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NCT06008093 · ClinicalTrials.gov registry record · Phase 3

A Study to Investigate the Efficacy of Durvalumab Plus Tremelimumab in Combination With Chemotherapy Compared With Pembrolizumab in Combination With Chemotherapy in Metastatic NSCLC Patients With Non-squamous Histology Who Have Mutations and/or Co-mutations in STK11, KEAP1, or KRAS

A Phase 3 study of Carcinoma, Non-Small Cell Lung, sponsored by AstraZeneca.

Recruiting
Registry status
Phase 3
Development phase
280
Enrollment target
20
Study locations

NCT06008093: Recruiting Phase 3 study of Carcinoma, Non-Small Cell Lung, sponsored by AstraZeneca.

NCT06008093 is a Phase 3 study of Carcinoma, Non-Small Cell Lung that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 280 participants, below the 322-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (13% lower). The trial reports 20 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06008093, a Phase 3 study of Carcinoma, Non-Small Cell Lung, is actively recruiting participants, sponsored by AstraZeneca.

RECRUITING
Registry status
Phase 3
Development phase
280 participants
Enrollment target
20
Study locations

Study Summary

The purpose of the study is to assess the efficacy of durvalumab plus tremelimumab in combination with chemotherapy compared with pembrolizumab in combination with chemotherapy in metastatic NSCLC patients with non-squamous histology who have mutations and/or co-mutations in STK11, KEAP1, or KRAS.

Primary Outcome

PFS is defined as the time from randomization until the date of confirmed PD (per Response Evaluation Criteria in Solid Tumours, Version 1.1 \[RECIST 1.1\] as assessed by the Investigator) or death due to any cause. The measure of interest is the hazard ratio (HR) and the corresponding 95% confidence interval (CI).

Interventions

  • DRUG Pembrolizumab
  • DRUG Carboplatin
  • DRUG Pemetrexed
  • DRUG Durvalumab
  • DRUG Tremelimumab

Study Locations (20)

California

  • Research Site - Beverly Hills
  • Research Site - Irvine
  • Research Site - La Jolla
  • Research Site - Loma Linda
  • Research Site - Los Alamitos
  • Research Site - Los Angeles
  • Research Site - Los Angeles
  • Research Site - Redding
  • Research Site - Santa Monica

Florida

  • Research Site - Fort Lauderdale
  • Research Site - Jupiter
  • Research Site - Ocala

Arizona

  • Research Site - Chandler
  • Research Site - Tucson

Colorado

  • Research Site - Denver
  • Research Site - Wheat Ridge

District of Columbia

  • Research Site - Washington D.C.
  • Research Site - Washington D.C.

Alabama

  • Research Site - Birmingham

Alaska

  • Research Site - Anchorage

Trial Details

FieldValue
Enrollment Target 280 participants
Start Date 2024-04-04
Est. Completion 2031-03-20
Phase Phase 3
AstraZeneca

1,285 total trials

What NCT06008093 shows while recruiting

NCT06008093 is an interventional study that assigns participants to a tested intervention. The registered 280 participants enrollment target is mid-sized for trials with a published cap, below the 322-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (13% lower).

The record links to 1 condition, with Carcinoma, Non-Small Cell Lung appearing as the primary indexed condition, and to 5 interventions - of which Pembrolizumab is the first listed.

NCT06008093 names 20 study sites across 7 states, led by California, Florida, Arizona.

Frequently Asked Questions

What is clinical trial NCT06008093 about?

NCT06008093 is a clinical study titled "A Study to Investigate the Efficacy of Durvalumab Plus Tremelimumab in Combination With Chemotherapy Compared With Pembrolizumab in Combination With Chemotherapy in Metastatic NSCLC Patients With Non-squamous Histology Who Have Mutations and/or Co-mutations in STK11, KEAP1, or KRAS". The purpose of the study is to assess the efficacy of durvalumab plus tremelimumab in combination with chemotherapy compared with pembrolizumab in combination with chemotherapy in metastatic NSCLC patients with non-squamous histology who have mutations and/or co-mutations in STK11, KEAP1, or KRAS.

What is the current status of trial NCT06008093?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 280 participants. The study started on 2024-04-04. Estimated completion is 2031-03-20.

What conditions does trial NCT06008093 study?

This clinical trial studies the following conditions: Carcinoma, Non-Small Cell Lung.

What interventions are being tested in trial NCT06008093?

The interventions under investigation include: Pembrolizumab (DRUG), Carboplatin (DRUG), Pemetrexed (DRUG), Durvalumab (DRUG), Tremelimumab (DRUG).

Who is sponsoring clinical trial NCT06008093?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06008093 being conducted?

This trial has 20 study locations across Alabama, Alaska, Arizona, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Carcinoma, Non-Small Cell Lung

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06008093's enrollment target sits among peer trials

280 44th of 130 higher than 87 of 130 other Carcinoma, Non-Small Cell Lung trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Carcinoma, Non-Small Cell Lung trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06008093, the US trial registry maintained by the National Library of Medicine. NCT06008093 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.