A Study of Aplidin (Plitidepsin) 3 h iv in Subjects With Relapsing or Refractory Multiple Myeloma
This is a phase II study to determine the efficacy following treatment with Aplidin® 5
mg/m2, given as a 3 hours intravenous infusion every 2 weeks, in patients with relapsed or
refractory multiple myeloma (MM).
Clinical Study of Plitidepsin (Aplidin®) in Combination With Cytarabine in Patients With Relapsed/Refractory Leukemia
Phase 1/Phase 2
This is a Phase I/II study to determine the safety, tolerability and to identify the MTD and
DLT of Plitidepsin in combination with a fixed dose of Cytarabine in patients with
relapsed/refractory leukemia and to determine the response rate of the combination of
Plitidepsin with Cytarabine in patients with relapsed/refractory AML treated at the MTD.
A Study of Aplidin ( Plitidepsin) in Subjects With Advanced Prostate Cancer
This is a study to test the safety and efficacy of an investigational chemotherapy agent in
patients with advanced prostate cancer. Subjects who meet all entry criteria and have signed
the informed consent will be enrolled in the study. Participants will be required to attend
regular clinic visits to receive study medication and have their status monitored. A
detailed explanation can be provided by the investigator conducting the study.
Study of Plitidepsin in Combination With Sorafenib or Gemcitabine in Patients With Advanced Solid Tumors or Lymphomas
Phase I Multicenter, Open-label, Clinical and Pharmacokinetic Study of Plitidepsin in
Combination with Sorafenib or Gemcitabine in Patients with Advanced Solid Tumors or
Lymphomas to determine the maximum tolerated dose (MTD) and the recommended dose (RD) of
plitidepsin in combination with sorafenib or gemcitabine in patients with advanced solid
tumors or lymphomas.
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