Drug Profile

Research programme: muscle wasting disease therapies - Immusoft

Latest Information Update: 28 Sep 2024

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity No

No development reported Amyotrophic lateral sclerosis; Duchenne muscular dystrophy

28 Sep 2024 No recent reports of development identified for preclinical development in Amyotrophic-lateral-sclerosis in USA (Parenteral, Injection)
28 Sep 2024 No recent reports of development identified for preclinical development in Duchenne muscular dystrophy in USA (Parenteral, Injection)
26 Aug 2020 Preclinical trials in Amyotrophic lateral sclerosis in USA (Parenteral) (Immusoft pipeline, August 2020)

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