Lipocine seeks partner for midphase NASH prospect

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Sep 28, 2022

The U.K. drug regulator has told healthcare professionals to exercise caution when considering switching between long-acting attention deficit hyperactivity disorder therapies from companies including Johnson & Johnson, Novartis and Takeda.

After wrapping up a phase 3 trial of its subcutaneous efgartigimod, argenx has submitted the data to the FDA to support a targeted approval in the treatment of generalized myasthenia gravis.

Lipocine has rethought its strategy, focusing on the oral delivery of central nervous system in a pivot that leaves it looking for partners for potential treatments of conditions including nonalcoholic steatohepatitis and cirrhosis.

The Top Line Podcast: don’t miss out on the newest episode where we discuss ASCO data, rising health tech stars, and more. Listen now.

 

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MHRA raises concerns with switching between long-acting J&J, Novartis and Takeda drugs

The U.K. drug regulator has told healthcare professionals to exercise caution when considering switching between long-acting attention-deficit/hyperactivity disorder therapies from companies including Johnson & Johnson, Novartis and Takeda.
 

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This week on "The Top Line," we'll discuss how two Big Pharma companies, GSK and Takeda, made moves this week to bolster their environmental sustainability efforts. We'll discuss their strategies and what we can expect for the future.

 

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