Phase 3 Lung Cancer Trial, Recruiting NCT06692738 Sponsor: AstraZeneca Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT06692738
Recruiting Phase 3 🇦🇺 Australian site

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 have been diagnosed with squamous non-small cell lung cancer (a specific type of lung cancer), confirmed by a laboratory test on a tissue or cell sample.
  • People whose lung cancer has spread to other parts of the body (Stage IV) and cannot be treated with the aim of a cure.
  • People whose cancer testing has not found any specific gene changes (mutations) for which there are already approved targeted treatments available locally.
  • People whose tumor sample shows a certain level of a protein called PD-L1 (at least 1% of tumor cells), confirmed by an acceptable tissue sample provided to the trial.
  • People who have at least one measurable tumor that has not been previously treated with radiation, large enough to be accurately measured by CT or MRI scan.
  • People whose organs (such as kidneys and liver) and bone marrow are functioning well enough to meet the trial's requirements.

Who may not be able to join:

  • People whose lung cancer includes certain subtypes called small cell or neuroendocrine components.
  • People who have cancer that has spread to the brain, unless those brain metastases are not causing symptoms, are stable, and have not required steroids or seizure medications for at least 7 days before joining — and at least 2 weeks must have passed since any brain radiation or surgery, with full recovery from side effects (confirm with trial site).
  • People who have previously received any systemic (whole-body) treatment for advanced or metastatic lung cancer.
  • People who have previously been treated with a type of immunotherapy known as an anti-PD-1 or anti-PD-L1 drug.
  • People who have previously received a treatment targeting a pathway called TIGIT, or any other cancer therapy that works by targeting immune-regulatory pathways.
  • People with a history of another cancer diagnosis, unless that cancer was treated with the aim of a cure, has shown no signs of returning for at least 2 years, and is considered low risk for coming back.
  • People with active or previously diagnosed autoimmune or inflammatory conditions that have required ongoing treatment with steroids or other immune-suppressing medications.
  • People with an active condition that weakens the immune system, or an active serious infection.
  • People with an active tuberculosis infection.

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 13 July 2026
Phase 3: approximately ~65% 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

Phone: 1-877-240-9479

Australian sites

Research Site, Darlinghurst,
Research Site, Hyde Park,
Research Site, Southport,
Research Site, Wollongong,

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 3
Sponsor
Registry
ClinicalTrials.gov
Start date
18 November 2024
Est. completion
5 February 2029

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇳 India 🇮🇹 Italy 🇯🇵 Japan 🇲🇾 Malaysia 🇳🇱 Netherlands 🇵🇪 Peru 🇵🇱 Poland Puerto Rico 🇰🇷 South Korea 🇪🇸 Spain 🇹🇼 Taiwan 🇹🇭 Thailand Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States 🇻🇳 Vietnam

4 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Overall survival (OS); Progression-free survival (PFS)

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: 13 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