Evidence Based Medicine on FHIR Implementation Guide, published by HL7 International / Clinical Decision Support. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot3 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/ebm/ and changes regularly. See the Directory of published versions
| Page standards status: Informative |
version: 3; Last updated: 2026-08-13 13:49:10+0000
Profile: StudyRegistryRecord
ArtifactPublicationStatus: Active
Artifact Author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
url: https://fevir.net/resources/ResearchStudy/583768
identifier: FEvIR Object Identifier/583768, ClinicalTrials.gov/NCT05327010 (use: official), NCI-2022-02915, Registry Identifier/NCI-2022-02915, NCI10486, Other Identifier/10486, Other Identifier/10486, U.S. NIH Grant/Contract/UM1CA186688, FEvIR Linking Identifier/NCT05327010 FHIR Transform
name: NCT05327010_FHIR_Transform
title: Testing the Combination of the Anti-cancer Drugs ZEN003694 (ZEN-3694) and Talazoparib in Patients With Advanced Solid Tumors, The ComBET Trial
| Type | Value |
| Scientific title | Phase 2 Trial of the Combination of the BET Inhibitor, ZEN003694 (ZEN-3694), and the PARP Inhibitor Talazoparib, in Patients With Molecularly-Selected Solid Tumors (ComBET) |
citeAs:
Testing the Combination of the Anti-cancer Drugs ZEN003694 (ZEN-3694) and Talazoparib in Patients With Advanced Solid Tumors, The ComBET Trial [Database Entry: FHIR ResearchStudy Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 583768. Revised 2026-08-13. Available at: https://fevir.net/resources/ResearchStudy/583768. Computable resource at: https://fevir.net/resources/ResearchStudy/583768#json.
relatesTo
type: Transforms
target: https://clinicaltrials.gov/api/v2/studies/NCT05327010?format=json
relatesTo
type: Transformed With
target: https://fevir.net/ctgovconvert
relatesTo
type: Supported With
relatesTo
type: Supported With
status: Active
purposeType: Treatment Study
phase: Phase 2
studyDesign: Design Masking: None (Open Label), Design Allocation: NA, Uncontrolled cohort design, interventional research
condition: Advanced Malignant Solid Neoplasm, Metastatic Malignant Solid Neoplasm, Unresectable Malignant Solid Neoplasm
descriptionSummary:
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.
description:
PRIMARY OBJECTIVE:
I. To evaluate clinical response to the combination of BET bromodomain inhibitor ZEN-3694 (ZEN003694 [ZEN-3694]) and talazoparib using objective response rate (ORR) = (complete response [CR] + partial response [PR]).
SECONDARY OBJECTIVES:
I. To confirm the safety and toxicity profile of the combination of ZEN003694 (ZEN-3694) and talazoparib.
II. To evaluate the clinical benefit rate (stable disease [SD] > 6 months [m]+CR+PR) and progression-free survival (PFS).
III. To assess the pharmacodynamics of the combination of ZEN003694 (ZEN-3694) and talazoparib using pre- and on-treatment tumor biopsies.
IV. To characterize pharmacodynamic changes of exploratory biomarkers to the combination of ZEN003694 (ZEN-3694) and talazoparib in pre- and on-treatment tumor biopsies.
V. To assess putative predictive biomarkers of response and resistance to the combination of ZEN003694 (ZEN-3694) and talazoparib.
OUTLINE:
Patients receive ZEN-3694 orally (PO) once daily (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.
After completion of study treatment, patients are followed up 30 days after administration of the last dose of study drug and then every 3 months for up to 2 years.
site:
classifier: IPDSharing: Yes, IPDSharingDescription: NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page., Does not include healthy volunteers, Includes female subjects, Includes male subjects, Minimum Age: 18 Years, Age Group: Adult, Age Group: Older Adult, Has Results: False, Oversight Classifier: oversightHasDmc False, Oversight Classifier: isFdaRegulatedDrug True, Oversight Classifier: isFdaRegulatedDevice False
associatedParty
name: National Cancer Institute (NCI)
role: Sponsor
classifier: NIH
associatedParty
name: National Cancer Institute (NCI)
role: Lead sponsor
classifier: NIH
associatedParty
name: Timothy A Yap
role: Principal investigator
party: University of Texas MD Anderson Cancer Center LAO
progressStatus
state: Recruiting
progressStatus
state: Registration submission
actual: true
period: 2022-04-13 --> (ongoing)
progressStatus
state: Registration submission Quality Check
actual: true
period: 2022-04-13 --> (ongoing)
progressStatus
state: Record Verification
actual: true
period: ?? --> 2026-07
progressStatus
state: Update submission
actual: true
period: ?? --> 2026-07-17
progressStatus
state: Registration posting
actual: true
period: 2022-04-14 --> (ongoing)
progressStatus
state: Primary outcome data collection
actual: false
period: ?? --> 2026-12-31
progressStatus
state: Update posting
actual: true
period: ?? --> 2026-07-20
progressStatus
state: Overall study
actual: true
period: 2022-11-14 --> (ongoing)
progressStatus
state: Overall study
actual: false
period: ?? --> 2027-12-31
| TargetNumber | Eligibility |
| 88 | NCT05327010 Eligibility Criteria |
| Eligibility | Name | Description |
| Treatment (ZEN-3694, talazoparib) | 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. |
objective
type: Primary
OutcomeMeasures
Name Type Description Endpoint Objective response rate (ORR) Primary Systemically assessed per Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1. ORR = complete response + partial response. Complete response is defined as the disappearance of all target or non-target lesions. Partial response is defined as at least a 30% decrease in the sum of the diameters of target or non-target lesions.
Objective response rate (ORR)
objective
type: Secondary
outcomeMeasure
name: Duration of response
type: Secondary
description:
Assessed using RECIST v1.1.
endpoint: Duration of response
outcomeMeasure
name: Clinical benefit rate (CBR)
type: Secondary
description:
Assessed by radiographic disease assessments per RECIST v1.1. CBR = overall response + stable disease > 6 months. Stable disease is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease.
endpoint: Clinical benefit rate (CBR)
outcomeMeasure
name: Progression-free survival
type: Secondary
description:
Assessed by radiographic disease assessments per RECIST v1.1.
endpoint: Progression-free survival
outcomeMeasure
name: Overall survival
type: Secondary
description:
Assessed by radiographic disease assessments per RECIST v1.1.
endpoint: Overall survival
outcomeMeasure
name: Incidence of adverse events
type: Secondary
description:
Incidence and severity of adverse events and serious adverse events as graded by National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0. Includes significant changes in laboratory parameters, electrocardiograms, and vital signs. Summarized by grade and type.
endpoint: Incidence of adverse events
objective
type: Exploratory
outcomeMeasure
name: Treatment-induced changes in phospho-protein signaling
type: Exploratory
description:
Reverse phase proteomic array in pre- and on-treatment tumor biopsy samples conducted to assess treatment-induced changes in phospho-protein signaling, to correlate with treatment response and progression, and to assess changes in the levels of cytotoxic T lymphocyte precursor.
endpoint: Treatment-induced changes in phospho-protein signaling
outcomeMeasure
name: Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response
type: Exploratory
description:
Whole exome sequencing conducted on pre-treatment biopsy and at progression to correlate SNV and CNV profiles with treatment response.
outcomeMeasure
name: Gene expression profiling
type: Exploratory
description:
Ribonucleic acid (RNA) sequencing conducted for gene expression profiling.
endpoint: Gene expression profiling
outcomeMeasure
name: Correlate mutation profiles with tumor sequencing
type: Exploratory
description:
Using circulating tumor deoxyribonucleic acid (ctDNA) for correlation.
outcomeMeasure
name: Correlate baseline mutations with treatment response
type: Exploratory
description:
Using ctDNA for correlation.
endpoint: Correlate baseline mutations with treatment response
outcomeMeasure
name: Correlate changes in ctDNA variant allele frequencies with response
type: Exploratory
description:
Using ctDNA for correlation.
endpoint: Correlate changes in ctDNA variant allele frequencies with response
outcomeMeasure
name: Assess emergent resistant mutations
type: Exploratory
description:
Includes BRCA reversion.
endpoint: Assess emergent resistant mutations
outcomeMeasure
name: Analysis of formalin-fixed paraffin-embedded and blood and blood samples
type: Exploratory
description:
DNA, RNA, and protein analysis conducted.
endpoint: Analysis of formalin-fixed paraffin-embedded and blood and blood samples
Generated Narrative: EvidenceVariable #NCT05327010-drug------bet-bromodomain-inhibitor-zen-3694
Profile: VariableDefinition
name: NCT05327010_drug______bet_bromodomain_inhibitor_zen_3694
title: BET Bromodomain Inhibitor ZEN-3694
status: Active
description:
Given PO
note: , , ,
suggested alternative name: BETi ZEN-3694
suggested alternative name: ZEN 3694
suggested alternative name: ZEN-3694
suggested alternative name: ZEN003694
handling: boolean variable
classifier: Intervention Type: DRUG
Generated Narrative: EvidenceVariable #NCT05327010-procedure------biopsy-procedure
Profile: VariableDefinition
name: NCT05327010_procedure______biopsy_procedure
title: Biopsy Procedure
status: Active
description:
Undergo tumor biopsy
note: , ,
suggested alternative name: Biopsy
suggested alternative name: BIOPSY_TYPE
suggested alternative name: Bx
handling: boolean variable
classifier: Intervention Type: PROCEDURE
Generated Narrative: EvidenceVariable #NCT05327010-procedure------biospecimen-collection
Profile: VariableDefinition
name: NCT05327010_procedure______biospecimen_collection
title: Biospecimen Collection
status: Active
description:
Undergo blood sample collection
note: , , ,
suggested alternative name: Biological Sample Collection
suggested alternative name: Biospecimen Collected
suggested alternative name: Sample Collection
suggested alternative name: Specimen Collection
handling: boolean variable
classifier: Intervention Type: PROCEDURE
Generated Narrative: EvidenceVariable #NCT05327010-procedure------diagnostic-imaging-testing
Profile: VariableDefinition
name: NCT05327010_procedure______diagnostic_imaging_testing
title: Diagnostic Imaging Testing
status: Active
description:
Undergo diagnostic imaging
note: ,
suggested alternative name: Diagnostic Imaging
suggested alternative name: Medical Imaging
handling: boolean variable
classifier: Intervention Type: PROCEDURE
Generated Narrative: EvidenceVariable #NCT05327010-drug------talazoparib
Profile: VariableDefinition
name: NCT05327010_drug______talazoparib
title: Talazoparib
status: Active
description:
Given PO
note: , ,
suggested alternative name: BMN 673
suggested alternative name: BMN-673
suggested alternative name: BMN673
handling: boolean variable
classifier: Intervention Type: DRUG
Exception parsing generated Narrative (see /tmp/liquid-abd29a78-3adc-4bd0-98a3-55438a30a85b.html): Error in template: Root element is not 'div'
Generated Narrative: ResearchStudy #NCT05327010-Location-0-ResearchStudy
Profile: ResearchStudySite
status: Active
site: City of Hope Comprehensive Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-0
City of Hope Comprehensive Cancer Center
Address: Duarte California 91010 United States Position: 34.13945, -117.97729 General contact:
- Site Public Contact
- ph: 800-826-4673
- becomingapatient@coh.org
Principal investigator:
- Irene M. Kang
Generated Narrative: ResearchStudy #NCT05327010-Location-1-ResearchStudy
Profile: ResearchStudySite
status: Active
site: City of Hope at Irvine Lennar
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-1
City of Hope at Irvine Lennar
Address: Irvine California 92618 United States Position: 33.66946, -117.82311 General contact:
- Site Public Contact
- ph: 877-467-3411
Principal investigator:
- Irene M. Kang
Generated Narrative: ResearchStudy #NCT05327010-Location-2-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UC San Diego Moores Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-2
UC San Diego Moores Cancer Center
Address: La Jolla California 92093 United States Position: 32.84727, -117.2742 General contact:
- Site Public Contact
- ph: 858-822-5354
- cancercto@ucsd.edu
Principal investigator:
- Rana R. McKay
Generated Narrative: ResearchStudy #NCT05327010-Location-3-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Keck Medicine of USC Koreatown
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-3
Keck Medicine of USC Koreatown
Address: Los Angeles California 90020 United States Position: 34.05223, -118.24368
Generated Narrative: ResearchStudy #NCT05327010-Location-4-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Los Angeles General Medical Center
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-4
Los Angeles General Medical Center
Address: Los Angeles California 90033 United States Position: 34.05223, -118.24368
Generated Narrative: ResearchStudy #NCT05327010-Location-5-ResearchStudy
Profile: ResearchStudySite
status: Active
site: USC / Norris Comprehensive Cancer Center
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-5
USC / Norris Comprehensive Cancer Center
Address: Los Angeles California 90033 United States Position: 34.05223, -118.24368
Generated Narrative: ResearchStudy #NCT05327010-Location-6-ResearchStudy
Profile: ResearchStudySite
status: Active
site: USC Norris Oncology/Hematology-Newport Beach
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-6
USC Norris Oncology/Hematology-Newport Beach
Address: Newport Beach California 92663 United States Position: 33.61891, -117.92895
Generated Narrative: ResearchStudy #NCT05327010-Location-7-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of California Davis Comprehensive Cancer Center
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-7
University of California Davis Comprehensive Cancer Center
Address: Sacramento California 95817 United States Position: 38.58157, -121.4944
Generated Narrative: ResearchStudy #NCT05327010-Location-8-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UC San Diego Medical Center - Hillcrest
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-8
UC San Diego Medical Center - Hillcrest
Address: San Diego California 92103 United States Position: 32.71571, -117.16472 General contact:
- Site Public Contact
- rhabbaba@health.ucsd.edu
Principal investigator:
- Rana R. McKay
Generated Narrative: ResearchStudy #NCT05327010-Location-9-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UCHealth University of Colorado Hospital
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-9
UCHealth University of Colorado Hospital
Address: Aurora Colorado 80045 United States Position: 39.72943, -104.83192
Generated Narrative: ResearchStudy #NCT05327010-Location-10-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Yale University
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-10
Yale University
Address: New Haven Connecticut 06520 United States Position: 41.30815, -72.92816
Generated Narrative: ResearchStudy #NCT05327010-Location-11-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Smilow Cancer Hospital Care Center-Trumbull
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-11
Smilow Cancer Hospital Care Center-Trumbull
Address: Trumbull Connecticut 06611 United States Position: 41.24287, -73.20067
Generated Narrative: ResearchStudy #NCT05327010-Location-12-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UF Health Cancer Institute - Gainesville
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-12
UF Health Cancer Institute - Gainesville
Address: Gainesville Florida 32610 United States Position: 29.65163, -82.32483
Generated Narrative: ResearchStudy #NCT05327010-Location-13-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Emory University Hospital/Winship Cancer Institute
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-13
Emory University Hospital/Winship Cancer Institute
Address: Atlanta Georgia 30322 United States Position: 33.749, -84.38798 General contact:
- Site Public Contact
- ph: 404-778-1868
Principal investigator:
- Ticiana A. Leal
Generated Narrative: ResearchStudy #NCT05327010-Location-14-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Northwestern University
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-14
Northwestern University
Address: Chicago Illinois 60611 United States Position: 41.85003, -87.65005 General contact:
- Site Public Contact
- ph: 312-695-1301
- cancer@northwestern.edu
Principal investigator:
- Aparna Kalyan
Generated Narrative: ResearchStudy #NCT05327010-Location-15-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Clinical Research Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-15
University of Kansas Clinical Research Center
Address: Fairway Kansas 66205 United States Position: 39.02223, -94.6319 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-16-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-16
University of Kansas Cancer Center
Address: Kansas City Kansas 66160 United States Position: 39.11417, -94.62746 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-17-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Cancer Center-Overland Park
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-17
University of Kansas Cancer Center-Overland Park
Address: Overland Park Kansas 66210 United States Position: 38.98223, -94.67079 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-18-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Hospital-Indian Creek Campus
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-18
University of Kansas Hospital-Indian Creek Campus
Address: Overland Park Kansas 66211 United States Position: 38.98223, -94.67079 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-19-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Hospital-Westwood Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-19
University of Kansas Hospital-Westwood Cancer Center
Address: Westwood Kansas 66205 United States Position: 39.04056, -94.6169 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-20-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kentucky/Markey Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-20
University of Kentucky/Markey Cancer Center
Address: Lexington Kentucky 40536 United States Position: 37.98869, -84.47772 General contact:
- Site Public Contact
- ph: 859-257-3379
Principal investigator:
- Rachel W. Miller
Generated Narrative: ResearchStudy #NCT05327010-Location-21-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Ochsner Medical Center Jefferson
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-21
Ochsner Medical Center Jefferson
Address: New Orleans Louisiana 70121 United States Position: 29.95465, -90.07507 General contact:
- Site Public Contact
- ph: 504-842-8084
- Elisemarie.curry@ochsner.org
Principal investigator:
- Daniel Johnson
Generated Narrative: ResearchStudy #NCT05327010-Location-22-ResearchStudy
Profile: ResearchStudySite
status: Active
site: National Cancer Institute Developmental Therapeutics Clinic
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-22
National Cancer Institute Developmental Therapeutics Clinic
Address: Bethesda Maryland 20892 United States Position: 38.98067, -77.10026 General contact:
- Site Public Contact
- ph: 800-411-1222
Principal investigator:
- A P. Chen
Generated Narrative: ResearchStudy #NCT05327010-Location-23-ResearchStudy
Profile: ResearchStudySite
status: Active
site: National Institutes of Health Clinical Center
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-23
National Institutes of Health Clinical Center
Address: Bethesda Maryland 20892 United States Position: 38.98067, -77.10026
Generated Narrative: ResearchStudy #NCT05327010-Location-24-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Cancer Center - North
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-24
University of Kansas Cancer Center - North
Address: Kansas City Missouri 64154 United States Position: 39.09973, -94.57857 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-25-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Cancer Center - Lee's Summit
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-25
University of Kansas Cancer Center - Lee's Summit
Address: Lee's Summit Missouri 64064 United States Position: 38.91084, -94.38217 General contact:
- Site Public Contact
- ph: 913-588-3671
- KUCC_Navigation@kumc.edu
Principal investigator:
- Joaquina C. Baranda
Generated Narrative: ResearchStudy #NCT05327010-Location-26-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Kansas Cancer Center at North Kansas City Hospital
ProgressStatuses
State Temporarily Closed to Accrual
Generated Narrative: Location #NCT05327010-Location-26
University of Kansas Cancer Center at North Kansas City Hospital
Address: North Kansas City Missouri 64116 United States Position: 39.13, -94.56218
Generated Narrative: ResearchStudy #NCT05327010-Location-27-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UNC Lineberger Comprehensive Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-27
UNC Lineberger Comprehensive Cancer Center
Address: Chapel Hill North Carolina 27599 United States Position: 35.9132, -79.05584 General contact:
- Site Public Contact
- ph: 877-668-0683
- cancerclinicaltrials@med.unc.edu
Principal investigator:
- Shetal Patel
Generated Narrative: ResearchStudy #NCT05327010-Location-28-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Pittsburgh Cancer Institute (UPCI)
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-28
University of Pittsburgh Cancer Institute (UPCI)
Address: Pittsburgh Pennsylvania 15232 United States Position: 40.44062, -79.99589 General contact:
- Site Public Contact
- ph: 412-647-8073
Principal investigator:
- Leonard J. Appleman
Generated Narrative: ResearchStudy #NCT05327010-Location-29-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Texas at Austin
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-29
University of Texas at Austin
Address: Austin Texas 78712 United States Position: 30.26715, -97.74306
Generated Narrative: ResearchStudy #NCT05327010-Location-30-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Texas Medical Branch
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-30
University of Texas Medical Branch
Address: Galveston Texas 77555-0565 United States Position: 29.30135, -94.7977 General contact:
- Site Public Contact
- ph: 409-772-1950
- clinical.research@utmb.edu
Principal investigator:
- Maurice Willis
Generated Narrative: ResearchStudy #NCT05327010-Location-31-ResearchStudy
Profile: ResearchStudySite
status: Active
site: UT MD Anderson Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-31
UT MD Anderson Cancer Center
Address: Houston Texas 77030 United States Position: 29.76328, -95.36327 General contact:
- Site Public Contact
- ph: 866-632-6789
- askmdanderson@mdanderson.org
Principal investigator:
- Timothy A. Yap
Generated Narrative: ResearchStudy #NCT05327010-Location-32-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Texas Health Science Center at San Antonio
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-32
University of Texas Health Science Center at San Antonio
Address: San Antonio Texas 78229 United States Position: 29.42412, -98.49363 General contact:
- John Sarantopoulos
- ph: 210-450-1785
- sarantopoulo@uthscsa.edu
Principal investigator:
- John Sarantopoulos
Generated Narrative: ResearchStudy #NCT05327010-Location-33-ResearchStudy
Profile: ResearchStudySite
status: Active
site: Huntsman Cancer Institute/University of Utah
ProgressStatuses
State Active, not recruiting
Generated Narrative: Location #NCT05327010-Location-33
Huntsman Cancer Institute/University of Utah
Address: Salt Lake City Utah 84112 United States Position: 40.76078, -111.89105
Generated Narrative: ResearchStudy #NCT05327010-Location-34-ResearchStudy
Profile: ResearchStudySite
status: Active
site: University of Virginia Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-34
University of Virginia Cancer Center
Address: Charlottesville Virginia 22908 United States Position: 38.02931, -78.47668 General contact:
- Site Public Contact
- ph: 434-243-6303
- uvacancertrials@hscmail.mcc.virginia.edu
Principal investigator:
- Linda R. Duska
Generated Narrative: ResearchStudy #NCT05327010-Location-35-ResearchStudy
Profile: ResearchStudySite
status: Active
site: VCU Massey Comprehensive Cancer Center
ProgressStatuses
State Recruiting
Generated Narrative: Location #NCT05327010-Location-35
VCU Massey Comprehensive Cancer Center
Address: Richmond Virginia 23298 United States Position: 37.55376, -77.46026 General contact:
- Site Public Contact
- ph: 804-628-6430
- CTOclinops@vcu.edu
Principal investigator:
- Emily N. Kinsey