drugset / Trial / NCT05490888

Single and Multiple Dose Escalation of PHIN-214 in Child-Pugh A and B Liver Cirrhotics

NCT05490888 ↗

Phase 1 Recruiting 74 enrolled PharmaIN
Non-randomizedSequentialOpen-labelTreatment

Summary

This 2-part study will evaluate PHIN-214 given as a single one-time dose (Part 1) and in multiple doses (given as daily doses for 28-days) (in Part 2). Specifically, this study evaluates PHIN-214, to determine the safety, tolerability, and pharmacokinetic effects of PHIN-214, and to establish the maximum tolerated dose or optimal beneficial dose in patients with Child Pugh A and B Cirrhosis.

Timeline

Start
2022-01-03
Primary completion
2026-05-31
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject PHIN-214 Unknown — Subcutaneous