Study of DCC-2618 in Patients With GIST After at Least 3 Prior Treatments
Recruiting now · Phase 1
Conditions studied: Gastrointestinal Stromal Tumors
In brief
To evaluate the safety of DCC-2618 in patients with unresectable, metastatic, or recurrent gastrointestinal stromal tumor (GIST) who have received three or more prior therapies
Key facts
- Study ID
- NCT07618377
- Run by
- Ono Pharmaceutical Co., Ltd.
- People needed
- 10
- Starts
- 2026-07-07
- Expected to finish
- 2028-02-01
- Last updated by the study team
- 2026-07-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participants with a histologically confirmed diagnosis of GIST.
- Participants who are refractory or intolerant to treatment with at least imatinib, sunitinib, and regorafenib.
- Participants with at least one measurable lesion per the modified Response Evaluation Criteria in Solid Tumors (mRECIST) within 28 days prior to the first administration of the investigational product.
- Participants with an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1.
You may not qualify if…
- Participants with a concomitant or prior history of severe hypersensitivity reactions to other tyrosine kinase inhibitors.
- Participants with uncontrolled diabetes mellitus.
- Participants with a systemic infection requiring treatment.
Where it is running
- National Cancer Center Hospital East — Kashiwa, Chiba, Japan (enrolling)
- National Cancer Center Hospital — Tokyo, Chuo-ku, Japan (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.