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Spots Global Cancer Trial Database for A Study of Brentuximab Vedotin With Hodgkin Lymphoma (HL) and CD30-expressing Peripheral T-cell Lymphoma (PTCL)

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: A Study of Brentuximab Vedotin With Hodgkin Lymphoma (HL) and CD30-expressing Peripheral T-cell Lymphoma (PTCL)

Official Title: A Phase 2 Open-label Study of Brentuximab Vedotin in Front-line Therapy of Hodgkin Lymphoma (HL) an dCD30-expressing Peripheral T-cell Lymphoma (PTCL) in Older Patients or Patients With Significant Comorbidities Ineligible for Standard Chemotherapy

Study ID: NCT01716806

Study Description

Brief Summary: This trial will study brentuximab vedotin to find out whether it is an effective treatment for Hodgkin lymphoma (HL) and peripheral T-cell lymphoma (PTCL). Participants in this study will be older or will have other conditions that make them unable to have standard chemotherapy treatment. The study will look at brentuximab vedotin alone and combined with other drugs.

Detailed Description: This study is designed to evaluate the efficacy and tolerability of brentuximab vedotin as monotherapy and in combination with other agents as frontline therapy. There are 6 parts of the study. The population to be studied includes treatment-naïve patients with classical Hodgkin lymphoma (HL) or treatment-naïve patients with CD30-expressing peripheral T-cell lymphoma (PTCL).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

University of South Alabama - Mitchell Cancer Institute, Mobile, Alabama, United States

Alaska Urological Institute, Anchorage, Alaska, United States

Banner MD Anderson Cancer Center, Gilbert, Arizona, United States

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

Arizona Cancer Center / University of Arizona, Tucson, Arizona, United States

Highlands Oncology Group, Springdale, Arkansas, United States

Providence St Joseph Medical Center, Burbank, California, United States

City of Hope National Medical Center, Duarte, California, United States

Wilshire Oncology Medical Group Inc., Pomona, California, United States

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

Florida Cancer Affiliates, Trinity, Florida, United States

IACT Health, Columbus, Georgia, United States

Georgia Cancer Specialists / Northside Hospital Cancer Institute, Sandy Springs, Georgia, United States

Rush University Medical Center, Chicago, Illinois, United States

Illinois Cancer Specialists / Advocate Lutheran General Hospital, Niles, Illinois, United States

American Oncology Networks LLC, Bethesda, Maryland, United States

Karmanos Cancer Institute / Wayne State University, Detroit, Michigan, United States

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

Nebraska Cancer Specialists, Omaha, Nebraska, United States

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

Morristown Medical Center/ Carol G. Simon Cancer Center, Morristown, New Jersey, United States

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, United States

New York Oncology Hematology, P.C., Albany, New York, United States

Columbia University Medical Center, New York, New York, United States

James P. Wilmot Cancer Center / University of Rochester Medical Center, Rochester, New York, United States

Oncology Hematology Care, Cincinnati, Ohio, United States

James Cancer Hospital / Ohio State University, Columbus, Ohio, United States

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

Northwest Cancer Specialists, P.C., Tigard, Oregon, United States

Prisma Health, Greenville, South Carolina, United States

Arlington Cancer Center, Arlington, Texas, United States

Texas Oncology - Bedford, Bedford, Texas, United States

Texas Oncology - Presbyterian Cancer Center Dallas, Dallas, Texas, United States

Texas Oncology - Denton South, Denton, Texas, United States

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

Houston Methodist Cancer Center, Houston, Texas, United States

MD Anderson Cancer Center / University of Texas, Houston, Texas, United States

Texas Oncology - Longview, Longview, Texas, United States

Texas Oncology - McAllen, McAllen, Texas, United States

Texas Oncology - Seton Williamson, Round Rock, Texas, United States

Virginia Cancer Specialists, PC, Fairfax, Virginia, United States

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

Oncology and Hematology Assoc of SW VA DBA Blue Ridge Cancer Care, Salem, Virginia, United States

Shenandoah Oncology P.C., Winchester, Virginia, United States

Benaroya Research Institute/Virginia Mason Medical Center, Seattle, Washington, United States

Swedish Cancer Institute, Seattle, Washington, United States

Wenatchee Valley Medical Center, Wenatchee, Washington, United States

Carbone Cancer Center / University of Wisconsin, Madison, Wisconsin, United States

University of Alberta / Cross Cancer Institute, Edmonton, Alberta, Canada

London Health Sciences Centre - Victoria Hospital, London, Ontario, Canada

CIUSSS de L'Est de l'lle de Montreal / installation Hopital Maisonneuve-Rosemont, Montreal, Quebec, Canada

Jewish General Hospital, Montreal, Quebec, Canada

Royal Victoria Hospital, McGill University Health Centre, Montreal, Quebec, Canada

Contact Details

Name: Robert Sims, MD

Affiliation: Seagen Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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