ReCode Therapeutics
ReCode Therapeutics is a clinical-stage genetic medicines company headquartered in Menlo Park, California with operations in Dallas, Texas, founded in 2015 out of research at UT Southwestern. Its Selective Organ Targeting (SORT) lipid nanoparticle platform is a delivery technology that directs mRNA and gene-correction payloads to organs, tissues and cells beyond the liver — the constraint that has limited genetic medicines to date — with redosing capability. Its lead programmes are RCT1100, an inhaled DNAI1 mRNA therapy for primary ciliary dyskinesia which has reported first-ever proof of activity in PCD patients, and RCT2100, an inhaled CFTR mRNA therapy for cystic fibrosis now in a Phase 2 combination trial with ivacaftor; both hold U.S. FDA Orphan Drug designation. The company collaborates with Intellia Therapeutics on CRISPR-based gene correction for cystic fibrosis, is funded in part by the Cystic Fibrosis Foundation, and has raised over $260 million in Series B financing. ReCode Therapeutics runs no developer program and publishes no product API, developer portal or API documentation; the only machine-readable surface reachable without credentials is the WordPress REST content API behind recodetx.com, catalogued here alongside the llms.txt the site publishes.
ReCode Therapeutics publishes 1 API on the APIs.io network. Tagged areas include Company, Genetic Medicine, Biotechnology, Biopharmaceutical, and mRNA.
The ReCode Therapeutics catalog on APIs.io includes 1 JSON-LD context.
ReCode Therapeutics’ developer surface includes product news, authentication, and 31 more developer resources.
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APIs 1
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ReCode Therapeutics Website (WordPress REST)
The public WordPress REST API (wp-json) of the ReCode Therapeutics website at recodetx.com: the route index of the site's content management system, catalogued as one site surfa...
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OPEN COLLECTIONSemantic Vocabularies 1
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Design & Contract 6
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Build 2
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Access & Security 2
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Commercial 2
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Company 9
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Other 9
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