drugset / Trial / NCT03854110

Trial to Evaluate Safety and Tolerability of GP-2250 in Combination With Gemcitabine

NCT03854110 ↗

Phase 1 Active not recruiting 64 enrolled Geistlich Pharma AG Translational Drug Development · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1 first in human, dose escalation trial of GP-2250 administered in combination with gemcitabine in subjects with advanced pancreatic cancer previously treated with 5-fluorouracil-based chemotherapy. Prior radiosensitization with gemcitabine, the use of 5-fluorouracil, FOLFIRINOX or Nab-paclitaxel/gemcitabine in the neoadjuvant setting, and prior pancreaticoduodenectomy (Whipple procedure) is allowed. If prior treatment with gemcitabine was at therapeutic doses, a minimum of 3 months must have elapsed since the end of such treatment. As a precursor to 5-FU use of capecitabine-based chemotherapy is also permitted.

Timeline

Start
2019-01-14
Primary completion
2026-06-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject MISETIONAMIDE Small molecule 250 mg Intravenous
Subject MISETIONAMIDE Small molecule 30 g Intravenous
Background Gemcitabine Small molecule 1000 mg/m2 —