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Novaliq’s dry eye disease therapy receives US FDA approval

Pharmaceutical Technology

Novaliq medical science and regulatory affairs vice-president Sonja Krösser stated: “We are proud that the FDA approved VEVYE. The safety and efficacy of VEVYE were assessed in a total of 1,369 patients with dry eye disease, of which 738 received VEVYE.

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Dapagliflozin approved for heart failure across LVEFs

European Pharmaceutical Review

“Dapagliflozin has been clinically shown to reduce hospitalisations and cardiovascular deaths in heart failure,” commented Dr John McMurray, Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, UK. “[The] Overall, serious AEs, including death, were reported in 43.5

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It’s Time We Got the Most Out of Medical Affairs Data

PM360

Field Medical Affairs is an essential bridge between pharmaceutical clinical development and commercial delivery. Historically, the industry has left MSL-HCP interactions to exist on their own, focusing on objective metrics and key performance indicators (KPIs) to inform Medical Affairs impact.

Medical 52
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Leveraging innate cell engagers for lymphoma treatment

European Pharmaceutical Review

These efficacy results, combined with the safety profile that allows patients to complete their treatment regimen, are extremely encouraging. The majority of patients experienced only mild to moderate treatment-related adverse events, confirming a well-manageable safety profile. later acquired by Eli Lilly and Company.

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How to Become a Pharmaceutical Sales Representative

Pharmaceutical Representative Training

Pharmacology is the science of medications and the role they play in the body. Being able to describe a drug’s mechanism of action (how it works), its efficacy (how effective it is) and its safety profile, are important to providing HCPs with a fair, balanced message. Pharma Sales Rep Salary & Perks.

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Why R&D innovation holds the key to greater patient impact

European Pharmaceutical Review

By collaborating with several stakeholders and authorities, multiple stages of development can take place concurrently to speed up R&D without compromising safety protocols. Previously, he spent more than 10 years at Roche in multiple positions within medical affairs. The COVID-19 blueprint has shown a way forward.

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What Tech Trends Do Life Sciences Marketers Need to Know About?

PM360

Casey Cronin Life sciences marketers have a unique opportunity to connect with target audiences on an individual level and foster brand safety through AI advancement. Will Big Tech’s moves within healthcare force the industry to change how it operates? Here are the best responses.