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Medera Inc.

June 18, 2025
Company Presentation
Cell and Gene Therapy and Genome Editing
153A
Medera Inc. is a clinical-stage biotechnology company focused on developing treatments for difficult-to-treat cardiovascular diseases through next-generation AAV gene therapy. We leverage our bioengineered human "mini-Heart"platform for disease modeling, preclinical screening, and drug discovery and our proprietary intracoronary delivery technology to address major challenges associated with gene therapy. Led by world-renowned pioneers in cell and gene therapy for cardiovascular disease, we have developed a pipeline comprised of treatments for highly prevalent indications, such as heart failure with preserved ejection fraction (HFpEF) and heart failure with reduced ejection fraction (HFrEF), as well as orphan disease like Duchenne muscular dystrophy-associated cardiomyopathy (DMD-CM). Our HFpEF and HFrEF programs have demonstrated promising human proof-of-concept in Phase 1/2 trials, and we have recently initiated a Phase 1/2 trial for DMD-CM with interim data expected in mid-2026.
Medera Inc.
Company HQ City: Boston
Company HQ State: MA
Company HQ Country: United States
Year Founded: 2014
Lead Product in Development: The Company's lead program is SRD-002 which has demonstrated promising Phase 1/2 efficacy and safety for heart failure with preserved ejection fraction. We intend to initiate a pivotal trial by the end of 2025. We are also developing SRD-003 for Duchenne muscular dystrophy-associated cardiomyopathy and SRD-001 for heart failure with reduced ejection fraction, both in Phase 1/2 trials.

CEO

Ronald Li, Ph.D. (Chairman and CEO)

Development Phase of Lead Product

Phase II

Number of Unlicensed Products Looking for Licensing

The Company's pipeline programs are wholly-owned by Medera.

What is your next catalyst (value inflection) update?

We will have additional Phase 1/2 data for SRD-002 for heart failure with preserved ejection fraction and SRD-001 for heart failure with reduced ejection fraction in the second half of 2025. We expect interim data for SRD-003 for Duchenne muscular dystrophy-associated cardiomyopathy in mid-2026

Website

https://www.medera.bio/
Primary Speaker
James Kim
James Kim
Chief Corporate Officer
Medera Inc.
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