Clinical Trial of N-803 Plus Tislelizumab or Prior Failed Immune Checkpoint Inhibitor and Docetaxel Versus Docetaxel Monotherapy in Participants With Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Acquired Resistance to Immune Checkpoint Inhibitor Therapy

NCT06745908Phase 3Recruiting

Lead sponsor
ImmunityBio, Inc. (Industry)
Enrollment
507 (estimated)
Start date
1 Oct 2025
Primary completion
Sep 2028 (estimated)
Study completion
1 Jan 2029
Last update posted
2 Nov 2026

Design

Study type
Interventional
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel
Masking
None
Arms
4

Interventions

  • N-803 Drug
  • Tislelizumab Drug
  • Docetaxel Drug
  • Prior failed checkpoint inhibitor Drug

Conditions and primary outcome

  • NSCLC Stage IV

Primary outcome

Compare Overall Survival between the experimental and control arms (Approximately 12 months)

Posted results on ClinicalTrials.gov

Results posted on ClinicalTrials.gov: No

Results from company and journal sources

No editor-confirmed results are on record for this study.

Publications

No PubMed citation lists NCT06745908.

CT-VCA trial quality

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Data integrity

Compare what the registry, company releases, FDA documents and publications say about this study.

Drugs on HealthTrade

Source

Source: ClinicalTrials.gov, U.S. National Library of Medicine. Listing a study does not mean NLM has evaluated it.

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