The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: Temsirolimus in Myelodysplastic Syndrome (MDS)
Official Title: Treatment of MDS Patients With Single Agent Temsirolimus - a Pilot Study
Study ID: NCT01111448
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:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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
Name: Uwe Platzbecker, MD, PhD
Affiliation: Medizinische Klinik I, Universitätsklinikum Carl-Gustav-Carus, Dresden, Germany
Role: PRINCIPAL_INVESTIGATOR