 months
- Has draining perianal fistulae as a complication of CD, confirmed by MRI at screening
- Previously demonstrated an inadequate clinical response, loss of response to, or
intolerance of at least 1 of the following agents (depending on current country
treatment recommendations/guidelines):
- Antibiotics AND/OR
- Immunomodulators AND/OR
- TNFα Antagonist
- Is willing and able to undergo MRI per protocol requirements
- Is willing and able to undergo flexible sigmoidoscopy per protocol requirements
Key Exclusion Criteria:
- Presence of current rectovaginal anovaginal or enterovesicular fistulae
- Presence of ulcerative colitis (UC), indeterminate colitis, ischemic colitis,
fulminant colitis, or toxic mega-colon
- History of total proctocolectomy, total colectomy, presence of ileostomy or colostomy,
or likely requirement for surgery during the study
- Use of any prohibited concomitant medications as described in the study protocol
- Active tuberculosis (TB) or history of latent TB that has not been treated
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
We found this trial at
30
sites
3100 Duraleigh Road
Raleigh, North Carolina 27607
Raleigh, North Carolina 27607
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University of Maryland Medical Center Founded in 1823 as the Baltimore Infirmary, the University of...
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303 E Chicago Ave
Chicago, Illinois 60611
Chicago, Illinois 60611
(312) 503-8194
Northwestern University Feinberg School of Medicine Northwestern University Feinberg School of Medicine, founded in 1859,...
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601 East Rollins Street
Orlando, Florida 32803
Orlando, Florida 32803
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2093 Health Drive Southwest
Wyoming, Michigan 49519
Wyoming, Michigan 49519
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