-
Topline Results AbbVie – Calico eIF2B Activator Fosigotifator
The Sean M. Healey & AMG Center for ALS at Massachusetts General Hospital announced topline results from Regimen F of the HEALEY ALS Platform Trial evaluating fosigotifator (ABBV-CLS-7262) in people… More >>
-
Topline Results Denali Therapeutics eIF2B Agonist DNL343
The Sean M. Healey & AMG Center for ALS at Massachusetts General Hospital announced topline results from an analysis of Regimen G evaluating DNL343, an eIF2B agonist developed by Denali… More >>
-
Corcept Announces Results From Phase 2 DAZALS Study of Dazucorilant in ALS
Corcept Therapeutics, a commercial-stage company engaged in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic, and neurologic disorders by modulating the effects of the hormone cortisol,… More >>
-
Topline results PTC Therapeutics cardinALS trial
– Study failed to meet primary and secondary efficacy endpoints – PTC Therapeutics announced that the global Phase 2 placebo-controlled CardinALS study did not meet its primary endpoint of slowing… More >>
-
Biogen published results of Phase I study with BIIB078 C9orf72 ASO
Biogen published Safety, tolerability, and pharmacokinetics of antisense oligonucleotide BIIB078 in adults with C9orf72-associated amyotrophic lateral sclerosis: a phase 1, randomised, double blinded, placebo-controlled, multiple ascending dose study Background Hexanucleotide… More >>
-
uniQure Announces Dosing of First Patient in Phase I/II Clinical Trial of AMT-162 for the Treatment SOD1-ALS
uniQure, a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced that the first patient has been dosed in the Phase I/II clinical trial… More >>
-
Decoding regulatory agency decisions – The case of Amylyx’s Relyvrio-Albrioza in the US and EU
Amylyx’s ill fated treatment for amyotrophic lateral sclerosis, was approved for marketing by the US Food and Drug Administration but rejected by the European Medicines Agency. The Pink Sheet explores… More >>
-
Biogen Receives European Commission Approval for QALSODY® (tofersen)
Biogen announced the European Commission (EC) has granted marketing authorization under exceptional circumstances and maintained orphan designation for QALSODY® (tofersen) for the treatment of adults with amyotrophic lateral sclerosis (ALS)… More >>

