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87704916LUC1001 Lung cancer
INTRATUMORAL STUDY.

A Phase 1 study of intratumoral administration of JNJ-87704916 (oncolytic virus) as monotherapy and in combination for advanced solid tumors/mNSCLC

Phase
Compound
JNJ-87704916 (oncolytic virus) ± cetrelimab (anti–PD-1 mAb)
NCT identifier
NCT06311578
Enrollment

N=~96

For more information, including
contact details, please visit
the J&J Clinical Trial Finder
Study overview & design

Key eligibility criteria*:

  • Part 1: advanced solid tumors that have progressed on standard therapies
  • Parts 1 and 2: ≥1 injectable lesion
  • Part 2: ≥1 evaluable uninjected lesion
  • Part 2 Cohort A: mNSCLC without actionable mutations that have progressed on standard therapies
  • Part 2 Cohort B: previously untreated mNSCLC with PD-L1 ≥50%
Study design
Study design

Primary outcomes:

  • Selected dose
  • Safety

Secondary outcome:

  • Preliminary efficacy

*Not a complete list of inclusion and exclusion criteria. Not a complete list of outcomes.

1L, first line; 2L+, second line plus; IT, intratumoral; mNSCLC, metastatic non–small cell lung cancer; PD-L1, programmed cell death ligand 1.

Recruiting site locations
World Map
Canada, France, Spain, United States
Study design
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Intratumoral treatments in cancer
The safety and efficacy of these investigational agents have not been determined. There is no guarantee that the investigational agents listed will be filed with and/or approved for marketing by the FDA or local regulatory agencies.
For additional information you may visit www.clinicaltrials.gov.
Intratumoral treatments in cancer
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