Phase 1 Study of Intratumoral Administration of JNJ-87704916, an Oncolytic Virus, as Monotherapy and in Combination for Advanced Solid Tumors
Johnson & Johnson Enterprise Innovation Inc.
Summary
The purpose of this study is to determine the safety, feasibility, recommended dose(s) and regimen(s) of JNJ-87704916 as monotherapy and in combination with cetrelimab.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * For Part 1: Individuals with a diagnosis of advanced or metastatic solid tumor exhausting all available standard of care therapy; Part 2: Individuals with histologically or cytologically confirmed metastatic or locally advanced NSCLC * Have at least 1 injectable tumor * Eastern cooperative oncology group (ECOG) performance status of grade 0 or 1 * A participant who can have children must have a negative pregnancy test before the first dose of study treatment and during the study * Thyroid function laboratory values within normal range except for participants on thyroid h…
Interventions
- DrugJNJ-87704916
JNJ-87704916 will be administered as an intratumoral injection.
- DrugCetrelimab
Cetrelimab will be administered.
- DrugStandard of Care PD(L)-1
Frontline anti-PD(L)-1 antibody therapy will be administered as standard of care treatment.
Locations (10)
- NYU Langone HealthNew York, New York
- Fox Chase Cancer CenterPhiladelphia, Pennsylvania
- UPMC Cancer CentersPittsburgh, Pennsylvania
- MD Anderson Cancer CenterHouston, Texas
- Toronto General HospitalToronto, Ontario
- Centre Hospitalier de l'Universite de MontrealMontreal, Quebec