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Brief Title: Study of PEGPH20 With Initial Dexamethasone Premedication Given Intravenously to Patients With Advanced Solid Tumors
Official Title: A Phase 1, Multicenter, Open-Label, Dose-Escalation, Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of PEGPH20 With Initial Dexamethasone Premedication Given Intravenously to Patients With Advanced Solid Tumors
Study ID: NCT01170897
Brief Summary: This is an open-label, multicenter, dose-escalation, safety, tolerability, pharmacokinetic and pharmacodynamic study in patients with advanced solid tumors.
Detailed Description: A study of PEGylated recombinant human hyaluronidase (PEGPH20) administered on a twice weekly schedule for 28 days followed by a weekly dosing schedule in patients with advanced solid tumors who have either failed to respond to standard therapy or for whom no standard therapy exists.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Ramesh K. Ramanathan M.D., Scottsdale, Arizona, United States
Mayo Clinic - Scottsdale, Scottsdale, Arizona, United States
cCare - California Cancer Associatesfor Research Excellence, Encinitas, California, United States
Karmanos Cancer Institute, Detroit, Michigan, United States
Jeffrey R. Infante, Nashville, Tennessee, United States
Name: Joy Zhu, M.D.
Affiliation: Halozyme Therapeutics
Role: STUDY_DIRECTOR