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 …
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4x the Performance, Zero Compromise: How Functionalized Polymers Are Changing the Rules
In the race to decarbonize the global economy, advanced materials are no longer a luxury - they're a necessity. The …
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How 3PL providers are gearing up for the wave of cell and gene therapies
The global cell and gene therapy (CGT) market is expanding at a rapid rate, and will be worth $76bn by …
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CDC drops Covid-19 vaccine for healthy children and pregnant women
The US Centers for Disease Control and Prevention (CDC) is no longer recommending Covid-19 vaccines to healthy children and pregnant …
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GlycoEra secures $130m to progress IgG4-targeted protein degrader
Biotechnology company GlycoEra has closed an oversubscribed Series B financing round, raising $130m, to support the progression of its lead …
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Biogen and City Therapeutics to develop RNAi therapy
Biogen and City Therapeutics are to partner for the development of new RNA interference (RNAi) therapies. Leveraging tissue-enhanced delivery technologies, the …
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How the cell and gene therapy market is taking shape
Cell and gene therapy (C>) represents a major advance in medical treatments by directly targeting the root causes of diseases …
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Eli Lilly to expand pain pipeline with $1bn SiteOne buyout
Eli Lilly has agreed to acquire privately held biopharma company SiteOne Therapeutics, adding a non-opioid-based pain treatment to the big …
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Capitalising on UK’s goal to become a world-leading clinical trial destination
Representatives of industry and regulation will meet in June to discuss paths forward for the UK’s clinical trials sector following …
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GSK makes new drug submission for depemokimab in Canada
GSK has made a new drug submission (NDS) to Health Canada for the monoclonal antibody, depemokimab, targeting two specific conditions. The …
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What’s been agreed at this year’s World Health Assembly?
With the 78th World Health Assembly ending today, all eyes have been on this year’s World Health Organization (WHO) member’s …
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Lupin partners SteinCares to commercialise biosimilar in LATAM
Lupin has signed a licence and supply agreement with SteinCares to commercialise its biosimilar ranibizumab in Latin American markets, excluding …
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FDA to review Otsuka’s sibeprenlimab application for IgAN
The US Food and Drug Administration (FDA) has accepted Otsuka Pharmaceutical’s biologics licence application for sibeprenlimab for review. The monoclonal …
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Pharmaceutical Technology Excellence Awards 2025: Upperton Pharma Solutions
Upperton Pharma Solutions (Upperton), a contract development and manufacturing organization (CDMO) based in the UK, won the Business Expansion award …
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EMA validates Soleno’s application for Prader-Willi syndrome treatment
The European Medicines Agency (EMA) has validated the marketing authorisation application (MAA) submitted by Soleno Therapeutics for diazoxide choline prolonged-release …
