🇺🇸 FDA
Pipeline program

A multicentric, open-label, non-randomized study to evaluate the pharmacokinetic, safety and tolerability of ITF2357 given as an oral single 50 mg dose in participants with chronic hepatic impairment relative to matched participants with normal hepatic function.

ITF2357-60

Phase 1 other active

Quick answer

A multicentric, open-label, non-randomized study to evaluate the pharmacokinetic, safety and tolerability of ITF2357 given as an oral single 50 mg dose in participants with chronic hepatic impairment relative to matched participants with normal hepatic function. for Participants with normal hepatic function, Participants with moderate HI, Participants with mild HI is a Phase 1 program (other) at Italfarmaco S.p.A. with 1 ClinicalTrials.gov record(s).

Program details

Company
Italfarmaco S.p.A.
Indication
Participants with normal hepatic function, Participants with moderate HI, Participants with mild HI
Phase
Phase 1
Modality
other
Status
active

Clinical trials