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Brief Title: A Phase I Dose Escalation Trial of PR104 Given Weekly in Subjects With Solid Tumors
Official Title: A Phase I, Multi-center, Open-label, Dose Escalation Trial of the Safety and Pharmacokinetics of Intravenous PR104 Given Weekly in Subjects With Solid Tumors
Study ID: NCT01358227
Brief Summary: The purpose of this study is to determine the side effects and best weekly dose of PR104 in patients with advanced solid tumors.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Auckland, Auckland, , New Zealand
Waikato Hospital, Waikato, , New Zealand
Name: Mark McKeage, PhD, FRACP
Affiliation: University of Auckland, New Zealand
Role: PRINCIPAL_INVESTIGATOR