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PTC inks Royalty deal worth up to $1.5B on Genentech-partnered SMA drug Evrydsi

Fierce Pharma

The company licensed the med to Genentech in 2011. Amid a cost-cutting drive and a looming commercial threat in Europe, PTC Ther | PTC will hold on to 19% of its royalty interest in the Genentech drug with the option to sell the rest down the line.

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Biotech IPO market slowdown continues as third quarter is weakest since 2011

MedCity News

Third Harmonic Bio’s stock market debut was the only biotech IPO that crossed the $100 million threshold in the third quarter as the slowdown in IPO activity showed little sign of changing. Small deals continue to represent most of the IPO activity.

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Thursday pharma headlines

World of DTC Marketing

regulators knew about reports of suicidal behavior in men taking the anti-baldness treatment Propecia when they decided not to warn consumers of those potential risks in a 2011 update of the popular drug’s label. This week I had a long talk with someone who has been working in pharma R&D for over 30 years about Covid vaccines.

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The Caregiver Vertical: How Pharma Engages

Pharma Marketing Network

5 While the CDC gathers information on these topics for public health planning, there are immediate needs that pharma can address. . What Can Pharma Do? Including caregiver insights and creating specific caregiver materials in the product development cycle is a good place for pharma to engage caregivers. Sunny White.

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New regulatory relief to benefit Europe’s pharma SMEs

European Pharmaceutical Review

The new rules will repeal the 2011 Directive on late payments and will replace it with a Regulation. The post New regulatory relief to benefit Europe’s pharma SMEs appeared first on European Pharmaceutical Review. This is compared to 1.8 percent for large enterprises, which is lower than its 2019 level.

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FDA Finally Pulls Preterm Birth Drug Makena From the Market

MedCity News

FDA withdrawal of Makena from the market comes four years after the drug, granted accelerated approval in 2011, failed a post-marketing study to confirm the drug’s benefit. The FDA decision also affects generic versions of the drug.

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Leading in Pharma: a woman’s pathway

European Pharmaceutical Review

To mark International Women’s Day, EPR talked to Dr Ekaterina Malievskaia, Chief Innovation Officer and Co-founder of COMPASS Pathways about her inspiration, the challenges as a woman working in pharma and advice for women entering the industry. What challenges have you faced as a woman in pharma?

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