[{"orgOrder":0,"company":"AVAS Pharmaceuticals","sponsor":"Lupin Ltd","pharmaFlowCategory":"DU","therapeuticArea":"Genetic Disease","country":"INDIA","productType":"Other Small Molecule","year":"2025","type":"Inapplicable","leadProduct":"Mexiletine","moa":"||Na channel-alpha-subunit","graph1":"Genetic Disease","graph2":"Approved FDF","graph3":"AVAS Pharmaceuticals","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Genetic Disease","amount2New":0,"dosageForm":"Oral Capsule","sponsorNew":"AVAS Pharmaceuticals \/ AVAS Pharmaceuticals","highestDevelopmentStatusID":"15","companyTruncated":"AVAS Pharmaceuticals \/ AVAS Pharmaceuticals"}]

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                          EPSC
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                          EPSC
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                          Details : NaMuscla (mexiletine hydrochloride) is a Sodium channel alpha subunit blocker, being evaluated for the symptomatic treatment of myotonia in adults with non-dystrophic myotonic (NDM) disorders.

                          Product Name : Namuscla

                          Product Type : Other Small Molecule

                          Upfront Cash : Inapplicable

                          January 28, 2025

                          Lead Product(s) : Mexiletine,Inapplicable

                          Therapeutic Area : Genetic Disease

                          Highest Development Status : Approved FDF

                          Recipient : Lupin Ltd

                          Deal Size : Inapplicable

                          Deal Type : Inapplicable

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