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Clinical Trial ● Currently Recruiting Phase II NCT07470879

A Study of How the Medicine Called “Etrasimod” Works in Children With the Gut Disease Called Ulcerative Colitis

A Study of How the Medicine Called “Etrasimod” Works in Children With the Gut Disease Called Ulcerative Colitis — Recruiting • Phase II • Respiratory / COPD /…

📅 26 Jun 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT07470879
Sponsor
Pfizer
Start
2026-05-28
ClinicaliQ Trial Snapshot
  • A Study of How the Medicine Called “Etrasimod” Works in Children With the Gut Disease Called Ulcerative Colitis — Recruiting • Phase II • Respiratory / COPD / Asthma • NCT07470879.
  • Drug being tested: Etrasimod, a selective sphingosine-1-phosphate receptor modulator, is being evaluated for safety, efficacy, and pharmacokinetics in children aged 2 to <12 years with moderately to severely active ulcerative colitis.
  • Patient eligibility overview: The trial recruits paediatric patients (≥2 years to <12 years old) diagnosed with moderately to severely active ulcerative colitis, representing an understudied population in inflammatory bowel disease treatment.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The purpose of this study is to determine the safety, efficacy, and pharmacokinetics (PK) of etrasimod for the treatment of moderately to severely active ulcerative colitis in pediatrics participants (≥ 2 years up to < 12 years of age). Participants who will complete the total 52-week treatment period will have the opportunity to continue in a Long-Term Extension (LTE) Period of up to 4 years (5 years after study enrollment).

Eligibility Snapshot
  • : Have a diagnosis of ulcerative colitis (UC) that is moderately to severely active Participants are permitted to be receiving a therapeutic dose of select UC therapies

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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