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Title   Phase II Trial Testing the Antiemetic Efficacy of a Single-day Low Dose Aprepitant (or Fosaprepitant) Added to a 5-HT3 Receptor Antagonist Plus Dexamethasone in Patients Receiving Carboplatin
Disease/Condition   Oncology (Medical/Hematologic),Cancer
Description  

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Eligibility Criteria   Click here for eligibility requirements
Principal Investigator   Richard Gralla, MD
Contact Name   Karine Darbinyan
Contact Email   kadarbin@montefiore.org
Protocol Number   2015-5109
Inclusion/Notes   This Information was obtained from ClinicalTrials.gov
Status   Active/Enrolling
Adult Clinical Trial   Yes
Pediatric Clinical Trial   No
Sub-Specialty   Medical and Hematologic Oncology
Adult, Pediatric, Both   Adult