drugset / Trial / NCT05525247

A Phase 1/2, Open-label, Multicenter, Dose Escalation and Expansion Study of SLC-3010 Monotherapy and in Combination

NCT05525247

Phase 1/2 Terminated 27 enrolled Selecxine
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1/2, open-label, multicenter, dose escalation and expansion study, evaluating the safety, tolerability, pharmacokinetic, preliminary anti-tumor activity, and effects on pharmacodynamic markers following administration of SLC-3010 as monotherapy and in combination with gemcitabine, in patients with various advanced solid tumors.

Timeline

Start
2022-12-21
Primary completion
2025-08-26
Completion
2025-08-26

Drugs

EvaluationDrugModalityDoseRoute
Subject SLC-3010 Unknown Intravenous
Background Gemcitabine Small molecule 1000 mg/m2 Intravenous

Indications