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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 Oct 17, 2026, 1:59 AM 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 20, 2024 (Actual)
Primary completion
Jul 28, 2029 (Estimated)
Completion
Jul 28, 2029 (Estimated)
Last update posted
Jul 22, 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 22, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06157892 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →