The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: AZD9496 First Time in Patients Ascending Dose Study
Official Title: Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of Ascending Doses of AZD9496 in Women With Estrogen Receptor Positive HER-2 Negative Advanced Breast Cancer
Study ID: NCT02248090
Brief Summary: This is a phase 1 open label multicentre study of AZD9496 administered orally in patients with advanced ER+ HER2 negative breast cancer. The study design allows an escalation of dose with intensive safety monitoring to ensure the safety of patients. The study will determine the maximum tolerated dose. In addition, expansion cohort(s) at potential therapeutic dose(s) in patients with or without ESR1 mutations will be enrolled to further determine the safety, tolerability, pharmacokinetics and biological activity of AZD9496
Detailed Description: A Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of Ascending Doses of AZD9496 in Women with Estrogen Receptor Positive HER-2 Negative Advanced Breast Cancer
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Florida Cancer Specialists, Sarasota, Florida, United States
Research Site, New York, New York, United States
Sarah Cannon, Nashville, Tennessee, United States
Seoul National Univ. Hospital, Seoul, , Korea, Republic of
Research Site, Cambridge, , United Kingdom
Christie, Manchester, , United Kingdom
Name: Erika Hamilton
Affiliation: Nashville Hospital, United States
Role: PRINCIPAL_INVESTIGATOR
Name: Justin Lindemann
Affiliation: AstraZeneca
Role: STUDY_DIRECTOR