Condition: Chronic Stable Angina Pectoris · Sponsor: Tasly Pharmaceuticals, Inc.
This is a multi-center, double-blind, randomized, placebo-controlled, parallel-group phase 3 clinical study to confirm the safety and efficacy of T89 in patients with stable angina pectoris, with an extended open-label period to evaluate the long-term safety of T89. This study includes three main periods: the first study period is a 3-week single-blind qualifying run-in period to screen eligible stable angina patients by exercise tolerance test (ETT). The second study period is a 8-week double-blind treatment period to evaluate the efficacy and safety of T89 in patients with stable angina by ETT. And, the last study period is a 44-week open-label period to observe long-term use safety of T89.
This description comes directly from the study's public registry record.
Henry H Sun, PhD, MD · 301-978-3905 · HSun@taslyUS.com
Ruoling Guo, PhD · RGuo@taslyUS.com
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Source record: clinicaltrials.gov/study/NCT03789552