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Industry Profile

Rare Disease Therapeutics

Target researchers — Molecular geneticists, enzymologists, and translational researchers specializing in enzyme replacement therapy, gene therapy, antisense oligonucleotides, substrate reduction, and natural history characterization of ultra-rare conditions

Rare disease therapeutics address conditions affecting fewer than 200,000 patients using gene therapy, enzyme replacement, and RNA modulation. Orphan drug designation and premium pricing support returns despite small patient pools, making this industry highly motivated to partner with academic researchers who own rare disease cohorts, biobanks, and foundational mechanistic IP.

$230B Market size
10 Key companies
6 Use cases

Key Companies

Alexion AstraZeneca Sarepta Therapeutics BioMarin Pharmaceutical Ultragenyx Genzyme Sanofi Horizon Therapeutics Amicus Therapeutics Rhythm Pharmaceuticals Entrada Therapeutics Praxis Precision Medicine

Use Cases

01

Orphan gene therapy IP licensing

02

ASO chemistry platform access

03

Disease natural history research partnerships

04

Patient registry collaboration

05

Biomarker development for IND-enabling work

06

ERT enzyme manufacturing partnerships

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