Condition: Non-Familial Hypercholesterolemia and Mixed Hyperlipidemia · Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
This is a multi-center, randomized, double-blind, placebo-controlled phase III clinical study evaluating the efficacy and safety of IBI306 monotherapy in Chinese Paricipants with non-familial hypercholesterolemia and mixed hyperlipidemia. Approximately 198 participants were planned to be enrolled in the study. The entire study period includes a screening period of no more than 2 weeks, a run-in period of 4 weeks, a double-blind treatment period of 12 weeks, and a safety follow-up period after the last treatment. Participants were required to maintain a stable and healthy lifestyle throughout the trial.
This description comes directly from the study's public registry record.
Yida Tang · 010-82266699 · tang_yida@163.com
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| Peking University Third Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07473960