Core Viewpoint - Lepu Medical (300003.SZ) has received approval from the National Medical Products Administration (NMPA) for its subsidiary Lepu Jiantang Pharmaceutical (Chongqing) Co., Ltd. to conduct clinical trials for its self-developed injectable recombinant type A botulinum toxin [1] Group 1 - The clinical trial application for the injectable recombinant type A botulinum toxin (LPJT-099/DP) has been approved, indicating progress in the company's research and development efforts [1] - The amino acid sequence of the company's injectable recombinant type A botulinum toxin is identical to that of Botox® and Xeomin®, suggesting a competitive edge in the market [1] - The product is developed using recombinant protein technology, which offers advantages such as low biological risk, high purity, low immunogenic risk, high production efficiency, and controllable capacity [1] Group 2 - The advancement of this project signifies the company's strong and efficient R&D capabilities in the dermatology field, enhancing its product portfolio in this sector [1] - This development is expected to strengthen the company's core competitiveness in the dermatology niche and support its long-term growth in the consumer healthcare market [1]
乐普医疗(300003.SZ):注射用重组A型肉毒毒素临床试验申请获得批准