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A Phase 1/2 Study of VS-7375 in Patients With KRAS G12D-Mutated Solid Tumors
NCT07020221 · View on ClinicalTrials.gov ↗
Study Summary
This study will assess the safety and efficacy of VS-7375 alone and in combination in patients with advanced solid tumors harboring a KRAS G12D-mutation.
Conditions Studied
Interventions
- DRUG Cetuximab
- DRUG Gemcitabine
- DRUG VS-7375
- DRUG Carboplatin + Pemetrexed + Pembrolizumab
- DRUG Gemcitabine + Nab-paclitaxel
Study Locations (12)
California
- Cedars-Sinai Medical Center — Los Angeles
Maryland
- Johns Hopkins University — Baltimore
Massachusetts
- Massachusetts General Hospital — Boston
Michigan
- University of Michigan — Ann Arbor
Missouri
- Washington University School of Medicine — St Louis
New York
- Laura & Isaac Perlmutter Cancer Center at NYU Langone — New York
Pennsylvania
- Univ of Pennsylvania, Abramson Cancer Center — Philadelphia
Tennessee
- SCRI Oncology Partners — Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 295 participants |
| Start Date | 2025-06-24 |
| Est. Completion | 2028-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07020221
The ClinicalTrials.gov registry entry for NCT07020221 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 295 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Verastem, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 5 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 5 interventions — of which Cetuximab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07020221 reports 12 study locations spanning 12 distinct geographic areas — top geographies include California, Maryland, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07020221 about?
NCT07020221 is a clinical study titled "A Phase 1/2 Study of VS-7375 in Patients With KRAS G12D-Mutated Solid Tumors". This study will assess the safety and efficacy of VS-7375 alone and in combination in patients with advanced solid tumors harboring a KRAS G12D-mutation.
What is the current status of trial NCT07020221?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 295 participants. The study started on 2025-06-24. Estimated completion is 2028-12.
What conditions does trial NCT07020221 study?
This clinical trial studies the following conditions: Colorectal Cancer, Non Small Cell Lung Cancer, Pancreatic Ductal Adenocarcinoma, Solid Tumor, Adult, G12D Mutated KRAS. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07020221?
The interventions under investigation include: Cetuximab (DRUG), Gemcitabine (DRUG), VS-7375 (DRUG), Carboplatin + Pemetrexed + Pembrolizumab (DRUG), Gemcitabine + Nab-paclitaxel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07020221?
This trial is sponsored by Verastem, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07020221 being conducted?
This trial has 12 study locations across California, Maryland, Massachusetts, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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