Study of Subcutaneous Rehydration With Recombinant Human Hyaluronidase for Infants and Children

PHASE4CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

August 31, 2007

Primary Completion Date

June 30, 2008

Study Completion Date

June 30, 2008

Conditions
Dehydration
Interventions
DRUG

hyaluronidase (human recombinant)/rehydration fluid

Single 150 U subcutaneous (SC) HYLENEX dose administered immediately prior to start of SC infusion of rehydration fluid. Additional 150 U HYLENEX dose to be administered prior to any additional fluid infusion beyond 24 hours.

All Listed Sponsors
collaborator

Halozyme Therapeutics

INDUSTRY

collaborator

PPD Development, LP

INDUSTRY

lead

Baxter Healthcare Corporation

INDUSTRY