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Brief Title: First in Human Trial of TAS266 in Patients With Advanced Solid Tumors
Official Title: A Phase I, Open-label Dose Escalation Study With Safety Expansion of TAS266 Administered by IV Infusion to Patients With Advanced Solid Tumors
Study ID: NCT01529307
Brief Summary: This study will assess safety, tolerability, maximum tolerated dose or recommended dose for expansion of TAS266 administered by IV infusion to patients with advanced solid tumors.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
H. Lee Moffitt Cancer Center/University of South Florida Moffitt SC, Tampa, Florida, United States
South Texas Accelerated Research Therapeutics START, San Antonio, Texas, United States
University of Utah / Huntsman Cancer Institute Huntsman UT, Salt Lake City, Utah, United States
Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR