EpimAb Biotherapeutics Announces FDA Clearance of its IND Application for EMB-02, a Bispecific Dual Checkpoint Inhibitor

IND filing of second bispecific antibody candidate developed from EpimAb’s FIT-Ig® platform

SHANGHAI--()--EpimAb Biotherapeutics, a clinical stage biotech company specializing in bispecific antibodies, today announced that it has received “STUDY MAY PROCEED” letter from the U.S. Food and Drug Administration (FDA) on an Investigational New Drug (IND) application for the Company’s second therapeutic development candidate, EMB-02. The application was submitted to the FDA to investigate the treatment of solid tumors with EpimAb’s novel bispecific antibody.

The advancement of our second bispecific antibody into the clinic expands our clinical portfolio and also shows that our FIT-Ig® technology can generate a variety of clinical candidates,” commented Dr. Chengbin Wu, founder and CEO of EpimAb Biotherapeutics. “We expect to file additional applications in the near future for novel bispecific antibody programs being developed to treat patients suffering from serious cancer types. In 2021, we expect to have a total of three programs under investigation in clinical trials.”

EMB-02 is a bispecific antibody based on EpimAb’s proprietary FIT-Ig® (Fabs-In-Tandem Immunoglobulin) technology to generate bispecific molecules with superior properties. EMB-02 simultaneously targets two checkpoint proteins, PD-1 and LAG-3, and has shown strong anti-tumor activities in preclinical models resistant to standard anti-PD-1 monotherapies.

While EMB-02 is progressing towards the clinic, EpimAb continues to investigate EMB-01, its lead candidate, in a Phase I/II clinical study in both China and the U.S., and is generating several additional biologics, creating a proprietary pipeline based on its FIT-Ig® platform. These earlier-stage assets are focused on immuno-oncology approaches in areas of high unmet medical need in cancer.

About EpimAb Biotherapeutics, Inc.

EpimAb Biotherapeutics is a privately-owned biopharmaceutical R&D company with research and manufacturing facilities in Shanghai and Suzhou with a proprietary unique and efficient technology called FIT-Ig® (Fabs-In-Tandem Immunoglobulin) to generate bispecific molecules with antibody-like properties. With this platform EpimAb is creating a pipeline of its own novel bispecific antibody therapeutics focused around immuno-oncology and other areas of high value to patients. EpimAb is also committed to diversifying its pipeline through selective licensing of its platform and pipeline assets to partners worldwide. For further information, please visit www.epimab.com

Contacts

EpimAb Biotherapeutics
In the U.S.:
Dr. Stephan Lensky, COO/CBO
Direct: +1 978-870-6276
Stephan.lensky@epimab.com

In China:
Dr. Jason Tang,BD Director
Direct: +86-21- 61951000
E-Mail: yesheng.tang@epimab.com

Media Inquiries
MacDougall
Amanda Houlihan
+1 781-235-3060
epimab@macbiocom.com

Release Summary

EpimAb announces that it has received “STUDY MAY PROCEED” letter from the U.S. FDA for an IND application for EMB-02.

Contacts

EpimAb Biotherapeutics
In the U.S.:
Dr. Stephan Lensky, COO/CBO
Direct: +1 978-870-6276
Stephan.lensky@epimab.com

In China:
Dr. Jason Tang,BD Director
Direct: +86-21- 61951000
E-Mail: yesheng.tang@epimab.com

Media Inquiries
MacDougall
Amanda Houlihan
+1 781-235-3060
epimab@macbiocom.com