Clinical trial
A First-in-human Phase I, Open-label, Multicentre, Dose Escalation Trial of BI 3819026 in Combination With Ezabenlimab in Patients With Unresectable Advanced or Metastatic Solid Cancers to Determine the Maximum Tolerated Dose (MTD) and Recommended Dose for Expansion (RDE)
NCT07607678 is registered in ClinicalTrials.gov with Boehringer Ingelheim as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A First-in-human Phase I, Open-label, Multicentre, Dose Escalation Trial of BI 3819026 in Combination With Ezabenlimab in Patients With Unresectable Advanced or Metastatic Solid Cancers to Determine the Maximum Tolerated Dose (MTD) and Recommended Dose for Expansion (RDE)
- Lead sponsor
- Boehringer Ingelheim
- Phase
- Phase 1
- Overall status
- Recruiting
- Start date
- May 1, 2026
- Completion date
- October 15, 2030
- Enrollment
- 60 (estimated)
- Sites
- 9
Conditions
As the registry lists them; a condition with its own page is linked.
advanced solid cancer, metastatic solid cancer