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NCT07680764 · ClinicalTrials.gov registry record · Phase 2

A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment for Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

A Phase 2 study, sponsored by Bristol-Myers Squibb.

Not yet
Registry status
Phase 2
Development phase
160
Enrollment target

NCT07680764: Clinical Trial Phase 2 study, sponsored by Bristol-Myers Squibb.

NCT07680764 is a Phase 2 study that has not yet begun recruiting, run by Bristol-Myers Squibb. The registered enrollment target is 160 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07680764, a Phase 2 study, has not yet begun recruiting, sponsored by Bristol-Myers Squibb.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
160 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety, tolerability, and efficacy of Imzokitug in combination with Pumitamig and Platinum-Doublet Chemotherapy (PDCT) versus Pumitamig and PDCT as first-line treatment for participants with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

Interventions

  • DRUG Pumitamig
  • DRUG Imzokitug

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2026-08-15
Est. Completion 2030-09-15
Phase Phase 2
Bristol-Myers Squibb

1,025 total trials

What is known before NCT07680764 opens enrollment

NCT07680764 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 2 interventions - of which Pumitamig is the first listed.

NCT07680764 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07680764 about?

NCT07680764 is a clinical study titled "A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment for Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)". The purpose of this study is to assess the safety, tolerability, and efficacy of Imzokitug in combination with Pumitamig and Platinum-Doublet Chemotherapy (PDCT) versus Pumitamig and PDCT as first-line treatment for participants with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

What is the current status of trial NCT07680764?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 160 participants. The study started on 2026-08-15. Estimated completion is 2030-09-15.

What interventions are being tested in trial NCT07680764?

The interventions under investigation include: Pumitamig (DRUG), Imzokitug (DRUG).

Who is sponsoring clinical trial NCT07680764?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07680764's enrollment target sits among peer trials

160 422nd of 2000 higher than 1,559 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT07680764, the US trial registry maintained by the National Library of Medicine. NCT07680764 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.