Armatus Bio


Armatus Bio is pioneering vectorized RNAi therapeutics for genetic neurological and neuromuscular diseases. They focus on precisely targeting disease-driving genes in autosomal dominant neuromuscular disorders, leveraging advanced RNA technology to develop life-changing medicines for conditions with no current therapeutic options. Their mission is to transform outcomes through precision RNAi, addressing significant unmet needs in neuromuscular diseases such as CMT1A and FSHD.

Industries

biopharma
biotechnology
health-diagnostics

Nr. of Employees

small (1-50)

Armatus Bio


Products

AAV-delivered engineered microRNA therapeutic for peripheral nerve disease

Late preclinical program employing an AAV serotype-based vector expressing engineered microRNA to reduce overexpression of a disease-driving gene implicated in peripheral nerve demyelination, developed for one-time intrathecal administration.

Systemic AAV-delivered engineered microRNA therapeutic for muscle disease

Late preclinical program using systemically administered AAV with a myotropic capsid to deliver engineered microRNA that reduces toxic gene expression associated with a muscular dystrophy phenotype.

miRNA payload screening and translational fidelity platform (SPRINT)

Discovery platform for rapid evaluation and prioritization of microRNA payloads with emphasis on translational fidelity to accelerate selection of candidates for preclinical development.

Expertise Areas

  • Vectorized RNAi therapeutics
  • MicroRNA engineering and payload selection
  • AAV vector and capsid engineering
  • Preclinical development and IND-enabling studies
  • Show More (4)

Key Technologies

  • AAV-based vector delivery
  • MicroRNA-based gene silencing
  • miRNA payload screening platform
  • Capsid engineering for tissue tropism
  • Show More (3)

News & Updates

Armatus Bio Selected as Finalist for XPRIZE Healthspan FSHD Bonus Prize

SOLVE FSHD Announces $3 Million Investment in Armatus Bio to Advance Gene Therapy Program for FSHD

Armatus Completes Successful Pre-IND Meeting With the U.S. FDA to Proceed With ARM-201 Development for the Treatment of FSHD

FDA Grants Orphan Drug and Rare Pediatric Designations to ARM-201 for the Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)

Armatus Completes Successful Pre-IND Meeting With the U.S. FDA to Advance TVR110 for the Treatment of CMT1A

FDA Grants Orphan Drug and Rare Pediatric Designations to TVR110 for the Treatment of Charcot-Marie-Tooth Disease Type 1A (CMT1A)


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