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Clinical Trial Summary

This is a phase 1 open label multicentre study of SHR9549 administered orally in patients with advanced estrogen receptor (ER) positive human epidermal receptor 2 (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(MTD). In addition, expansion cohort(s) at potential therapeutic dose(s) in patients will be enrolled to further determine the safety, tolerability, pharmacokinetics and biological activity of SHR9549.


Clinical Trial Description

A Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of Ascending Doses of SHR9549 in Women with Estrogen Receptor (ER) Positive Human Epidermal Receptor (HER-2) Negative Advanced Breast Cancer ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03596658
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact
Status Terminated
Phase Phase 1
Start date July 25, 2018
Completion date October 14, 2019

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04541433 - A Phase 1 Study of AZD9833 in Japanese Women With ER Positive, HER2 Negative Advanced Breast Cancer Phase 1
Completed NCT02248090 - AZD9496 First Time in Patients Ascending Dose Study Phase 1
Active, not recruiting NCT03616587 - Study of AZD9833 Alone or in Combination in Women With Advanced Breast Cancer. Phase 1
Recruiting NCT06188520 - A First-in-human Dose Escalation and Expansion Study to Evaluate the Safety, and Tolerability of AZD8421 Alone or in Combination in Participants With Selected Advanced or Metastatic Solid Tumors Phase 1/Phase 2