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Brief Title: Safety and Tolerability of Combined Treatment With Nilotinib and Ruxolitinib in CML and Ph+ ALL Patients
Official Title: A Phase Ib Single-arm, Open-label, Multicenter Study to Assess the Safety and Tolerability of Combined Treatment With Nilotinib 300mg BID and Ruxolitinib Increasing Dose in CML and Ph+ ALL Patients
Study ID: NCT02253277
Brief Summary: In this study it was the rationale to evaluate the safety and tolerability of the combined administration of nilotinib and increasing dose of ruxolitinib in patients with chronic myeloid leukemia and patients with Philadelphia positive acute lymphoblastic leukemia.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Novartis Investigative Site, Berlin, , Germany
Novartis Investigative Site, Frankfurt, , Germany
Novartis Investigative Site, Jena, , Germany
Novartis Investigative Site, Leipzig, , Germany
Name: Andreas Hochhaus, Prof. Dr. med.
Affiliation: Universitätsklinikum Jena
Role: PRINCIPAL_INVESTIGATOR