Real-world Trial of Individualized Precision Oncology

Starting soon · Phase 2

Conditions studied: Metastatic Cancer, Unresectable Carcinoma

In brief

The goal of this clinical trial is to learn if drugs that are matched to tumor DNA mutations work to treat metastatic solid cancers in adults. The main questions it aims to answer are: Is tumor worsening delayed for a longer period of time if patients take drugs that match DNA mutations, compared to if they take standard of care drugs? Researchers will compare drugs matched to tumor DNA mutations to standard of care drugs to see if the matched drugs work better, and to see if tumor worsening can be delayed for longer the more DNA mutations the drugs target. Participants will: Take drugs matched to tumor DNA mutations or standard of care drugs based on the regular dosing schedule of the drugs. Visit the clinic every approximately 2 months for checkups and tumor imaging.

Key facts

Study ID

NCT07346209

Run by

University of California, San Diego

People needed

280

Starts

2026-06-01

Expected to finish

2031-09-01

Last updated by the study team

2026-04-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provision of signed and dated informed consent form.
• Stated willingness to comply with all study procedures and availability for the duration of the study.
• Aged at least 18 years.
• Metastatic or unresectable solid cancers (all) with a 2-year cancer-associated mortality of ≥ 50%, or immediate prior progression free survival < 4 months, or life expectancy between 6 and 16 months as determined at prescreening and/or enrollment due to cancer diagnosis.
• Previous treatment with up to 2 lines of cancer therapy before enrollment.
• Available results of tumor imaging performed within 4 weeks prior to randomization or eligible to obtain imaging as part of routine care. Note that patients are not eligible if their tumor imaging was performed more than 4 weeks before randomization, or if the imaging to be performed at screening is within 6 weeks of their previous imaging.
• Measurable disease by RECIST v 1.1 based on computed tomography, magnetic resonance imaging or positron emission tomography/computed tomography scan performed within 4 weeks prior to randomization.
• Case discussed by Molecular Tumor Board with consensus treatment recommendation(s).
• Presence of at least 1 tumor-derived molecular alteration/biomarker with a molecularly matched therapy option per Molecular Tumor Board recommendation.
• Molecular profile needs to be performed in tumor tissue or circulating tumor DNA collected in the 6 months before enrollment and analyzed by next generation sequencing, immunohistochemistry, and/or alternative technology in a Clinical Laboratory Improvement Amendments-accredited and College of American Pathologists-certified clinical laboratory.
• All prior pathology and molecular studies may be reviewed and considered by the Molecular Tumor Board.
• Molecularly matched therapy options are restricted to Food and Drug Administration-approved drugs.
• Eligible for at least 1 additional unmatched standard of care therapy.
• Eastern Cooperative Oncology Group performance status score of 0 or 1.
• At the time of the screening/baseline visit, patients must be off prior antibody therapy for at least 3 half-lives, and other anti-tumor agents for at least 5 half-lives, or total 3 weeks from the last day of treatment, whichever is shortest.
• Adequate hematologic, hepatic, and renal function, as specified below:
• Absolute Neutrophil Count ≥ 1.5 x 10\^9/L
• Hemoglobin ≥ 9 g/dL
• Platelets ≥ 50 x 10\^9/L
• Serum total bilirubin < 2.0 x upper limit of normal
• Aspartate aminotransferase and alanine aminotransferase ≤ 5 x upper limit of normal
• Serum creatinine ≤ 1.5 x upper limit of normal or calculated creatinine clearance ≥ 50ml/min based upon the Cockcroft-Gault Equation [CrCl = (140-age) * actual weight (in kg) * (0.85 if female) / (72 * Cr)].
• For participants able to become pregnant or cause a pregnancy: use of highly effective contraception during treatment with the study therapy and for 3 months afterwards.

You may not qualify if…

• Presence of very high tumor mutational burden as ≥ 20 mutations/megabase.
• Presence of a microsatellite instability-high as defined by the testing laboratory.
• Deficiency of mismatch repair genes: MLH1, MSH2, MSH6, or PMS2.
• Molecular Tumor Board treatment recommendation is a monotherapy with an immune checkpoint inhibitor.
• Molecular Tumor Board treatment recommendation is considered a standard of care regimen per NCCN guidelines (including treatments considered useful in certain circumstances).
• Example 1: Presence of BRAF V600E in lung cancer as the sole molecularly matched target is ineligible, given Food and Drug Administration approval of combination BRAFi/MEKi.
• Example 2: Presence of BRAF V600E and CDKN2A mutation in lung cancer is eligible, if the Molecular Tumor Board recommendation is the non-standard of care combination of BRAFi/MEKi + CDK4/6i
• Example 3: Presence of KRAS G12C in breast cancer is eligible as the use of KRAS inhibitors for this specific tumor type is not standard of care.
• Example 4: Presence of KRAS G12A mutation in colon cancer is eligible if the Molecular Tumor Board recommendation is for non-standard of care MEKi.
• Newly diagnosed symptomatic brain metastases requiring immediate treatment. Note that patients with asymptomatic or treated stable brain metastases not requiring steroids can be enrolled.
• Increase of Eastern Cooperative Oncology Group performance status of ≥ 1 point in the 30 days prior to enrollment.
• Pregnancy or lactation.
• Known allergic reactions to components of the therapy.
• Other conditions that preclude study participation at the discretion of the treating physician (e.g., organ or bone marrow dysfunction).
• Patient is in hospice care.
• Two oncologists disagree on prognosis or cancer resectability.

Where it is running

• University of California, San Diego — La Jolla, California, United States

Full record on ClinicalTrials.gov

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