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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
2026-07-06
Healthy Volunteers
No
Conditions
Interventions
JNJ-1761981
JNJ-1761981 will be administered intratumorally.
Cetrelimab
Cetrelimab will be administered intravenously.
Locations (4)
Mayo Clinic in Florida
Jacksonville, Florida, United States
Mayo Clinic Rochester
Rochester, Minnesota, United States
Montefiore Medical Center
The Bronx, New York, United States
MD Anderson Cancer Center
Houston, Texas, United States