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CompletedNCT03508011

A Study of IMP4297 in Patients With Advanced Solid Tumors

A Phase I, Open-label, Dose-escalation Study of the Safety and Pharmacokinetics of IMP4297 in Patients With Advanced Solid Tumors

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
57 (actual)
Sponsor
Impact Therapeutics, Inc. · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This is a Phase I, first-in-human, open-label, dose-escalation study of IMP4297 administered orally once every day to patients with advanced solid tumors for whom standard therapy either does not exist or has proven to be ineffective or intolerable. Patients with advanced breast cancer, ovarian cancer or prostate cancer are preferred. There are two stages to this study: a dose-escalation stage and a dose-expansion stage.

Conditions

Interventions

TypeNameDescription
DRUGIMP4297The dose levels will be escalated following a modified 3+3 dose escalation scheme.

Timeline

Start date
2017-08-23
Primary completion
2020-12-16
Completion
2020-12-16
First posted
2018-04-25
Last updated
2021-03-30

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT03508011. Inclusion in this directory is not an endorsement.

A Study of IMP4297 in Patients With Advanced Solid Tumors (NCT03508011) · Clinical Trials Directory