Clinical Trial

A Study of JNJ-1761981 in Participants With Solid Tumors

Recruiting Phase 1
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Summary
The purpose of Part 1 of this study is to determine a safe, tolerable, and feasible recommended total dose of intratumorally administered JNJ-1761981. The purpose of Part 2 of this study is to identify the optimal volumetric dose of JNJ-1761981 for the treatment of tumor lesions.
Protocol Amendment History 1 change
critical Recruitment opened 2026-05-15
Trial Details
NCT Number NCT07525141
Lead Sponsor Johnson & Johnson Enterprise Innovation Inc.
Conditions Neoplasms
Enrollment 66 participants
Start Date 2026-05-18
Primary Completion 2028-01-12 (estimated)
Study Completion 2029-01-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-06