Phase 2 Lung Cancer Trial, Recruiting NCT07659782 Sponsor: Verastem, Inc. Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07659782
Recruiting Phase 2

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not 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 may be able to join

  • A pathology test has confirmed a diagnosis of non-small cell lung cancer (NSCLC) that cannot be surgically removed and has either spread to nearby areas or to other parts of the body.
  • The cancer has at least one measurable area of disease, as determined by a standard measurement system called RECIST 1.1.
  • Testing on tumour tissue has confirmed a specific genetic change in the cancer called a KRAS G12D mutation, and tissue is available for further confirmatory testing at a central laboratory.
  • The person has a good general level of physical functioning, rated 0 or 1 on a standard scale used by doctors (meaning fully active or able to carry out light activity).
  • The person's organs (such as kidneys, liver, and bone marrow) are functioning at an adequate level.
  • The person has previously been treated with both a platinum-based chemotherapy and an immune checkpoint inhibitor for advanced or unresectable disease.
  • The cancer has been documented to have gotten worse during or after the most recent treatment received.
  • For people being considered for the 2nd or 3rd line of treatment (without brain involvement), on a stable or preferred dose: at least 1 but no more than 2 prior treatment regimens have been received for advanced or unresectable NSCLC.
  • For people being considered for the 2nd to 4th line of treatment who have cancer that has spread to the brain: at least 1 but no more than 3 prior treatment regimens have been received for advanced or unresectable NSCLC.
  • For people with brain metastases: the brain metastases are not causing symptoms and have not yet been treated.
  • For people with brain metastases: at least one untreated, measurable brain lesion meets specific size requirements (longest measurement at least 0.5 cm and no more than 3 cm) under a specific measurement system (confirm with trial site).

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • The person has another documented mutation in a group of genes related to RAS (other than the KRAS G12D mutation being studied).
  • The person has received any anti-cancer treatment within 4 weeks before the first dose of the trial treatment, or within a drug-specific timeframe — whichever is shorter.
  • The person has had major surgery within 4 weeks before the first dose of the trial treatment.
  • The person has received radiation therapy within 1 week before the first dose of the trial treatment.
  • The person has a history of lung inflammation or scarring caused by a medication (known as drug-induced interstitial lung disease).
  • The person has previously received a treatment that directly targets the RAS protein.
  • The person has cancer that has spread to the brain and is either causing symptoms or has not yet been treated (note: people with untreated brain metastases may be eligible under the specific brain metastases group described above — confirm with trial site).
  • The person has taken certain medications that strongly affect how the body processes drugs (called strong CYP3A4 inhibitors, inducers, or sensitive substrates with a narrow therapeutic index) within 14 days before the first dose, or within a drug-specific timeframe — whichever is shorter (confirm with trial site).
  • The person has taken a proton pump inhibitor (a common type of heartburn or acid reflux medication) or an H2 blocker (another type of acid-reducing medication) within 5 days before the first dose.
  • The person is unable to swallow oral (by mouth) medication.
  • There may be additional criteria not listed here that the trial site will assess.

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 15 July 2026

Contact this trial

Phone: 7812924204

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

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Verastem, Inc.
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
1 June 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Confirmed ORR by blinded independent central review (BICR) per RESIST v1.1; To characterize the safety and tolerability of VS-7375 monotherapy administered on a daily oral schedule in participants with KRAS G12D-mutated NSCLC

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: 15 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