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Study details
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Testing the Addition of an Anti-Cancer Drug, ZEN003694, to the Usual Chemotherapy Treatment (Capecitabine) for Metastatic or Unresectable Cancers

National Cancer Institute (NCI)
NCT IDNCT05803382ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

30

Study length

about 2.6 years

Ages

18+

Locations

22 sites in CA, FL, IL +7

What this study is about

This trial is testing a treatment with ZEN003694 added to usual chemotherapy in patients whose cancer has spread or cannot be removed by surgery. The goal is to determine the safety and best dose of ZEN003694 when used together with capecitabine.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take BET Bromodomain Inhibitor ZEN-3694
  • 2.Take Capecitabine
  • 3.Undergo Biopsy Procedure
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

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

Drug classes

capecitabine

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Incidence of adverse events, Maximum tolerated dose (MTD), Recommended phase 2 dose (RP2D)

Secondary: Objective response rate (ORR), Pharmacodynamics (PD) of ZEN003694 (ZEN-3694) in combination with capecitabine, Pharmacokinetics (PK) of ZEN003694 (ZEN-3694) in combination with capecitabine, Progression free survival (PFS)

Procedures

biopsy, diagnostic, imaging

Body systems

Oncology