Company Overview | Belief BioMed Inc.

Company Introduction

Belief BioMed Inc. (BBM) is a biotech company that integrates the research & development, manufacturing and clinical application of gene therapy products. The company is committed to providing innovative and more effective gene therapies for severe genetic and chronic diseases through safe and efficient viral vector technology.

BBM has developed hundreds of key vector technologies, including HEK293 cell suspension serum-free culture process and full-scale chromatography purification process, and has established the commercial production platform for gene therapy drugs in China. The company has been building up its capabilities in a variety of fields including novel adeno-associated virus (AAV) capsids targeting different tissues, efficient transgene expression cassette design, and advanced clinical-grade vector manufacturing process. It has also established an extensive R&D pipeline covering a wide range of major, unmet medical needs in therapeutic areas such as hemophilia, Parkinson's disease, arthritis, neuromuscular disease, etc. Several product pipelines have entered clinical studies or submitted IND filings.

In 2021, the Clinical Trial Application (CTA) for BBM-H901, an AAV gene therapy drug for prevention of bleeding in adult male patients with hemophilia B, which was independently developed and manufactured by Belief BioMed, was officially approved by China National Medical Products Administration (NMPA). It is the first gene therapy under development for treatment of hemophilia in China. In 2022, the results of clinical studies related to BBM-H901 were successively published in two prestigious international journals, i.e. The Lancet Haematology and New England Journal of Medicine. In the same year, BBM-H901 was granted Orphan Drug Designation (ODD) by U.S. Food and Drug Administration (FDA), and Breakthrough Therapy Designation (BTD) by China Center for Drug Evaluation (CDE), NMPA.

Vision And Mission

Our Vision

To be a global leader in gene therapy with innovative treatments for patients worldwide.

Our Mission

To make cutting-edge gene therapy drugs that are accessible and affordable.

Key Milestones

2018

May - Belief BioMed group was established.

October - Belief BioMed CMC Center was established.

December - Belief BioMed AAV 15L suspension process was put into production.

2019

October - Belief BioMed Rodent Animal Experiment Center officially commenced operations.

November - BBM-H901 (Hemophilia B) Investigator-initiated Trial (IIT) 1001 was officially started; Dosing of the first subject in IIT was completed.

2020

April - Belief BioMed AAV 200L suspension process was put into production.

October - Belief BioMed Min-hang R&D Center officially commenced operations.

October - Belief BioMed Non-human Primate (NHP) Animal Experiment Center officially commenced operations.

2021

January - Dosing of all subjects in BBM-H901 (Hemophilia B) Investigator-initiated Trial (IIT) was completed.

April - Investigational New Drug (IND) application of BBM-H901 (Hemophilia B) was accepted by the CDE, NMPA.

May - Belief BioMed AAV 500L suspension process was put into production.

August - The registrational clinical trial of BBM-H901 (Hemophilia B) was approved by the CDE, NMPA.

December - Dosing of the first subject in BBM-H901 (Hemophilia B) registrational clinical trial was completed.

2022

May - Results of clinical studies related to BBM-H901 (Hemophilia B) were published in the prestigious international journal The Lancet Haematology.

July - BBM-H803 (Hemophilia A) Investigator-initiated Trial (IIT) was officially started; Dosing of the first subject in IIT was completed.

August - Belief BioMed Commercial Manufacturing Center in the Lin-gang Special Area, with an area of 15,000 square meters, officially commenced operations.

August - BBM-H901 (Hemophilia B) was granted Orphan Drug Designation (ODD) by U.S. FDA.

August - BBM-H901 (Hemophilia B) was granted Breakthrough Therapy Designation (BTD) by the CDE, NMPA.

September - BBM-A101 (Osteoarthritis) Investigator-initiated Trial (IIT) was officially started; Dosing of the first subject in IIT was completed.

October - Results of clinical studies related to BBM-H901 (Hemophilia B) were published in the prestigious international journal New England Journal of Medicine.

December - BBM-H803 (Hemophilia A) was granted Orphan Drug Designation (ODD) by U.S. FDA.

2023

January - Belief BioMed AAV 2000L suspension process was put into production.

April - Dosing of all subjects in the phase III registrational trial of BBM-H901 (Hemophilia B) was completed.

April - Dosing of the first subject in BBM-H901 (Hemophilia B) Investigator-initiated Trial (IIT) 1002 was completed.

July - The registrational clinical trial of BBM-H803 (Hemophilia A) was approved by the CDE, NMPA.

September - Belief BioMed and ThermoFisher reached a strategic cooperation agreement in the field of gene therapy innovative R&D, production and commercialization.

October - Belief BioMed and Takeda China reached exclusive commercial partnership in the field of Hemophilia B in China.

November - Mianyi Biopharmaceutical, subsidiary of Belief BioMed, received the certification for Environmental Management System (ISO14001), and Occupational Health and Safety Management System (ISO45001).

2024

January - Dosing of the first subject in BBM-H803 (Hemophilia A) registrational clinical trial was completed.

January - Mianyi Biopharmaceutical, subsidiary of Belief BioMed, was granted the Drug Manufacturing License “C” by Shanghai Drug Administration.

June - Results of clinical studies related to BBM-H901 (Hemophilia B) were announced in an oral presentation at the ISTH 2024 Congress.

July - Shanghai Xinzhi BioMed, subsidiary of Belief BioMed, was granted Drug Manufacturing License “B” by Shanghai Drug Administration.

July - The New Drug Application (NDA) of BBM-H901 (Hemophilia B) was accepted by CDE, NMPA.

August - The New Drug Application (NDA) of BBM-H901 (Hemophilia B) was granted a Priority Review Designation by the CDE, NMPA.