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Active, not recruiting Phase 2 Interventional

A Study of Disitamab Vedotin With Other Anticancer Drugs in Solid Tumors

ClinicalTrials.gov ID: NCT06157892

Public ClinicalTrials.gov record NCT06157892. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 11:08 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2 Open-Label Study of Disitamab Vedotin in Combination With Other Anticancer Therapies in Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This clinical trial is studying solid tumor cancers. A solid tumor is one that starts in part of your body like your lungs or liver instead of your blood. Once they've grown bigger in one spot or spread to other parts of the body, they're harder to treat. This is called advanced or metastatic cancer. Participants in this study must have breast cancer or gastric cancer. Participants must have tumors that have HER2 on them. This allows the cancer to grow more quickly or spread faster. There are few treatment options for patients with advanced or metastatic solid tumors that express HER2. This clinical trial uses an experimental drug called disitamab vedotin (DV). Disitamab vedotin is a type of antibody drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. This clinical trial uses a drug called tucatinib, which has been approved to treat cancer in the United States and some other countries. This drug is sold under the brand name TUKYSA®. This study will test how safe and how well DV with tucatinib works for participants with solid tumors. This study will also test what side effects happen when participants take these drugs. A side effect is anything a drug does to the body besides treating the disease.

Study identification

NCT ID
NCT06157892
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
54 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 19, 2024
Primary completion
Jul 27, 2029
Completion
Jul 27, 2029
Last update posted
Jul 21, 2026

2024 – 2029

United States locations

U.S. sites
77
U.S. states
18
U.S. cities
42
Facility City State ZIP Site status
Banner-University Medical Center Tucson Campus Tucson Arizona 85704
Banner-University Medical Center Tucson Campus Tucson Arizona 85719
The University of Arizona Cancer Center-North Campus Pharmacy, Attn: Kelly Myrdal Tucson Arizona 85719
University of Arizona Cancer Center - North Campus Tucson Arizona 85719
The University of Arizona Cancer Center-Main Tucson Arizona 85724
UC Irvine Health - Chao Family Comprehensive Cancer Center Orange California 92868
UC Irvine Medical Center Orange California 92868
University of California, San Francisco | HDFCCC - Hematopoietic Malignancies San Francisco California 94158
UCLA Department of Medicine - Hematology & Oncology Santa Monica California 90404
UCLA Hematology/Oncology - Parkside Santa Monica California 90404
Colorado West Healthcare System, dba Community Hospital Grand Junction Colorado 81505
Colorado West Healthcare, dba Grand Valley Oncology Grand Junction Colorado 81505
Georgetown University Medical Center Washington D.C. District of Columbia 20007
MedStar Georgetown University Hospital Washington D.C. District of Columbia 20007
Moffitt Cancer Center - International Plaza Tampa Florida 33607
H. Lee Moffitt Cancer Center and Research Institute Tampa Florida 33612
Moffitt Cancer Center - McKinley Campus Tampa Florida 33612
Moffitt McKinley Hospital Tampa Florida 33612
Moffitt Cancer Center at Wesley Chapel Wesley Chapel Florida 33544
Georgia Cancer Specialists - Athens Athens Georgia 30606
Georgia Cancer Specialists - Annex Atlanta Georgia 30341
Atlanta Cancer Care - Atlanta Atlanta Georgia 30342
Georgia Cancer Specialists-Northside Atlanta Georgia 30342
Northside Hospital, Inc.- Central Research Department Atlanta Georgia 30342
Northside Hospital Atlanta Georgia 30342
Georgia Cancer Specialists - Blairsville Blairsville Georgia 30512
Georgia Cancer Specialists - Canton Canton Georgia 30115
Atlanta Cancer Care - Cumming Cumming Georgia 30041
Georgia Cancer Specialists - Cumming Cumming Georgia 30041
Georgia Cancer Specialists - Decatur Decatur Georgia 30033
Suburban Hematology-Oncology Associates - Duluth Duluth Georgia 30096
Suburban Hematology-Oncology Associates- Lawrenceville Lawrenceville Georgia 30046
Georgia Cancer Specialists - Macon Macon Georgia 31217
Georgia Cancer Specialists - Marietta Marietta Georgia 30060
Memorial Hospital Shiloh Illinois 62269
Siteman Cancer Center - Shiloh Shiloh Illinois 62269
Massachusetts General Hospital. Boston Massachusetts 02114
Brigham and Women's Hospital Boston Massachusetts 02115
Dana Farber Cancer Institute Boston Massachusetts 02215
Dana Farber Cancer Institute- Chestnut Hill Newton Massachusetts 02459
Siteman Cancer Center - St Peters City of Saint Peters Missouri 63376
Siteman Cancer Center - West County Creve Coeur Missouri 63141
Siteman Cancer Center - North County Florissant Missouri 63031
Saint Luke's Cancer Institute LLC Kansas City Missouri 64111
Saint Luke's Hospital Investigational Pharmacy Kansas City Missouri 64111
Barnes-Jewish Hospital St Louis Missouri 63110
Washington University School of Medicine - Siteman Cancer Center St Louis Missouri 63110
Washington University School of Medicine St Louis Missouri 63110
Siteman Cancer Center - South County St Louis Missouri 63129
Renown Regional Medical Center Reno Nevada 89502
Memorial Sloan Kettering Cancer Center - Basking Ridge Basking Ridge New Jersey 07920
MSK Basking Ridge Basking Ridge New Jersey 07920
Memorial Sloan Kettering - Monmouth Middletown New Jersey 07748
MSK Monmouth. Middletown New Jersey 07748
Memorial Sloan Kettering - Bergen Montvale New Jersey 07645
MSK Bergen. Montvale New Jersey 07645
San Juan Oncology Associates Farmington New Mexico 87401
Memorial Sloan Kettering Cancer Center - Commack Commack New York 11725
MSK Commack. Commack New York 11725
Memorial Sloan Kettering - Westchester Harrison New York 10604
MSK Westchester. Harrison New York 10604
Investigational Drug Service Long Island City New York 11101
Memorial Sloan Kettering Cancer Center - Main Hospital New York New York 10065
Memorial Sloan Kettering Cancer Center New York New York 10065
Memorial Sloan Kettering- Nassau Uniondale New York 11553
MSK Nassau. Uniondale New York 11553
Zangmeister Cancer Center Columbus Ohio 43219
Saint Francis Hospital / Bon Secours - South Carolina Greenville South Carolina 29607
Sarah Cannon Research Institute - Pharmacy Nashville Tennessee 37203
SCRI Oncology Partners Nashville Tennessee 37203
Tennessee Oncology-Nashville/Sarah Cannon Research Institute Nashville Tennessee 37203
Providence Health and Services Washington and Montana Renton Washington 98057
Harborview Medical Center Seattle Washington 98104
Fred Hutchinson Cancer Center / Seattle Cancer Care Alliance / University of Washington Seattle Washington 98109
University of Washington Medical Center Seattle Washington 98195
University of Wisconsin Carbone Cancer Center - Eastpark Medical Center Madison Wisconsin 53718
Carbone Cancer Center / University of Wisconsin Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06157892, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06157892 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →