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Chinese startup Rona Therapeutics has granted Roche an exclusive worldwide license for Rona's investigational
Nanyang Technological University (NTU), Singapore and global biopharmaceutical company Boehringer Ingelhe
Taiwan-based Foresee Pharmaceuticals has been notified by its licensing partner, Changchun GeneScience Pharmac
The Abu Dhabi Public Health Centre (ADPHC) has signed a strategic Memorandum of Understanding (MoU) with Ultra
The National Centre for Engineering Biology (NCEB), hosted at the National University of Singapore (NUS),
United Immunity, a clinical stage biotechnology company, has raised a total of ¥2.2 billion in private fin
Theramex, a London-headquartered specialty pharmaceutical company dedicated to women and their health, and Chi
HKSH Medical Group (HKSH) and United Imaging Healthcare (United Imaging) have announced the arrival of Hong Ko
GCCL, a South Korea-based leading global clinical trial central laboratory, has signed a Memorandum of Underst
South Korea-based LOTTE Biologics, a contract development and manufacturing (CDMO) organisation, and Alvotech,
Neurology is moving from a history of high-risk failures to a period of unprecedented therapeutic experimentation. For decades, the complexity of the brain, limited understanding of disease biology and the formidable blood-brain barrier (BBB) made central nervous system (CNS) drug development one of pharma’s toughest challenges. That equation is now beginning to shift.
Advances in neurobiology, neuroimmunology, precision medicine and drug-delivery technologies are opening new routes to diseases once considered largely untreatable. Recent approvals have introduced disease-modifying and genetically targeted therapies, while the Phase III pipeline is testing approaches aimed at Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), Dravet syndrome and other neurological disorders.
Behind this momentum is a deeper change: developers are moving beyond managing symptoms towards targeting the biological mechanisms that drive disease. The question now is whether this scientific momentum can finally translate into durable clinical benefit—and make disease modification a repeatable reality in neurology.
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