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A Phase 1 Study of Brentuximab Vedotin Combined With ABVD for Hodgkin Lymphoma - NCT01060904-55905(Clinical Trial 493316)



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City:  Rochester
State:  
MN
Zip Code: 55905
Conditions: Disease, Hodgkin
Purpose: The purpose of this study is to assess the safety profile of brentuximab vedotin in combination with ABVD in treatment-naive Stage IIa or IIb-IV Hodgkin lymphoma. It is a phase 1, single-arm, open-label dose escalation study designed to define the MTD, PK, immunogenicity and anti-tumor activity of brentuximab vedotin in combination with frontline therapy.
Study summary:
Criteria: Inclusion Criteria: - Treatment-naive Hodgkin lymphoma, Stage IIa or IIb-IV - Measurable disease of at least 1.5 cm - ECOG performance status <3 Exclusion Criteria: - History of another primary malignancy that has not been in remission for at least 3 years - Known cerebral/meningeal disease
Study is available at: Mayo Clinic
Rochester, MN 55905
United States

Primary Contact:
Tami Simmons
Email: simmons.tamera@mayo.edu
Phone: 507-284-4740

Secondary Contact:
Terri Lowe
Email: clinicaltrials@seagen.com
Phone: 866-333-7436
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 23, 2011
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