A Study of Zasocitinib (TAK-279) in Adults With Active Crohn's Disease

Starting soon · Phase 2

Conditions studied: Crohn's Disease

In brief

Crohn's disease (CD) is a serious, long-term condition that can cause swelling (inflammation) and painful ulcers anywhere in the gut. This study will investigate whether zasocitinib can improve CD biology at the cellular and molecular level in adults. The main aims of this study are to better understand zasocitinib's mechanism of action in CD and evaluate how safe this treatment is. The participants will be treated with zasocitinib for 3 months (12 weeks) and will need to undergo a test where a doctor uses a thin, flexible tube with a tiny camera to look inside the large bowel (colon) and the end of the small bowel (ileum); this test is called ileocolonoscopy. During the study, participants will visit the study clinic several times.

Key facts

Study ID

NCT07403968

Run by

Takeda

People needed

20

Starts

2026-07-15

Expected to finish

2028-03-30

Last updated by the study team

2026-07-01

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men and women aged 18 to 75 years can participate in the study.
• Must have been diagnosed with Crohn's disease (CD) at least 1 month (30 days) before study start.
• Must have received other treatments for CD earlier but no longer tolerate these treatments or the treatment no longer helps.

You may not qualify if…

• Cannot have another condition that causes swelling (inflammation) in the bowel.
• Cannot have complications of CD which may require surgery.
• Cannot have current abscesses or abscesses that have been treated within 6 weeks before study start.
• Cannot have had a removal of parts of the bowel within half a year (6 months) before study start.
• Cannot have had any surgery inside the belly (intraabdominal) within 3 months before study start.
• Cannot have or had a J-pouch.
• Cannot have had infections up to 2 months (8 weeks) before study start.
• Cannot have given blood or plasma within 1 month (30 days) before study start.
• Cannot tolerate having blood taken with a needle from a vein (venipuncture).
• Additional entry criteria will be discussed with the study doctor.

Full record on ClinicalTrials.gov

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