First line of the email MUST contain NCT # and Site #.
CONTACT
Lead
Bristol-Myers Squibb
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Participants with Ulcerative Colitis (UC) provided written consent to participate in the study
Participants who are aged ≥ 18 years at the earlier date of either initiation of treatment with ozanimod or azathioprine or obtaining consent
Starting dose of oral steroid ≥ 30 mg/day (prednisolone equivalent)
Administration of ozanimod or azathioprine started after oral steroid administration, and ozanimod or azathioprine administered concomitantly with steroids (excluding patients who started oral steroids and ozanimod or azathioprine on the same day)
In the ozanimod group, patients with notable clinical symptoms due to the primary disease (rectal bleeding subscore ≥ 1 point or total PRO2 score ≥ 2 points) remained at the start of ozanimod administration
In the azathioprine group, patients who started azathioprine treatment after February 2019
You may not be if
Participants with symptoms of UC with no change or increase in Patient-Reported Outcome 2 (PRO2) from the time of initiating oral steroid administration after 2 weeks of administration of ≥ 30 mg/day (prednisolone equivalent) of oral steroids
Participants with complications requiring continued steroid use (excluding topically acting steroids for inhalation or topical application)
Participants who participated in other clinical studies involving interventions during the observation period
Participants judged to be inappropriate for enrollment in this study by the investigator at each participating study site
Clareo Health | Effectiveness of Ozanimod in Patients With Steroid-Dependent Ulcerative Colitis
