Drug: eltrombopag olamine Given PO Other Names: Promacta SB 497115 SB-497115 SB497115 | Aplastic Anemia and MDS International Foundation

Clinical Trial: NCT01943851

Drug: eltrombopag olamine Given PO Other Names: Promacta SB 497115 SB-497115 SB497115
For more details on this clinical trial, including contact information, please see this trial’s listing on clinicaltrials.gov:

This is an open-label repeat dose, multicenter, 2-part study to determine the maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) for GSK525762 given once-daily (OD) orally and twice daily (BID) orally. Part 1 of the study is a dose escalation phase to select the recommended Part 2 dose (RP2D) based on the safety, PK, and PD profiles observed after oral administration of GSK525762. Eligible subjects with relapsed refractory hematological malignancies will be enrolled in the OD and/or BID dosing cohorts until a MTD is established. Subjects may continue treatment in the study until disease progression, unacceptable toxicity, or withdrawal of consent. Part 2 will explore clinical activity at the MTD or RP2D; separate expansion cohorts will be planned for acute myeloid leukemia (AML), non-Hodgkin's Lymphoma (NHL, including an exploratory sub-cohort of subjects with myc and B-Cell Leukemia (BCL)2 and/or BCL6 rearrangements/overexpression [double- and triple-hit lymphoma]), and multiple myeloma (MM). This is the first study of this agent to be conducted in subjects with these relapsed and/or refractory hematological malignancies for which no standard therapies are anticipated to result in a durable remission.

Study Date: 
Thu, 05/01/2014 to Sat, 07/01/2017
Bone Marrow Disease(s): 
myelodysplastic syndromes (MDS)
Drug: GSK525762 GSK525762 1 mg, 10 mg and 30 mg will be supplied as white to off-white, round, biconvex tablets with no markings. GSK525762 will be administered with 240 milliliter (mL) water.