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Spots Global Cancer Trial Database for Temsirolimus in Myelodysplastic Syndrome (MDS)

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Trial Identification

Brief Title: Temsirolimus in Myelodysplastic Syndrome (MDS)

Official Title: Treatment of MDS Patients With Single Agent Temsirolimus - a Pilot Study

Study ID: NCT01111448

Interventions

Temsirolimus

Study Description

Brief Summary: The goal of this Pilot-study is to evaluate the response of unselected MDS patients to temsirolimus a drug approved for the treatment of renal cell cancer. It is planned to give temsirolimus at a weekly dose of 25 mg as intravenous infusion for a maximum duration of 12 months. Regular bone marrow biopsies are planned for controlling MDS response.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Klinikum Chemnitz Klinik fĂźr Innere Medizin III, Chemnitz, , Germany

Universitätsklinikum C. G. Carus der TU Dresden, Dresden, , Germany

Universitätsklinikum Dßsseldorf Klinik fßr Hämatologie, Onkologie und Klin. Immunologie, Dßsseldorf, , Germany

Universitätsmedizin GÜttingen Georg-August-Universität Abteilung Hämatologie und Onkologie, Goettingen, , Germany

Universitätsklinikum Leipzig AÜR, Leipzig, , Germany

Forschungsgesellschaft mbH, Leipzig, , Germany

Klinikum Mannheim GmbH III. Medizinische Universitätsklinik -SP Hämatologie/Onkologie, Mannheim, , Germany

Contact Details

Name: Uwe Platzbecker, MD, PhD

Affiliation: Medizinische Klinik I, Universitätsklinikum Carl-Gustav-Carus, Dresden, Germany

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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