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Study details
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A Study of PARP1 Selective Inhibitor, EIK1004 (IMP1707)

Eikon Therapeutics
NCT IDNCT06907043ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

130

Study length

about 3.7 years

Ages

18–89

Locations

6 sites in CO, FL, MA +2

What this study is about

This trial is testing a treatment called EIK1004 (IMP1707) in people with advanced solid tumors. The goal is to see if the treatment is safe and effective.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take EIK1004-001 (IMP1707-001)

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Number of Participants who experience a Dose-Limiting Toxicity (DLT), Number of participants with adverse events, treatment emergent adverse events or serious adverse events

Secondary: Objective Response (OR), Pharmacokinetic parameters of EIK1004 (IMP1707)