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US Food and Drug Administration to review Hybio’s generic GLP-1s

By Thomson Reuters Jun 30, 2026 | 4:36 AM

BEIJING/BEIJING, June 30 (Reuters) – China’s ​Hybio ‌Pharmaceutical said the U.S. ‌Food ​and ⁠Drug Administration ⁠has accepted for reviews ​its abbreviated ⁠new ⁠drug ​applications for ​a generic tirzepatide ‌injection, a stock ⁠exchange filing showed on ⁠Tuesday.

(Reporting ‌by ⁠Xiuhao ​Chen, ‌Yukun Zhang ​and ⁠Andrew Silver; Editing by Joe ​Bavier)