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MASH innovator drug partnerships surge over $2.5 bn in 2024YTD: GlobalData

Express Pharma

Biopharmaceutical companies are regaining interest in metabolic dysfunction-associated steatohepatitis (MASH) innovator drug development. MASH innovator drugs witnessed over $2.5 GlobalData’s Pharma Intelligence Center Deals Database reveals that MASH drugs secured over $5.7

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Alimera Sciences buys US rights to EyePoint’s Yutiq

Pharmaceutical Technology

It received approval from the US Food and Drug Administration in October 2018. Yutiq is indicated to treat chronic, non-infectious uveitis that affects the posterior segment of the eye.

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Novo Nordisk’s gene silencing alliance with Dicerna bears first fruit

pharmaphorum

million – including $175 million upfront and an equity investment of $50 million – to find multiple RNA interference (RNAi) candidates for diseases like non-alcoholic steatohepatitis (NASH) and type 2 diabetes. The nomination of a first candidate in the collaboration that will advance into development triggers a $2.5

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Gene therapy: a radical pharmaceutical revolution

European Pharmaceutical Review

In this Q&A, Karen Pinachyan, Head of Medical Affairs Europe at CSL Behring summarises key considerations for gene therapy drug development and the ideal approach for alleviating economic strain when advancing these modern treatments. 4,5 What is the key consideration drug developers should apply to gene therapies?

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Is India capable of ensuring equitable access to biopharmaceuticals?

Express Pharma

According to the World Health Organisation (WHO), an estimated two billion people across the world do not have access to essential medicines for life threatening diseases like cancer, AIDS and even autoimmune diseases like Type 1 diabetes.

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Drug Repurposing: Unlocking access to rare solutions

Express Pharma

In the marathon of drug development, where billions of dollars and over a decade of research are the norm, drug repurposing is quietly reshaping the landscape. Challenges in drug repurposing Despite these technological and regulatory advancements, the journey of drug repurposing is not without its challenges.

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USP standards build trust in biologics and biosimilars

Quality Matters

Novel biologics and biosimilars – or biologics highly similar to an existing biologic already approved – also hold great promise to help increase availability of quality biologic medicines for conditions ranging from diabetes to cancer. Another example is mRNA vaccines.