Testing the Combination of the Anti-cancer Drugs ZEN003694 (ZEN-3694) and Talazoparib in Patients With Advanced Solid Tumors, The ComBET Trial

Part of paid clinical trials in Duarte, California.

Sponsor
National Cancer Institute (NCI)
Study ID
NCT05327010
Phase
PHASE2
Status
Recruiting

Conditions

  • Advanced Malignant Solid Neoplasm
  • Metastatic Malignant Solid Neoplasm
  • Unresectable Malignant Solid Neoplasm

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • BET Bromodomain Inhibitor ZEN-3694 — DRUG
    Given PO
  • Biopsy Procedure — PROCEDURE
    Undergo tumor biopsy
  • Biospecimen Collection — PROCEDURE
    Undergo blood sample collection
  • Diagnostic Imaging Testing — PROCEDURE
    Undergo diagnostic imaging
  • Talazoparib — DRUG
    Given PO

Study Details

This phase II trial tests whether ZEN003694 (ZEN-3694) in combination with talazoparib works to shrink tumors in patients with solid tumors that are unlikely to be cured or controlled with treatment and that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Another aim of this study is to find out if, and how, patients' genes influence their response to this specific drug combination. For this part of the study, investigators will run tests using samples of patients' tumor tissue and blood that will be collected during the study. ZEN-3694 is an inhibitor of a family of proteins called the bromodomain and extra-terminal (BET). It may prevent the growth of tumor cells that overproduce BET protein. Talazoparib is an inhibitor of PARP, an enzyme that helps repair deoxyribonucleic acid (DNA) when it becomes damaged. Blocking PARP may help keep cancer cells from repairing their damaged DNA, causing them to die. PARP inhibitors are a type of targeted therapy. Genes are pieces of the DNA code that individuals inherit from their parents. Some genes work to protect against cancer by correcting damage that can occur in the DNA when cells divide. BRCA1 and BRCA2 are two examples of these types of genes, and they are called tumor-suppressor genes. For example, if a person has a mutation in a BRCA1/2 gene they have a greatly increased risk of developing breast and ovarian cancer because their cells may no longer be able to completely repair damaged DNA. It is the accumulation of DNA damage which causes a cell to change into a cancerous cell. Other genes are also involved in this process, and these are called DNA damage repair genes. The KRAS mutation is a change in a protein in normal cells. Normally KRAS serves as an information hub for signals in the cell that lead to cell growth, but when there is a mutation in KRAS it signals too much and cells grow without being told to, which causes cancer. Combination therapy with ZEN-3694 and talazoparib may be effective at slowing or stopping tumor growth in patients with advanced cancer.

Key Dates

Start date
Nov 14, 2022
Status verified
Jan 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2027

Study Design

Enrollment
88 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Treatment (ZEN-3694, talazoparib)
    Patients receive ZEN-3694 PO QD and talazoparib PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo diagnostic imaging, blood sample collection, and tumor biopsy throughout the study.

Primary Outcome Measure

Objective response rate (ORR) [ Time Frame: From initiation of treatment to first response ]

Locations (36)

FacilityCityStateZIPSite coordinators
City of Hope Comprehensive Cancer CenterDuarteCalifornia91010
Site Public Contact
800-826-4673
Jyoti Malhotra (PRINCIPAL_INVESTIGATOR)
City of Hope at Irvine LennarIrvineCalifornia92618
Site Public Contact
877-467-3411
Jyoti Malhotra (PRINCIPAL_INVESTIGATOR)
UC San Diego Moores Cancer CenterLa JollaCalifornia92093
Site Public Contact
858-822-5354
Rana R. McKay (PRINCIPAL_INVESTIGATOR)
Keck Medicine of USC KoreatownLos AngelesCalifornia90020-
Los Angeles General Medical CenterLos AngelesCalifornia90033-
USC / Norris Comprehensive Cancer CenterLos AngelesCalifornia90033-
USC Norris Oncology/Hematology-Newport BeachNewport BeachCalifornia92663-
University of California Davis Comprehensive Cancer CenterSacramentoCalifornia95817-
UC San Diego Medical Center - HillcrestSan DiegoCalifornia92103
Site Public Contact
Rana R. McKay (PRINCIPAL_INVESTIGATOR)
UCHealth University of Colorado HospitalAuroraColorado80045
Site Public Contact
720-848-0650
Bradley R. Corr (PRINCIPAL_INVESTIGATOR)
Yale UniversityNew HavenConnecticut06520-
Smilow Cancer Hospital Care Center-TrumbullTrumbullConnecticut06611-
UF Health Cancer Institute - GainesvilleGainesvilleFlorida32610-
Emory University Hospital/Winship Cancer InstituteAtlantaGeorgia30322
Site Public Contact
404-778-1868
Ticiana A. Leal (PRINCIPAL_INVESTIGATOR)
Northwestern UniversityChicagoIllinois60611
Site Public Contact
312-695-1301
Aparna Kalyan (PRINCIPAL_INVESTIGATOR)
University of Kansas Clinical Research CenterFairwayKansas66205
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Cancer CenterKansas CityKansas66160
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Cancer Center-Overland ParkOverland ParkKansas66210
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Hospital-Indian Creek CampusOverland ParkKansas66211
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Hospital-Westwood Cancer CenterWestwoodKansas66205
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kentucky/Markey Cancer CenterLexingtonKentucky40536
Site Public Contact
859-257-3379
Rachel W. Miller (PRINCIPAL_INVESTIGATOR)
Ochsner Medical Center JeffersonNew OrleansLouisiana70121
Site Public Contact
504-842-8084
Daniel Johnson (PRINCIPAL_INVESTIGATOR)
National Cancer Institute Developmental Therapeutics ClinicBethesdaMaryland20892
Site Public Contact
800-411-1222
A P. Chen (PRINCIPAL_INVESTIGATOR)
National Institutes of Health Clinical CenterBethesdaMaryland20892-
University of Kansas Cancer Center - NorthKansas CityMissouri64154
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Cancer Center - Lee's SummitLee's SummitMissouri64064
Site Public Contact
913-588-3671
Joaquina C. Baranda (PRINCIPAL_INVESTIGATOR)
University of Kansas Cancer Center at North Kansas City HospitalNorth Kansas CityMissouri64116-
UNC Lineberger Comprehensive Cancer CenterChapel HillNorth Carolina27599
Site Public Contact
877-668-0683
Shetal Patel (PRINCIPAL_INVESTIGATOR)
University of Pittsburgh Cancer Institute (UPCI)PittsburghPennsylvania15232
Site Public Contact
412-647-8073
Leonard J. Appleman (PRINCIPAL_INVESTIGATOR)
University of Texas at AustinAustinTexas78712-
University of Texas Medical BranchGalvestonTexas77555-0565
Site Public Contact
409-772-1950
Maurice Willis (PRINCIPAL_INVESTIGATOR)
M D Anderson Cancer CenterHoustonTexas77030
Site Public Contact
877-632-6789
Timothy A. Yap (PRINCIPAL_INVESTIGATOR)
University of Texas Health Science Center at San AntonioSan AntonioTexas78229
John Sarantopoulos
210-450-1785
John Sarantopoulos (PRINCIPAL_INVESTIGATOR)
Huntsman Cancer Institute/University of UtahSalt Lake CityUtah84112-
University of Virginia Cancer CenterCharlottesvilleVirginia22908
Site Public Contact
434-243-6303
Linda R. Duska (PRINCIPAL_INVESTIGATOR)
VCU Massey Comprehensive Cancer CenterRichmondVirginia23298
Site Public Contact
804-628-6430
Emily N. Kinsey (PRINCIPAL_INVESTIGATOR)

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