Standards message here

Benign Hematology Service

Infectious Disease

1

Disease Status and/or Stage Compromised GI function and at high risk for invasive fungal infection
Protocol Title A Phase 4 study of the Pharmacokinetics of Oral Posaconazole (SCH 56592) among Patients with Compromised Gastrointestinal Function at a High Risk for Invasive Fungal Infection
PI David Helfgott, MD
Contact Tania Curcio, RN
212-746-2571
Key Eligibility

Patients at least 18 years old at high risk of poor enteral medication absorption, based on the effects of cytotoxic chemotherapy, including but not limited to, mucositis, nausea, vomiting, and diarrhea at baseline. Patients must be at high risk for invasive fungal infection.

Treatment Overview

All subjects will receive Posaconazole 200 mg three times daily (TID) for Days 1 to 8. On Day 8, subjects will be randomized to one of three dosing regimens to commence on Days 9 to 15:

Group 1: POS 200 mg TID
Group 2: POS 400 mg BID
Group 3: POS 400 mg TID

 

  Last updated: July 30, 2008
© Weill Medical College of Cornell University
Home | Privacy Notice | Disclaimer