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Spots Global Cancer Trial Database for Addition of Vandetanib to Standard Therapy Pegliposomal Doxorubicin (PLD)

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Trial Identification

Brief Title: Addition of Vandetanib to Standard Therapy Pegliposomal Doxorubicin (PLD)

Official Title: Addition of Vandetanib to Standard Therapy (Pegliposomal Doxorubicin) in Patients With Recurrent Ovarian Cancer. A Multicentre Phase I / Randomized Phase II Study

Study ID: NCT00862836

Conditions

Ovarian Cancer

Interventions

Vandetanib

Study Description

Brief Summary: This multi-centre, non-randomized open phase I/randomized phase II study will be conducted in 70 patients (10 in phase I, 60 in phase II) with platinum-refractory recurrent epithelial cancer of the ovary, fallopian tube or peritoneum. A total of approximately 5 national centers will participate in phase I of the study. If the starting criteria for phase II of the study are met at the end of phase I, a total of approximately 20 national centers will participate in phase II of the study.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Research Site, Ulm, Baden-Württemberg, Germany

Research Site, Wiesbaden, Hessen, Germany

Research Site, Essen, Nordrhein-Westfalen, Germany

Research Site, Kiel, Schleswig-Holstein, Germany

Research Site, Berlin, , Germany

Contact Details

Name: Clinical Sciences & Operations

Affiliation: Sanofi

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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