Phase 3 Lung Cancer Trial, Recruiting NCT06875310 Sponsor: Mirati Therapeutics Inc. Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT06875310
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 a specific type of lung cancer (non-squamous non-small cell lung cancer) that has been confirmed by a tissue or cell sample, and whose cancer has a particular genetic change called a KRAS G12C mutation (found in a tumour sample or a blood test).
  • People whose lung cancer has spread to nearby areas or to other parts of the body.
  • People whose cancer has at least one measurable tumour, as seen on a CT or MRI scan.
  • People who have not yet received any systemic (whole-body) anti-cancer treatment for their advanced or metastatic disease.
  • People for whom curative treatments such as surgery or combined chemotherapy and radiation are not considered appropriate options by their treating doctor.
  • People who have cancer that has spread to the brain may still be considered, including those whose brain tumours have not yet been treated, provided the brain tumours are causing no symptoms, do not need urgent treatment, and are no larger than 20mm in size.
  • People whose tumours show any level of a protein called PD-L1 (from 0% to 100%), as measured by one of three specified approved laboratory tests.

Who may not be able to join:

  • People who have an active autoimmune or inflammatory condition that has required systemic (whole-body) medical treatment at any point in the past two years.
  • People who have had significant or uncontrolled heart or blood vessel problems within the past six months, or where there is an ongoing risk of those problems returning.
  • People whose blood test results show that bone marrow or liver function is not at an adequate level, or whose heart rhythm test (ECG) shows certain abnormalities.
  • People who are currently taking medications known to affect heart rhythm in a specific way (called QTc prolongation) and for whom switching to a different medication before joining the trial is not possible.
  • People who have previously received any treatment that specifically targets the KRAS G12C mutation, such as sotorasib or adagrasib, in any context.
  • People who have another serious ongoing medical, psychiatric, or laboratory condition that the trial team considers would increase the risks associated with taking part.
  • Additional criteria defined in the full trial protocol also apply (confirm with trial site).

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 8 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

Principal Investigator: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

Australian sites

Canberra Hospital, Canberra, Australian Capital Territory
610251242220
Tamworth Hospital, North Tamworth, New South Wales
0267677760
Orange Hospital, Orange, New South Wales
61263693380
Princess Alexandra Hospital, Brisbane, Queensland
0731766505
Lyell McEwin Hospital, Elizabeth Vale, South Australia
0433217127
Frankston Hospital, Frankston, Victoria
61397847777
Northern Hospital, Melbourne, Victoria
0434 479 184
Latrobe Regional Health, Traralgon, Victoria
03 5173 8000
Joondalup Health Campus, Joondalup, Western Australia
61863889681

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
Mirati Therapeutics Inc.
Registry
ClinicalTrials.gov
Start date
24 April 2025
Est. completion
7 September 2029

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇦 Canada 🇨🇱 Chile 🇨🇳 China 🇨🇴 Colombia 🇭🇷 Croatia 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece Hong Kong 🇭🇺 Hungary 🇮🇳 India 🇮🇪 Ireland 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇲🇽 Mexico 🇳🇱 Netherlands 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇦 Saudi Arabia 🇰🇷 South Korea 🇪🇸 Spain 🇨🇭 Switzerland 🇹🇼 Taiwan 🇹🇭 Thailand Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Progression Free Survival (PFS) as Assessed per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by Blinded Independent Central Review (BICR); Overall Survival (OS)

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: 8 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