Efficacy and Safety of Filgotinib in the Treatment of Small Bowel Crohn's Disease (SBCD)
Status: | Recruiting |
---|---|
Conditions: | Crohns Disease |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 4/3/2019 |
Start Date: | April 11, 2017 |
End Date: | March 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 Small Bowel Crohn's Disease (SBCD)
The primary objective of this study is to evaluate the efficacy of filgotinib, when compared
to placebo, in establishing clinical remission in participants with Crohn's disease involving
the small bowel. Participants will have the option to enter a separate long-term extension
study if they meet eligibility requirements.
to placebo, in establishing clinical remission in participants with Crohn's disease involving
the small bowel. 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, nonlactating females, ages 18 to 75 years, inclusive based on
the date of screening visit
- Moderately or severely active CD
- Minimum duration of CD of at least 6 months
- Presence of diseased SB segments in at least 1 of the following segments: terminal
ileum, distal ileum, or jejunum
- Patients with additional colonic involvement of CD are permitted in study as long as
SBCD is present
- Previously demonstrated an inadequate clinical response, loss of response to, or
intolerance to at least 1 of the following agents (depending on current country
treatment recommendations/guidelines):
- Corticosteroids
- Immunomodulators
- Tumor necrosis factor-alpha (TNFα) antagonists
- Vedolizumab
- Ustekinumab
- Willing and able to undergo magnetic resonance enterography (MRE) per protocol
requirements
Key Exclusion Criteria:
- Presence of symptomatic or clinically significant (eg, obstructive or symptomatic)
strictures or stenosis.
- Presence of fistulae
- Evidence of short bowel syndrome
- Presence of ulcerative colitis, indeterminate colitis, ischemic colitis, fulminant
colitis, or toxic mega-colon
- History of total colectomy, subtotal-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
28
sites
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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