RecruitingPhase IEN originalColorectal cancerMetastatic / advanced

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

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This phase I trial tests the safety, side effects, and best dose of ZEN003694 in combination with the usual treatment with capecitabine in treating patients with cancer that has spread from where it first started (primary site) to other places in the body (metastatic) or cannot be removed by surgery (unresectable) and that it has progressed on previous standard treatment. ZEN003694 is an inhibitor of a family of proteins called the bromodomain and extra-terminal (BET). It may prevent the growth of tumor cells that over produce BET protein. Capecitabine is in a class of medications called antimetabolites. It is taken up by cancer cells and breaks down into fluorouracil, a substance that kills cancer cells. Giving ZEN003694 in combination with capecitabine may be safe in treating patients with metastatic or unresectable solid tumors.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Rak, który się rozprzestrzenił lub nie można go usunąć operacyjnie i który nie zareagował na standardowe leczenie (w tym 5-FU lub kapecytabinę).
  • Pacjenci z rakiem jelita grubego mogą zostać poproszeni o wykonanie biopsji przed rozpoczęciem leczenia.
  • Rak, który można zmierzyć w badaniach obrazowych.
  • Wiek powyżej 18 lat.
  • Ogólny stan zdrowia pozwalający na udział w badaniu (odpowiadający ocenie 0-2 w skali ECOG).
  • Dostępna tkanka guza z poprzednich badań do analizy molekularnej.
  • Zakończenie wcześniejszego leczenia systemowego co najmniej 2 tygodnie lub 5 okresów półtrwania leku przed rozpoczęciem badania.
  • Prawidłowe wyniki badań krwi (liczba neutrofilów, płytki krwi) i parametrów wątrobowych oraz nerkowych.

✗ Disqualifies

  • Pacjenci poniżej 18 roku życia.
  • Pacjenci z chorobami współistniejącymi, które mogą wpływać na bezpieczeństwo lub skuteczność leczenia (niektóre choroby wątroby, nerek).
  • Pacjenci z aktywnym zakażeniem wirusem zapalenia wątroby typu B, które nie jest kontrolowane.
  • Pacjenci, którzy stosowali inne leki mogące wchodzić w interakcje z lekami badanymi.

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
July 9, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (22)

UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care

Irvine, United States

UC Irvine Health/Chao Family Comprehensive Cancer Center

Orange, United States

UF Health Cancer Institute - Gainesville

Gainesville, United States

Memorial Hospital East

Shiloh, United States

University of Kansas Clinical Research Center

Fairway, United States

University of Kansas Cancer Center

Kansas City, United States

University of Kansas Hospital-Westwood Cancer Center

Westwood, United States

Siteman Cancer Center at Saint Peters Hospital

City of Saint Peters, United States

Siteman Cancer Center at West County Hospital

Creve Coeur, United States

Washington University School of Medicine

St Louis, United States

Siteman Cancer Center-South County

St Louis, United States

Siteman Cancer Center at Christian Hospital

St Louis, United States

NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center

New York, United States

Montefiore Medical Center-Einstein Campus

The Bronx, United States

Montefiore Medical Center-Weiler Hospital

The Bronx, United States

Montefiore Medical Center - Moses Campus

The Bronx, United States

University of Cincinnati Cancer Center-UC Medical Center

Cincinnati, United States

University of Cincinnati Cancer Center-West Chester

West Chester, United States

University of Oklahoma Health Sciences Center

Oklahoma City, United States

University of Pittsburgh Cancer Institute (UPCI)

Pittsburgh, United States

Vanderbilt Breast Center at One Hundred Oaks

Nashville, United States

Vanderbilt University/Ingram Cancer Center

Nashville, United States

Trial contact

Site Public Contact

Fa-Chyi Lee

PRINCIPAL_INVESTIGATOR

Thomas J. George

PRINCIPAL_INVESTIGATOR

Joaquina C. Baranda

PRINCIPAL_INVESTIGATOR

Chaoyuan Kuang

PRINCIPAL_INVESTIGATOR

Davendra P. Sohal

PRINCIPAL_INVESTIGATOR

Susanna V. Ulahannan

PRINCIPAL_INVESTIGATOR

Site Public Contact

Anwaar Saeed

PRINCIPAL_INVESTIGATOR

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/8/2026.

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