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Spots Global Cancer Trial Database for END-1: First Line Chemotherapy for Advanced or Recurrent Endometrial Carcinoma With Carboplatin and Liposomal Doxorubicin

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Trial Identification

Brief Title: END-1: First Line Chemotherapy for Advanced or Recurrent Endometrial Carcinoma With Carboplatin and Liposomal Doxorubicin

Official Title: Phase II Multicentered Study of First-Line Chemotherapy for Advanced or Recurrent Endometrial Carcinoma With the Combination of Carboplatin and Liposomal Doxorubicin

Study ID: NCT00401635

Study Description

Brief Summary: The purpose of this study is to evaluate activity and toxicity of the combination of carboplatin and liposomal doxorubicin as first-line chemotherapy of patients with advanced or recurrent endometrial carcinoma.

Detailed Description: Treatment is planned with carboplatin AUC 5 given IV on day 1 and liposomal doxorubicin 40 mg/m2 given IV on day 1, with treatment repeated every 28 days. Delays in treatment administration and dose reductions have been planned according to toxicity.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Ospedale Fatebenefratelli, U.O. di Oncologia, Benevento, BN, Italy

Ospedale Pierantoni, Divisione di Oncologia Medica, Forli', FO, Italy

Istituto Nazionale dei Tumori , Divisione di Oncologia Medica B, Napoli, , Italy

Ospedale S. Giovanni Calibita Fatebenefratelli, Roma, , Italy

Contact Details

Name: Sandro Pignata, M.D., Ph.D

Affiliation: National Cancer Institute, Naples

Role: PRINCIPAL_INVESTIGATOR

Name: Francesco Perrone, M.D., Ph.D

Affiliation: National Cancer Institute, Naples

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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