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Sardocor

Lexington, Massachusetts, United Statessardocor.com ↗

Ownership: Private
Development stage: Phase 1

Overview

Sardocor has three ongoing FDA-approved AAV-based gene therapy clinical trials targeting HFrEF, HFpEF, and DMD-CM. SRD‑001 has received Fast Track designation from the FDA for HFpEF. The company uses a proprietary intracoronary delivery method to enhance efficacy and safety by reducing required viral titers. Interim data are positive; over a thousand doses of SRD‑001 have been manufactured. Orphan Drug Designation was granted for the DMD program. Preclinical pipeline includes additional gene therapies and small molecules.

Therapeutic areas: Cardiovascular
Modalities: Gene therapy (AAV-based)Small molecules (preclinical pipeline)
Industry: Biotech

Drug pipeline

13 assets

AAV1/SERCA2a

12 more assets in the full pipeline.

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Partnerships

Collaboration/licensing arrangements with global pharmaceutical leaders mentioned but not specified by name

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