MedPath

LUZHU BIOTECH-B

🇭🇰Hong Kong, China
Ownership
-
Established
2001-11-09
Employees
148
Market Cap
-
Website
http://www.luzhubiotech.com
Introduction

The company is a biotechnology company dedicated to developing innovative human vaccines and therapeutic biologics to prevent and control infectious diseases and treat cancer and autoimmune diseases.

Since its establishment in 2001, the Group has focused on the field of human medicine, and has established a technical platform based on its understanding of immunology and protein engineering, so that the Group can develop recombinant vaccines and antibody products with improved efficiency, high purity and stability.

As of June 30, 2024, the Group's product pipeline includes three clinical-stage products under development, one of which is the core product LZ901, and four pre-clinical products under development.

As of June 30, 2024, the Group has five R&D patents related to core products and four pending approval applications. All registered patents and patent applications for core products relate to the same set of patent claims filed in nine different jurisdictions to protect the core product. This is because in addition to China and the US, other jurisdictions are also future target markets or potential markets for LZ901.

The Company's H shares were listed on the Stock Exchange on May 8, 2023. The total net proceeds of the Company's global offering of H shares (“Global Offering”) (net of underwriting commissions and other expenses payable by the Company in connection with the global offering) is approximately HK$241.6 million.

Luzhu Biotech's Novel Herpes Zoster Vaccine Advances as NMPA Accepts Regulatory Filing

• Beijing Luzhu Biotechnology has achieved a significant regulatory milestone as China's NMPA accepts the biologics license application for its recombinant herpes zoster vaccine LZ901. • The vaccine, targeting adults aged 40 and above, has successfully met its Phase III clinical trial endpoints, positioning it as a potential new preventive option for shingles. • While the acceptance enables further regulatory evaluation, the company maintains cautious outlook regarding the ultimate development and commercialization success.
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