Developing novel therapeutics for unmet medical needs.
Our focus...
We maintain a collaborative work environment where brilliant scientists share our mission to improve the lives of people with rare diseases, delivering on the promise of novel antibody therapeutics.
Partnering on the promise to help patients thrive.
Having a rare disease is bad enough.
Having no promise of effective treatment is worse.
At Mabwell Therapeutics, we explore, discover, and develop the promise of antibody-based drugs to fight rare diseases at the molecular level. With innovation at our core and patients at the heart of everything we do, we are developing a pipeline of meaningful, life-changing therapies for those who need them most.
Mabwell Therapeutics operates as an independent drug discovery group within the Mabwell (Shanghai) Bioscience family of companies. We benefit from access to the full capabilities of our parent organization, enabling us to advance biotherapeutic programs from early research through IND and into commercialization.
Welcoming partners and in-licensing opportunities.
We welcome inquiries from companies and biotech investors who recognize the promise of novel therapeutic biologics in the fight against rare diseases and are interested in helping build the pipeline for effective new drugs in the United States. We also seek in-licensing opportunities for novel therapeutics to initiate clinical testing and registration in China. Contact us to get the conversation started.
New molecular drugs offer promising treatments for devastating rare diseases.
At Mabwell Therapeutics, we help keep the promise.
Innovation Team
Mabwell Therapeutics is led by an experienced team of scientists who share a passion for the promise of molecular medicine. Backed by disciplined research and a panel of expert advisors, we are transforming advanced science into novel therapies for people with rare diseases.

Lei Huang, Ph.D.
Director, Antibody Engineering

Buxin Chen, Ph.D.
Associate Director, Biology
Advisory Board
Our Journey
Our company began with a bold mission: to transform the lives of patients with rare diseases through groundbreaking antibody therapeutics.
Defined our focus to developing therapies for rare, debilitating diseases. Built in-house antibody discovery capabilities to accelerate targeted drug development.
Identified our first lead molecule from program MWTX-003 targeting TMPRSS6 (Transmembrane serine protease 6), advancing to CMC development and preclinical testing.
Achieved our first major regulatory success with IND clearance of the anti-TMPRSS6 monoclonal antibody, an important milestone validating our antibody discovery engine. In parallel, multiple lead candidates were advanced across the pipeline.
Entered an exclusive global licensing agreement with Disc Medicine for our TMPRSS6-targeting antibody portfolio.
Dosed first subject in First-in-human Phase I clinical trial for anti-TMPRSS6 antibody.
Received FDA Orphan Drug Designation for our TMPRSS6-targeting antibody for the treatment of polycythemia vera, marking a significant step in advancing therapies for rare hematologic diseases. In parallel, we expanded our innovation capabilities by building a proprietary NMJ-targeted delivery platform, specially designed to improve outcomes for individuals with neuromuscular disorders.
With a robust pipeline and innovative platforms, we continue to push boundaries in rare disease therapeutics - committed to delivering hope where unmet needs persist.


