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Clinical Trial Summary

The purpose of the meta-analysis was to explore the efficacy of eltrombopag versus placebo (standard of care)


Clinical Trial Description

Meta-analysis of three studies: Bussell 2007 & Bussell 2009 & RAISE (TRA102537). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01235988
Study type Observational
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date August 2009
Completion date October 2009

See also
  Status Clinical Trial Phase
Active, not recruiting NCT01440374 - A Three-part Study of Eltrombopag in Thrombocytopenic Subjects With Myelodysplastic Syndromes or Acute Myeloid Leukemia Phase 2
Completed NCT01957176 - A Rollover Study to Provide Continued Treatment With Eltrombopag Phase 4
Withdrawn NCT01055600 - Milk-only Lactation Study for Patients on Eltrombopag Phase 4
Completed NCT01147809 - Safety and Efficacy Study for Solid Tumor Patients Treated With Eltrombopag Phase 2
Terminated NCT02158936 - A Study of Eltrombopag or Placebo in Combination With Azacitidine in Subjects With International Prognostic Scoring System (IPSS) Intermediate-1, Intermediate-2 or High-risk Myelodysplastic Syndromes (MDS) Phase 3
Completed NCT00358540 - Dose Finding Study Of Oral Eltrombopag In Patients With Sarcoma Receiving Adriamycin And Ifosfamide Phase 1
Completed NCT00102726 - SB-497115 (Oral Thrombopoietin Receptor Agonist) Versus Placebo In Adult Cancer Patients Receiving Chemotherapy Phase 2
Completed NCT01236014 - Indirect Comparison Between Eltrombopag & Romiplostim N/A
Completed NCT01657552 - Eltrombopag/Boceprevir and Eltrombopag/Telaprevir Drug-Drug Interaction Study In Healthy Adult Subjects Phase 1