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A Study of JNJ-1761981 in Participants With Solid Tumors
Sponsor: Johnson & Johnson Enterprise Innovation Inc.
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.
Official title: Phase 1 Study of Intratumoral Administration of JNJ-1761981 ER, an Extended Release Chemotherapy, in Participants With Solid Tumors
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
66
Start Date
2026-05-18
Completion Date
2029-01-31
Last Updated
2026-05-14
Healthy Volunteers
No
Conditions
Interventions
JNJ-1761981
JNJ-1761981 will be administered intratumorally.
Cetrelimab
Cetrelimab will be administered intravenously.
Locations (2)
Montefiore Medical Center
The Bronx, New York, United States
MD Anderson Cancer Center
Houston, Texas, United States