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Spots Global Cancer Trial Database for Brentuximab Vedotin With Pembrolizumab in Metastatic Solid Tumors

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Brentuximab Vedotin With Pembrolizumab in Metastatic Solid Tumors

Official Title: A Phase 2 Study of Brentuximab Vedotin in Combination With Pembrolizumab in Subjects With Metastatic Solid Malignancies

Study ID: NCT04609566

Study Description

Brief Summary: This trial will find out whether brentuximab vedotin and pembrolizumab work together to treat different types of cancer. There will be several different types of cancer studied in the trial. The cancer must have spread to other parts of the body (metastatic). The study will also find out what side effects occur. A side effect is anything the treatment does besides treat cancer. This is a multi-cohort study.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Oncology Associates, PC - HOPE, Tucson, Arizona, United States

Highlands Oncology Group, Springdale, Arkansas, United States

cCARE - Northern, Fresno, California, United States

The Angeles Clinic and Research Institute, Los Angeles, California, United States

Cedars Sinai Medical Center / Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California, United States

California Cancer Associates for Research and Excellence Inc (cCARE), San Marcos, California, United States

University of Colorado Hospital / University of Colorado, Aurora, Colorado, United States

Rocky Mountain Cancer Centers - Aurora, Denver, Colorado, United States

Memorial Healthcare System, Hollywood, Florida, United States

Memorial Healthcare System, Pembroke Pines, Florida, United States

Affiliated Oncologists, LLC, Chicago Ridge, Illinois, United States

Northwestern University, Chicago, Illinois, United States

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States

University of Kansas Cancer Center, Kansas City, Kansas, United States

Norton Cancer Institute, Louisville, Kentucky, United States

Henry Ford Health System, Detroit, Michigan, United States

Minnesota Oncology Hematology P.A., Minneapolis, Minnesota, United States

University of Nebraska Medical Center, Omaha, Nebraska, United States

Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States

New York Oncology Hematology, P.C., Clifton Park, New York, United States

Oncology Hematology Care, Cincinnati, Ohio, United States

Toledo Clinic Cancer Center, Toledo, Ohio, United States

Willamette Valley Cancer Institute and Research Center, Eugene, Oregon, United States

Texas Oncology - Austin Central, Austin, Texas, United States

Texas Oncology - Baylor Sammons Cancer Center, Dallas, Texas, United States

Texas Oncology - Fort Worth 12th Avenue, Fort Worth, Texas, United States

Oncology Consultants, PA, Houston, Texas, United States

Inova Schar Cancer Institute, Fairfax, Virginia, United States

Virginia Oncology Associates, Norfolk, Virginia, United States

Virginia Commonwealth University Medical Center, Richmond, Virginia, United States

Oncology and Hematology Associates of Southwest Virginia, Roanoke, Virginia, United States

Fred Hutchinson Cancer Center / Seattle Cancer Care Alliance / University of Washington, Seattle, Washington, United States

University of Ottawa / Ottawa General Hospital, Ottawa, Ontario, Canada

Jewish General Hospital, Montreal, Quebec, Canada

McGill University Department of Oncology / McGill University Health Centre, Montreal, Quebec, Canada

Contact Details

Name: Medical Monitor

Affiliation: Seagen Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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