Phase 2 Lung Cancer Trial, Recruiting NCT06296745 Sponsor: Guangzhou Medical University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06296745
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 18 and 75 years, of any gender
  • People who have been diagnosed with non-small cell lung cancer (a type of lung cancer) confirmed through a tissue or cell sample, with a specific genetic change in the EGFR gene (either L858R or Exon19Del type)
  • People who have been diagnosed with leptomeningeal metastasis (cancer that has spread to the fluid and membranes surrounding the brain and spinal cord), confirmed according to established international medical guidelines
  • People whose cancer has continued to grow or spread after receiving double doses of a third-generation targeted therapy drug such as Osimertinib
  • People with normal liver and kidney function, and blood counts within acceptable ranges (confirm with trial site for exact values)
  • People with no history of severe nervous system disease
  • People with no severe blood or bone marrow disorders

Who may not be able to join:

  • People showing signs of serious nervous system failure, including severe brain dysfunction, significant white matter changes seen on brain scans, or a level of consciousness below a certain threshold (confirm with trial site)
  • People who have widespread, life-threatening disease in other parts of the body that is not responding to treatment
  • People who may have difficulty following the study requirements, or who have other reasons that make participation unsuitable as determined by the trial team

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Zhenyu Pan, Guangzhou Medical University

Phone: +8615804302753

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Guangzhou Medical University
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
20 January 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Clinical response rate; Neurological progression-free survival (NPFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov