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Spots Global Cancer Trial Database for AZD9496 First Time in Patients Ascending Dose Study

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Trial Identification

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

Interventions

AZD9496
AZD9496

Study Description

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

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

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

Contact Details

Name: Erika Hamilton

Affiliation: Nashville Hospital, United States

Role: PRINCIPAL_INVESTIGATOR

Name: Justin Lindemann

Affiliation: AstraZeneca

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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