Core Viewpoint - Lu Kang Pharmaceutical has received approval from the National Medical Products Administration for the market entry of Celecoxib, marking a significant milestone after substantial R&D investment [1][5]. Group 1: Product Approval and Market Potential - Celecoxib, developed by Pfizer, is the first selective COX-2 inhibitor approved globally, used for treating conditions like osteoarthritis, rheumatoid arthritis, acute pain, and ankylosing spondylitis [5]. - In 2023, sales of Celecoxib capsules in China's major markets exceeded 800 million yuan, ranking among the top 8 products in the category of oral anti-inflammatory and anti-rheumatic drugs, with a projected growth of 5.05% in the first half of 2024 [5]. - The demand for Celecoxib raw materials in China has been increasing, with usage rising from 91.62 tons in 2022 to 109.7 tons in 2023, reflecting a year-on-year growth rate of 19.7% [5]. Group 2: Competitive Landscape and Company Strategy - There are currently 53 registered raw material drug numbers for Celecoxib in China, with 38 passing the review process, indicating a competitive market [5]. - Companies like Hengrui Medicine and CSPC Pharmaceutical have already secured bids in the third batch of national centralized procurement for Celecoxib capsules [5]. - Lu Kang Pharmaceutical has invested a total of 14.899 million yuan in the R&D of Celecoxib raw materials, positioning itself for future product quality control and cost management advantages [5][7]. Group 3: Company Performance and Market Response - Lu Kang Pharmaceutical has shown steady revenue growth, with projected revenue of 6.233 billion yuan in 2024, a year-on-year increase of 1.41%, and a net profit of 408 million yuan, up 59.02% [7]. - The company's stock price has increased by 8.16% year-to-date, closing at 10.33 yuan per share on May 8, 2023, despite a slight daily decline [7].
研发投入超千万!鲁抗医药新药获批上市,公司回应:将积极争取集采