Study of Brentuximab Vedotin And Bevacizumab In Refractory CD-30 Positive Germ Cell Tumors
- Disease/Condition
- Germ Cell Tumor
- Drug/Device/Intervention
- Brentuximab Vedotin
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Masonic Cancer Center, University of Minnesota
- Location
- Minneapolis, United States of America
- Phase
- Phase 2
- Start date
- Mar 29, 2017
- End date
- Dec 15, 2019
- Enrollment
- 1 participants
Disease Response Rate as Defined by the RECIST 1.1 Criteria, Integrated With Tumor Marker Response.
This is a multi-center phase II study of brentuximab vedotin in combination with bevacizumab
 for the treatment of refractory CD-30+ germ cell tumors (GCT) after disease progression on
 imaging and/or tumor marker progression documented by serially rising alpha-fetoprotein (AFP)
 or beta human chorionic gonadotropin (bHCG) measured on at least 2 consecutive visits and
 determined by treating physician to be clinically significant. Patients unable to receive 2nd
 line of platinum-based chemotherapy due to toxicity or refusal would also be eligible.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT02988843
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT02988843 through Pure Global AI's free database. This Phase 2 trial is sponsored by Masonic Cancer Center, University of Minnesota and is currently Terminated. The study focuses on Germ Cell Tumor. Target enrollment is 1 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.