A Study of JNJ-90301900 in Combination With Chemoradiation Followed by Consolidation Immunotherapy for Non-Small Cell Lung Cancer (NSCLC)
NCT06667908 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 130
Last updated 2026-05-11
Summary
The purpose of this study is to determine whether JNJ-90301900 added to concurrent platinum-based doublet chemotherapy with radiation therapy (cCRT) followed by consolidation immunotherapy (cIT) can improve objective response rate (ORR; that is percentage of participants whose best response is complete response or partial response during the study) in participants with locally advanced and unresectable stage III non-small cell lung cancer.
Conditions
- Carcinoma, Non-Small-Cell Lung
Interventions
- DRUG
-
JNJ-90301900
JNJ-90301900 will be injected intratumorally and/or intranodally.
- BIOLOGICAL
-
Durvalumab will be administered as intravenous (IV) infusion as cIT.
- RADIATION
-
Concurrent Chemo/Radiation Therapy (cCRT)
Radiation by intensity modulated radiation therapy (IMRT) will be administered.
- DRUG
-
Concurrent Chemo/Radiation Therapy (cCRT): Carboplatin
Carboplatin will be administered as IV infusion as platinum-based doublet chemotherapy.
- DRUG
-
Concurrent Chemo/Radiation Therapy (cCRT): Paclitaxel
Paclitaxel will be administered as IV infusion as platinum-based doublet chemotherapy.
Sponsors & Collaborators
-
Johnson & Johnson Enterprise Innovation Inc.
lead INDUSTRY
Principal Investigators
-
Johnson & Johnson Enterprise Innovation Inc. Clinical Trial · Johnson & Johnson Enterprise Innovation Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-12-06
- Primary Completion
- 2028-12-31
- Completion
- 2028-12-31
- FDA Drug
- Yes
Countries
- United States
- Australia
- Brazil
- China
- France
- Hong Kong
- Netherlands
- Spain
- Turkey (Türkiye)
- United Kingdom
Study Locations
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