Pure Global

Phase II Study of Cisplatin Plus Epirubicin Salvage Chemo in Refractory Germ Cell Tumors - Trial NCT00198172

Access comprehensive clinical trial information for NCT00198172 through Pure Global AI's free database. This Phase 2 trial is sponsored by Indiana University School of Medicine and is currently Terminated. The study focuses on Germ Cell Tumor. Target enrollment is 37 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.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT00198172
Phase 2
Terminated
drug
Trial Details
ClinicalTrials.gov โ€ข NCT00198172
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Phase II Study of Cisplatin Plus Epirubicin Salvage Chemo in Refractory Germ Cell Tumors
Phase II Study of Cisplatin Plus Epirubicin Salvage Chemotherapy in Refractory Germ Cell Tumors

Study Focus

Germ Cell Tumor

Cisplatin plus Epirubicin

Interventional

drug

Sponsor & Location

Indiana University School of Medicine

Indiana University

Indianapolis, United States of America

Timeline & Enrollment

Phase 2

Oct 01, 2000

Mar 01, 2007

37 participants

Primary Outcome

To determine the feasibility and toxicity of combining epirubicin to fixed dose cisplatin

Summary

This study proposes to evaluate the combination of cisplatin plus epirubicin in patients with
 refractory germ cell tumor not amendable to cure with surgery or standard platinum salvage
 chemotherapy. This regimen will be used in eligible patients after progression on ECOG Study
 E39897.

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

NCT00198172

Non-Device Trial