Metformin in Pseudomyxoma Peritonei Secondary to Appendiceal Mucinous Neoplasms

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of California, Irvine

About this trial

This is a pilot, open-label clinical trial determining the feasibility of metformin therapy in subjects with pseudomyxoma peritonei (PMP) secondary to appendiceal mucinous neoplasms (AMNs).

Eligibility criteria

Qualifiers

Patients with clinical diagnosis of pseudomyxoma peritonei (PMP) secondary to presumed appendiceal mucinous neoplasms (AMNs) with recurrent/refractory disease s/p cytoreductive surgery(CRS)/hyperthermic intraperitoneal chemotherapy (HIPEC), unresectable disease, or without planned CRS/HIPEC

Age ≥18 years

ECOG performance status ≤2

Disqualifiers

Patients with a clinical diagnosis of PMP secondary to presumed AMNs with resectable disease who are planned to undergo CRS/HIPEC

Patients currently taking metformin for another medical indication

Patients with a prior adverse event to administration of metformin

Trial design

Treatments tested in this trial

  • Metformin

Treatment groups

15 Participants
are divided into 1 treatment group