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Study of RAS(ON) Inhibitors in Patients With Gastrointestinal Solid Tumors

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NCT06445062 · readout in 269 d

Sponsored by Revolution Medicines, Inc. (industry) · RVMD — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
1,130estimated
Sites
32
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-05-24actualWhen the study began enrolling
Primary completion2027-05-15estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-07-15estimatedThe whole study's end, after follow-up
First posted2024-06-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Colorectal Cancer
  • CRC
  • Pancreatic Ductal Adenocarcinoma
  • PDAC
  • Gastrointestinal Cancer
  • Metastatic Pancreatic Ductal Adenocarcinoma

Interventions

  • Drug: RMC-6236
  • Drug: mFOLFOX6 regimen
  • Drug: bevacizumab
  • Drug: mFOLFIRINOX regimen
  • Drug: cetuximab
  • Drug: gemcitabine
  • Drug: nab-paclitaxel
  • Drug: RMC-9805

Primary outcomes

what the primary-completion date above is the date OF
Adverse events
measured Up to 3 years
Dose limiting toxicities
measured 28 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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