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RFUS-949 is a Class 1 new chemical entity (small molecule) developed by Yichang Renfu Pharmaceutical, a subsidiary of Wuhan Humanwell Hi-Tech Industry (Humanwell Healthcare Group). It is formulated as an oral tablet intended for the treatment of acute and chronic pain. In May 2024, the drug received clinical trial approval from China's National Medical Products Administration (NMPA) to initiate Phase 1 clinical studies. These initial trials are designed to evaluate the safety, tolerability, and pharmacokinetic characteristics of RFUS-949 in healthy Chinese subjects. At the time of its clinical entry, the developer noted that no similar products had been approved for marketing in China.
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