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Be Part of Research - Trial Details - A Pivotal Bioequivalence Study of DOXIL/CAELYX (Doxorubicin HCL) in Patients With Advanced or Refractory Solid Malignancies Including Patients With Ovarian Cancer

A Pivotal Bioequivalence Study of DOXIL/CAELYX (Doxorubicin HCL) in Patients With Advanced or Refractory Solid Malignancies Including Patients With Ovarian Cancer

Completed

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Neoplasms
Ovarian Neoplasms
Carcinoma, Ovarian Epithelial
Breast Neoplasms


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of this study is to support the qualification of a replacement manufacturing site for DOXIL/CAELYX (doxorubicin HCL).

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

May 2013 Dec 2014

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Cycle 1 = Treatment A, Cycle 2 = Treatment B

Intervention Arm Group : Treatment A: DOXIL/CAELYX (doxorubicin);Treatment B: DOXIL/CAELYX (doxorubicin);

Intervention Type : DRUG
Intervention Description : Cycle 1 = Treatment B, Cycle 2 = Treatment A

Intervention Arm Group : Treatment A: DOXIL/CAELYX (doxorubicin);Treatment B: DOXIL/CAELYX (doxorubicin);



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • London


The study is sponsored by Janssen Research & Development, LLC




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Read full details for Trial ID: NCT01815294
Last updated 03 December 2015

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