A First-in-human Study of PARP1 Selective Inhibitor, IMP1734, in Participants With Advanced Solid Tumors

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A FIRST-IN-HUMAN, PHASE 1/2, OPEN-LABEL, MULTICENTER, DOSE-ESCALATION, DOSE-OPTIMIZATION, AND DOSE-EXPANSION STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS, AND ANTI-TUMOR ACTIVITY OF PARP1 SELECTIVE INHIBITOR, IMP1734, AS MONOTHERAPY AND IN COMBINATION IN PARTICIPANTS WITH ADVANCED SOLID TUMORS

Intervention/treatment:
EIK1003 (IMP1734)
Medical condition:
ADVANCED SOLID TUMORS
Protocol code:
EIK1003-001 (IMP1734-101)
Control number:
289728
Status:
Recruiting
Approved:
October 18, 2024
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT06253130
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 89 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Nicola Lynch
Role
CONTACT
Phone:
212-540-4923
Extension 104923
Sponsor
EIKON THERAPEUTICS, INC.

Locations

Alberta

Cross Cancer Institute
Edmonton, Alberta, T6G 1Z2
RECRUITING
Name
Noor Study Coordinator
Role
CONTACT
Name
Quincy Chu, MD
Role
PRINCIPAL_INVESTIGATOR

Ontario

Princess Margaret Cancer Centre-University Health Network
Toronto, Ontario, M5G 2M9
RECRUITING
Name
Riya Study Coordinator
Role
CONTACT
Name
Amit Oza, MD
Role
PRINCIPAL_INVESTIGATOR
Sunnybrook Research Institute
Toronto, Ontario, M4N 3M5
RECRUITING
Name
Donna Study Coordinator
Role
CONTACT
Name
Rossanna Pezo, MD
Role
PRINCIPAL_INVESTIGATOR
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