Lexeo wins fast track designation for Friedreich’s ataxia gene therapy
Clinical-stage genetic medicine company Lexeo Therapeutics has won fast track designation from the US Food and Drug Administration (FDA) for…
Clinical-stage genetic medicine company Lexeo Therapeutics has won fast track designation from the US Food and Drug Administration (FDA) for…
Spinogenix has received approval from the US Food and Drug Administration (FDA) for a Phase II clinical trial of SPG601…
The US Food and Drug Administration (FDA) has granted orphan drug designation to the active ingredient in MarVax, Soligenix’s vaccine…
South Korea-based SK Life Sciences has received US Food and Drug Administration (FDA) approval for two new forms of administration…
The National Institute for Health and Care Excellence (NICE) has issued a final draft guidance recommending the use of AbbVie’s…
Innate Pharma has announced positive preclinical data of its antibody-drug conjugate (ADC) candidate IPH45, as it plans to advance the…
Oryzon Genomics is set to commence a Phase I/II clinical trial of iadademstat (ORY-1001) plus immune checkpoint inhibitors (ICI) in…
A new drug application (NDA) from US-Ireland speciality pharmaceutical company Shorla Oncology has been accepted by the US Food and…
Amylyx Pharmaceuticals has formally announced the removal of its amyloid lateral sclerosis (ALS) drug Relyvrio (AMX0035) from the market following…
UK-based CDMO Touchlight has teamed up with the University of Liverpool, UK, to utilise its doggybone DNA (dbDNA) technology in…