A Study of JNJ-86974680 in Participants With Advanced Non-small Cell Lung Cancer

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohnson & Johnson Enterprise Innovation Inc.

About this trial

The purpose of this study is to determine a safe and tolerable dose(s) of JNJ-86974680 for further research in combination with cetrelimab and radiation therapy.

Eligibility criteria

Qualifiers

Individuals with histologically or cytologically confirmed stage IIIB-IV non-small cell lung cancer (NSCLC)

Part 1: NSCLC with a known actionable genetic mutation (for example, epidermal growth factor receptor [EGFR], anaplastic lymphoma kinase [ALK], c-ros oncogene 1 [ROS1], v-raf murine sarcoma viral oncogene homolog B1 [BRAF]) must have received all approved targeted therapies and have progressed

Part 2: No targetable mutations (for example, EGFR [epidermal growth factor receptor], ALK [anaplastic lymphoma kinase], ROS1[c-ros oncogene 1], and BRAF [B-Raf proto-oncogene, serine/threonine kinase])

Part 1 and Cohort A of part 2: Must have been treated with (a) anti-programmed death protein 1 (anti-PD-1) or programmed cell death ligand 1 (PD-L1) therapy and (b) platinum-based chemotherapy

Disqualifiers

Active central nervous system (CNS) disease involvement

Active autoimmune disease

Active infection

History of solid organ or hematologic stem cell transplantation

Trial design

Treatments tested in this trial

  • JNJ-86974680
  • Cetrelimab
  • Radiation Therapy

Treatment groups

126 Participants
are divided into 2 treatment groups