Lung Cancer Trial, Recruiting NCT06809764 Sponsor: Daiichi Sankyo Condition: Lung Cancer
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Lung Cancer Trial, Recruiting

NCT06809764
Recruiting Not Applicable

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 who are 18 years of age or older at the time of signing the consent form
  • People who have been diagnosed with a type of lung cancer called non-squamous non-small cell lung cancer (NSCLC) that cannot be removed by surgery and/or has spread to other parts of the body
  • People whose lung cancer has a specific genetic change (mutation) in a gene called HER2 that is known to drive cancer growth
  • People who have a general health/activity level rated as 0, 1, or 2 on a standard medical scale (meaning able to carry out some or all daily activities) (confirm with trial site)
  • People who are receiving, or have very recently started (within the last 2 months), a treatment called T-DXd, based on their doctor's decision

Who may not be able to join:

  • People who have previously been treated with certain HER2-targeted therapies, including specific medicines that block HER2 signals (called tyrosine kinase inhibitors targeting HER2 mutations — though a broader class called pan-HER TKIs may be acceptable), or antibody-drug treatments (ADCs) that carry a particular type of chemotherapy agent (confirm with trial site)
  • People who have spinal cord compression, or brain/nervous system cancer spread that is untreated and causing symptoms, or that requires steroid or anti-seizure medicines to manage symptoms
  • People who have serious or poorly controlled overall health conditions, such as uncontrolled high blood pressure or active uncontrolled bleeding problems

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Project Manager, Daiichi Sankyo Co., Ltd.

Phone: 908-992-6400

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
Not Applicable
Sponsor
Daiichi Sankyo
Registry
ClinicalTrials.gov
Start date
21 February 2025
Est. completion
12 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival (PFS) by Investigator Assessment in Real-world Setting (rwPFS)

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