drugset / Trial / NCT03674294
Aprepitant Triple Therapy for the Prevention of CINV in Nondrinking and Young Women Who Received Moderately Emetogenic Chemotherapy
RandomizedParallel-groupDouble-blindPrevention
Summary
The purpose of this study is to study whether adding Aprepitant to Palonosetron and dexamethasone can further prevent the incidence and severity of nausea and vomiting caused by FOLFIRI or FOLFOX chemotherapy regimen among gastrointestinal malignancy patients with high risk factors of chemotherapy-associated adverse events.
Timeline
- Start
- 2015-08-04
- Primary completion
- 2020-03-31
- Completion
- 2020-06-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Aprepitant | Other / unclassified | 80 mg | Oral |
| Subject | Dexamethasone | Small molecule | 6 mg | Oral |
| Subject | Dexamethasone | Small molecule | 12 mg | Oral |
| Background | Palonosetron | Other / unclassified | 0.25 mg | Intravenous |