A Study of Avutometinib (VS-6766) + Defactinib (VS-6063) in Recurrent Low-Grade Serous Ovarian Cancer (RAMP 301)

NCT 06072781

Brief Summary

This study will assess the safety and efficacy of avutometinib (VS-6766) in combination with defactinib versus Investigator’s choice of treatments (ICT) in subjects with recurrent LGSOC who have progressed on a prior platinum-based therapy.

Intervention / Treatment

  • Drug: avutometinib
  • Drug: Defactinib
  • Drug: Pegylated liposomal doxorubicin
  • Drug: Paclitaxel
  • Drug: Letrozole
  • Drug: Anastrozole

Inclusion Criteria

Patients may be eligible for inclusion in the study if they meet the following criteria:

  1. Histologically proven LGSOC (ovarian, fallopian, peritoneal)
  2. Documented mutational status of KRAS by a validated tumor-tissue based diagnostic test.
  3. Suitable for treatment with at least one of the Investigator’s Choice of Treatments:pegylated liposomal doxorubicin, paclitaxel, letrozole, anastrozole.
  4. Progression or recurrence of LGSOC after at least one prior systemic therapy for metastatic disease.
  5. Measurable disease according to RECIST v1.1.
  6. An Eastern Cooperative Group (ECOG) performance status ≤ 1.
  7. Adequate organ function.
  8. Adequate recovery from toxicities related to prior treatments.
  9. For patients with reproductive potential, a negative pregnancy test must be confirmed and agreement to use highly effective method of contraceptive.
  10. Willingness to comply with the scheduled visits, treatment plan, laboratory tests and other study procedures.

Keep up with Rare Cancers Australia

Inside Rare is a monthly newsletter that shares the latest news, events and stories connecting the rare community.