WHO ICTRP trial

A PHASE II,MULTI-CENTER, OPEN LABEL STUDY OF ORAL LBH589 PLUS MELPHALAN…

EUCTR2007-007939-29-IT · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2007-007939-29-IT
Public title A PHASE II,MULTI-CENTER, OPEN LABEL STUDY OF ORAL LBH589 PLUS MELPHALAN, PREDNISONE AND THALIDOMIDE (LB-MPT)IN ADVANCED, REFRACTORY MULTIPLE MYELOMA PATIENTS. - LB-MPT
Scientific title A PHASE II,MULTI-CENTER, OPEN LABEL STUDY OF ORAL LBH589 PLUS MELPHALAN, PREDNISONE AND THALIDOMIDE (LB-MPT)IN ADVANCED, REFRACTORY MULTIPLE MYELOMA PATIENTS. - LB-MPT
Primary sponsor FONDAZIONE NEOPLASIE SANGUE ONLUS
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Italy
Conditions Patients with refractory or advanced Multiple Myeloma. MedDRA version: 9.1 Level: LLT Classification code 10051381 Term: Myeloma recurrence
Interventions Trade Name: Thalidomide Pharmaceutical Form: Capsule, hard INN or Proposed INN: Thalidomide Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 50- Pharmaceutical Form: Capsule, hard Concentration unit: mg…
Registration date Oct 14, 2008
Target size 42
Secondary IDs CLBH589BIT01T
Registry page clinicaltrialsregister.eu

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