Phase 2 Parkinson's Disease Trial, Recruiting
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:
- You have been diagnosed with advanced or metastatic non-squamous non-small cell lung cancer (a specific type of lung cancer that has spread), confirmed by a lab test on tissue or cells
- Your tumor or a blood test has shown a specific genetic change called a KRAS G12C mutation
- You are able to provide either a previously stored tumor tissue sample or a new tissue sample taken from a tumor that has not been treated with radiation
- Any side effects from previous cancer treatments have mostly gone away (back to mild or baseline levels), with some exceptions for nerve-related or hormone-related side effects
- If you have HIV, it is well controlled with medication
- If you have hepatitis B, you have been on antiviral treatment for at least 4 weeks and the virus is undetectable in your blood
- If you have hepatitis C, the virus is undetectable in your blood
Who may not be able to join:
- You have been diagnosed with small cell lung cancer, or your tumor contains small cell elements
- You have HIV and have also had a condition called Kaposi's sarcoma or Multicentric Castleman's Disease
- You have an active inflammatory bowel condition (such as Crohn's disease or ulcerative colitis) that requires immune-suppressing medication, or you have a clear history of such a condition
- You have serious uncontrolled heart or blood vessel problems — such as severe heart failure, unstable chest pain, a recent heart attack, uncontrolled irregular heartbeat, or certain abnormal heart rhythm readings — within the past 6 months
- You have previously received any systemic (whole-body) cancer treatment for advanced or metastatic non-small cell lung cancer
- You previously received immunotherapy and had to stop it because of a serious immune-related side effect (grade 3 or higher), or had to stop due to heart inflammation or recurring lung inflammation
- You have previously received any treatment that specifically targets the KRAS gene mutation
- You have received cancer treatment within the past 4 weeks (or within 5 half-lives of the drug, whichever is shorter) and have not recovered from its side effects
- You have received high-dose radiation to the lung within the past 6 months
- You have an immune system disorder, or you are taking steroid medications at higher than a low daily dose, or other immune-suppressing drugs within the past 7 days
- You have another cancer that is still growing or has needed active treatment within the past 3 years
- You have active cancer that has spread to the brain or the lining around the brain or spinal cord
- You have an active autoimmune disease (where the body attacks itself) that has needed treatment in the past 2 years (hormone replacement therapies are generally allowed — confirm with trial site)
- You have a history of non-infectious lung inflammation (pneumonitis) or scarring lung disease that needed steroid treatment, or you currently have this condition
- You have previously had a stem cell or solid organ transplant
- You have not fully recovered from a major surgery, or you still have complications from a recent surgery
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.
Contact this trial
Principal Investigator: Medical Director, Merck Sharp & Dohme LLC
Phone: 1-888-577-8839
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
Where this trial is recruiting
Primary endpoints
Percentage of Participants with a Dose Limiting Toxicity (DLT); Percentage of Participants who Experience at Least One Adverse Event (AE); Percentage of Participants who Discontinue Study Intervention Due to an AE; Objective Response Rate (ORR) per Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 as assessed by Blinded Independent Central Review (BICR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.