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New immunotherapy combo aims to shrink lung tumors before surgery

NCT ID NCT07122687

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 33 times

Summary

This phase 2 trial tests whether adding an experimental immunotherapy (IBI363) or the approved drug Keytruda to chemotherapy before surgery can improve outcomes for people with stage IB to III non-squamous non-small cell lung cancer. About 170 participants will receive either IBI363 plus chemo or Keytruda plus chemo before their tumor is removed. The main goals are to see how many patients have no cancer left after treatment and to check for side effects.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Liaoning Cancer Hospital and Institute

    RECRUITING

    Shenyang, Liaoning, 110000, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

    Contact

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

IBI363 (an experimental immunotherapy) and pembrolizumab (Keytruda, an approved immunotherapy)

What this could lead to

If successful, this could offer a new treatment option before surgery for certain lung cancers, potentially improving survival and reducing recurrence.

What could go wrong

This is a mid-stage trial with only 170 participants. The experimental drug IBI363 may not work better than Keytruda, and side effects from combining immunotherapy with chemotherapy can be serious.

Conditions

The condition(s) this trial relates to.

non-small cell lung carcinoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.