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Study details
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A Study of JNJ-90301900 in Combination With Chemoradiation Followed by Consolidation Immunotherapy for Non-Small Cell Lung Cancer (NSCLC)

Johnson & Johnson Enterprise Innovation Inc.
NCT IDNCT06667908ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

130

Study length

about 4.1 years

Ages

18+

Locations

15 sites in CT, FL, GA +8

What this study is about

Researchers are testing whether adding a treatment to chemotherapy and radiation therapy, followed by immunotherapy, can improve the response rate in people with advanced lung cancer. The trial will last about 1486 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Concurrent Chemo/Radiation Therapy (cCRT)
  • 2.Receive Durvalumab
  • 3.Take Concurrent Chemo/Radiation Therapy (cCRT): Carboplatin
  • +2 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

chemotherapy, durvalumab

Drug routes

infusion

Endpoints

Primary: Objective Response Rate (ORR) Using Independent Central Review (ICR) Assessment

Secondary: Disease Control Rate (DCR) Post-cCRT and Pre-cIT, Duration of Response (DoR), Number of Participants Reporting Laboratory Parameters, Physical Examination, Vital Signs Including Eastern Cooperative Oncology Group (ECOG) Performance Status Abnormalities, Number of Participants with Treatment-Emergent Adverse Event (TEAE) Related to Study Treatment, Objective Response Rate (ORR) Post-cCRT and Pre-cIT, Objective Response Rate (ORR) as Assessed by the Investigator, Progression Free Survival (PFS)

Procedures

radiation

Body systems

Oncology