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Completed Phase 2 Interventional Results available

A Pivotal Open-Label Trial of Brentuximab Vedotin for Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT00848926

Public ClinicalTrials.gov record NCT00848926. 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 2, 2026, 3:40 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 Pivotal Study of SGN-35 in Treatment of Patients With Relapsed or Refractory Hodgkin Lymphoma (HL)

Brief summary

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

This is a single-arm, open-label, multicenter, pivotal clinical trial to evaluate the efficacy and safety of brentuximab vedotin (SGN-35) as a single agent in patients with relapsed or refractory Hodgkin lymphoma.

Study identification

NCT ID
NCT00848926
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Seagen Inc.
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 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
Jan 31, 2009
Primary completion
Jul 31, 2010
Completion
Apr 30, 2015
Last update posted
Mar 12, 2017

2009 – 2015

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294-3300
City of Hope National Medical Center Duarte California 91010-3000
University of California at Los Angeles Los Angeles California 90095
Stanford University Medical Center Palo Alto California 94305
Rocky Mountain Cancer Center Denver Colorado 80218
Georgetown University Washington D.C. District of Columbia 20007
University of Miami Miami Florida 33136
Loyola University Medical Center Cardinal Bernardin Cancer Center Maywood Illinois 60153
Karmanos Cancer Institute Detroit Michigan 48201
Mayo Clinic Rochester Rochester Minnesota 55905
Washington University School of Medicine St Louis Missouri 63110
Weill Cornell Medical College New York New York 10021
Memorial Sloan Kettering Cancer Center New York New York 10065
University of Rochester Medical Center Rochester New York 14642
Ohio State University Columbus Ohio 43210
Oregon Health & Science University Portland Oregon 97239
Baylor Sammons Cancer Center Dallas Texas 75246
University of Texas MD Anderson Cancer Center Houston Texas 77030-4009
University of Washington Seattle Washington 98109

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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00848926, 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 Mar 12, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00848926 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →