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Study of Brentuximab Vedotin And Bevacizumab In Refractory CD-30 Positive Germ Cell Tumors - Trial NCT02988843

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.

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NCT02988843
Phase 2
Terminated
drug
Trial Details
ClinicalTrials.gov โ€ข NCT02988843
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Study of Brentuximab Vedotin And Bevacizumab In Refractory CD-30 Positive Germ Cell Tumors
Phase II Study of Brentuximab Vedotin and Bevacizumab in Men With Refractory CD-30 Positive Germ Cell Tumors

Study Focus

Germ Cell Tumor

Brentuximab Vedotin

Interventional

drug

Sponsor & Location

Masonic Cancer Center, University of Minnesota

Minneapolis, United States of America

Timeline & Enrollment

Phase 2

Mar 29, 2017

Dec 15, 2019

1 participants

Primary Outcome

Disease Response Rate as Defined by the RECIST 1.1 Criteria, Integrated With Tumor Marker Response.

Summary

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.

ICD-10 Classifications

Malignant neoplasms
Malignant neoplasm: Jejunum
Malignant neoplasm: Prepuce
Malignant neoplasm: Female genital organ, unspecified
Malignant neoplasm: Vulva, unspecified

Data Source

ClinicalTrials.gov

NCT02988843

Non-Device Trial