Study of ICP-105 in Solid Tumors Patients

Status Completed

Clinical Trial Summary

Open-label, non-randomized, Phase I, dose-escalating, first-in-man study.

Clinical Trial Description

The study consisted of a screening period, a treatment period with repeated 28-day treatment cycles (duration treatment with ICP-105), and a follow-up period (within 30 days of the last dose and post-treatment follow-up 30 days after the last visit). The recruited patients receive a single dose on day 1, then after a 3-day washout period, multiple dosing will be initiated following dose-escalation schedule. The dose-limiting toxicity (DLT) assessment period consisted of Cycle 0 (single dose and washout period) and Cycle 1 (28-day cycle). ;

Study Design

Related Conditions & MeSH terms

Solid Tumor

Clinical Trial Details

NCT number	NCT03642834
Study type	Interventional
Source	Beijing InnoCare Pharma Tech Co., Ltd.
Contact
Status	Completed
Phase	Phase 1
Start date	September 21, 2018
Completion date	March 1, 2021

View Details

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