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2024-516063-89-00Active, not recruitingPhase 3

Phase 3 study of RMC-6236 in patients with previously treated metastatic PDAC

RASolute 302: A Phase 3 Multicenter, Open-label, Randomized Study of RMC-6236 versus Investigator’s Choice of Standard of Care Therapy in Patients with Previously Treated Metastatic Pancreatic Ductal Adenocarcinoma (PDAC)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 29 Oct 2026

Next steps

Brief summary (registry, in English)

In the RAS G-12 population (referred to as RAS G12 population): To compare the effect of treatment with RMC-6236 versus Investigator’s choice of standard therapy on: PFS OS

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
136 (estimated)
First submitted
13 Sept 2024
Start date
10 Apr 2025
Lead sponsor
Revolution Medicines Inc.
EU CT number
2024-516063-89-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 136
  • 16 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior therapy with any direct RAS-targeted therapy (eg, degraders and/or inhibitors).
  • Major surgery within 4 weeks prior to randomization.

Other illness

  • History of or known central nervous system metastatic disease.
  • Any conditions that may affect the ability to take or absorb study treatment.

Other

  • Patient is unable or unwilling to comply with all protocol-required study visits or procedures.

Who the study is looking for

  • At least 18 years of age and has provided informed consent. Follow local regulatory requirements if the legal age of consent for study participation is >18 years old.
  • ECOG performance status 0 or 1.
  • Histologically or cytologically confirmed PDAC with metastatic disease
  • Measurable disease per RECIST 1.1
  • Adequate organ function (bone marrow, liver, kidney, coagulation)
  • One prior line of systemic therapy in the metastatic setting.
  • Documented RAS mutation status, either mutant or wild-type. RAS mutations are defined as nonsynonymous mutations in KRAS, NRAS, or HRAS at codons 12, 13, or 61 (G12, G13, or Q61).
  • Able to take oral medications

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (16)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Charite Universitaetsmedizin Berlin KöRBerlinGermanyActive, not recruiting
Universitaetsklinikum Heidelberg AöRHeidelbergGermanyActive, not recruiting
Klinikum der Universitaet Muenchen AöRMunichGermanyActive, not recruiting
Universitaetsklinikum Ulm AoRUlmGermanyActive, not recruiting
Hospital Universitari Vall d'HebronBarcelonaSpainActive, not recruiting
Hospital Universitario 12 de OctubreMadridSpainActive, not recruiting
Clínica Universidad de navarraPamplonaSpainActive, not recruiting
Hospital Clinico Universitario de ValenciaValenciaSpainActive, not recruiting
Institut Paoli-CalmettesMarseilleFranceActive, not recruiting
Centre De Lutte Contre Le Cancer Eugene MarquisRennes CedexFranceActive, not recruiting
Institut Gustave RoussyVillejuifFranceActive, not recruiting
Hopital Paul BrousseVillejuif CedexFranceActive, not recruiting
Istituto Europeo di Oncologia s.r.lMilanItalyActive, not recruiting
Fondazione IRCCS - Istituto Nazionale dei TumoriMilanItalyActive, not recruiting
Istituto Oncologico VenetoPadovaItalyActive, not recruiting
Azienda Ospedaliero Universitaria PisanaPisaItalyActive, not recruiting

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This page is information, not medical advice. Discuss any trial with your doctor.