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YS Biopharma reports progress in rabies vaccine trial

EditorEmilio Ghigini
Published 09/04/2024, 14:26
LSB
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GAITHERSBURG, Md. - YS Biopharma Co., Ltd. (NASDAQ: YS) has announced interim results from a Phase 3 clinical trial of its PIKA Rabies Vaccine, indicating the vaccine met primary endpoints for accelerated protection against rabies. The trial results suggest the vaccine could offer a one-week regimen, potentially replacing the current three- or four-week schedules and aligning with the World Health Organization's goals.

The vaccine uses YS Biopharma's proprietary PIKA adjuvant technology, which is intended to elicit a stronger immune response more rapidly than existing vaccines. The US FDA has granted it orphan drug designation for the prevention of rabies virus infection, including post-exposure prophylaxis (PEP).

The ongoing multicenter trial involves 4,500 participants from the Philippines and Pakistan, comparing the PIKA Rabies Vaccine administered over seven days to a globally marketed vaccine given over 28 days. Interim data from the first 900 participants show that the PIKA vaccine achieved twice the seroconversion rate by Day 7 compared to the comparator, without compromising safety.

Dr. Zenaida Mojares, Chief Medical Officer of YS Biopharma, highlighted the vaccine's robust immunogenicity and favorable safety profile, noting its potential to improve treatment compliance due to the shortened regimen. Dr. David Shao, the company's CEO, expressed gratitude to trial participants and investigators, emphasizing the vaccine's expected contribution to reducing immune failure rates.

YS Biopharma is a global biopharmaceutical company focused on vaccines and therapeutic biologics for infectious diseases and cancer. The company, with operations in China, the United States, Singapore, and the Philippines, is pursuing regulatory approvals in various countries for the PIKA Rabies Vaccine.

This article is based on a press release statement from YS Biopharma.

InvestingPro Insights

YS Biopharma, while advancing in the clinical trial phase for its PIKA Rabies Vaccine, presents a mixed financial picture according to real-time data from InvestingPro. The company's gross profit margin stands at an impressive 80.05% for the last twelve months as of Q2 2024, pointing to a strong ability to generate profit from sales. However, the company is also experiencing a rapid cash burn, which is a critical factor for investors to consider, especially given the capital-intensive nature of biopharmaceutical ventures.

InvestingPro Data highlights a market capitalization of 165.73 million USD, which reflects the current valuation of the company within the market. The revenue has seen a decline of 11.42% over the last twelve months as of Q2 2024, and an even sharper quarterly revenue growth decrease of 50.11% in Q2 2024. This could be indicative of the challenges YS Biopharma faces in a competitive biopharmaceutical landscape or a strategic realignment of its operations. Additionally, the price of YS Biopharma's stock has experienced a significant return over the last week, with a 17.49% increase, which may be influenced by the positive news from the clinical trial results.

InvestingPro Tips for YS Biopharma include the stock's high price volatility, which suggests that investors should be prepared for potentially significant fluctuations in stock price. Furthermore, analysts do not anticipate the company to be profitable this year, a factor that could weigh on investment decisions.

For those interested in a deeper dive into the financials and future prospects of YS Biopharma, InvestingPro offers additional insights and metrics. To explore these, visit https://www.investing.com/pro/YS for more detailed analysis. Remember to use the coupon code PRONEWS24 to get an additional 10% off a yearly or biyearly Pro and Pro+ subscription, unlocking even more valuable InvestingPro Tips — there are 16 additional tips listed for YS Biopharma on InvestingPro that could provide further guidance for your investment strategy.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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