drugset / Trial / NCT02106494
A Prospective, Multicenter, Study of APF530 (Granisetron) SC for Prevention of CINV in Patients Receiving HEC
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary study objective is to demonstrate the superiority of APF530 500 mg given subcutaneously (SC) compared with ondansetron 0.15 mg/kg given intravenously (IV) (up to a maximum of 16 mg) in the delayed-phase (\> 24-120 hours) complete response (CR) rate (defined as no emesis and no use of rescue medications) in subjects receiving highly emetogenic chemotherapy (HEC) as defined by the 2011 ASCO CINV guidelines
Timeline
- Start
- 2014-03
- Primary completion
- 2015-05
- Completion
- 2015-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Granisetron | Other / unclassified | 10 mg | Subcutaneous |
| Comparator | Ondansetron | Other / unclassified | 0.15 mg/kg | Intravenous |
| Background | Dexamethasone | Small molecule | 12 mg | Intravenous |
| Background | Fosaprepitant | Other / unclassified | 150 mg | Intravenous |