FDA grants RMAT designation to AbelZeta’s CAR-T therapy
The US Food and Drug Administration (FDA) has granted regenerative medicine advanced therapy (RMAT) designation to AbelZeta Pharma’s autologous bi-specific …
The US Food and Drug Administration (FDA) has granted regenerative medicine advanced therapy (RMAT) designation to AbelZeta Pharma’s autologous bi-specific …
In the race to decarbonize the global economy, advanced materials are no longer a luxury - they're a necessity. The …
The global cell and gene therapy (CGT) market is expanding at a rapid rate, and will be worth $76bn by …
The US Centers for Disease Control and Prevention (CDC) is no longer recommending Covid-19 vaccines to healthy children and pregnant …
Biotechnology company GlycoEra has closed an oversubscribed Series B financing round, raising $130m, to support the progression of its lead …
Biogen and City Therapeutics are to partner for the development of new RNA interference (RNAi) therapies. Leveraging tissue-enhanced delivery technologies, the …
Cell and gene therapy (C>) represents a major advance in medical treatments by directly targeting the root causes of diseases …
Eli Lilly has agreed to acquire privately held biopharma company SiteOne Therapeutics, adding a non-opioid-based pain treatment to the big …
Representatives of industry and regulation will meet in June to discuss paths forward for the UK’s clinical trials sector following …
GSK has made a new drug submission (NDS) to Health Canada for the monoclonal antibody, depemokimab, targeting two specific conditions. The …
With the 78th World Health Assembly ending today, all eyes have been on this year’s World Health Organization (WHO) member’s …
Lupin has signed a licence and supply agreement with SteinCares to commercialise its biosimilar ranibizumab in Latin American markets, excluding …
The US Food and Drug Administration (FDA) has accepted Otsuka Pharmaceutical’s biologics licence application for sibeprenlimab for review. The monoclonal …
Upperton Pharma Solutions (Upperton), a contract development and manufacturing organization (CDMO) based in the UK, won the Business Expansion award …
The European Medicines Agency (EMA) has validated the marketing authorisation application (MAA) submitted by Soleno Therapeutics for diazoxide choline prolonged-release …