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Risk adjusted net present value: What is the current valuation of Eli Lilly and Co’s Retatrutide?

Pharmaceutical Technology

According to Globaldata, it is involved in 10 clinical trials, of which 4 were completed, 5 are ongoing, and 1 is planned. GlobalData uses proprietary data and analytics to provide a complete picture of Retatrutide’s valuation in its risk-adjusted NPV model (rNPV). It is a new molecular entity. million in FY2021.

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Risk adjusted net present value: What is the current valuation of Novartis’s Gevokizumab?

Pharmaceutical Technology

According to Globaldata, it is involved in 34 clinical trials, of which 20 were completed, 1 is ongoing, and 13 were terminated. GlobalData uses proprietary data and analytics to provide a complete picture of Gevokizumab’s valuation in its risk-adjusted NPV model (rNPV). It is a new molecular entity (NME).

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Femtech in 2023: Covid-19 spurs interest in digital solutions

Pharmaceutical Technology

But while the pandemic hampered access to health care services, it also led to accelerated demand for digital health technologies that enabled women to access remote care during lockdowns, said Wafaa Hasan, GlobalData’s healthcare analyst at a Femtech-centric webinar held on March 30.

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Pharma’s ESG goals need to underscore push for health equity

Pharmaceutical Technology

On October 6, in a GlobalData webinar, experts tried to answer the question ‘ Is Pharma at an ESG turning point?’ , revealing a multitude of diverse strategies for pharmaceutical companies to remain conscious of their global impacts. GlobalData is the parent company of Pharmaceutical Technology.

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Challenges and opportunities in the CGT supply chain

European Pharmaceutical Review

A recent survey 1 of healthcare industry professionals showed that CGT is expected to have the most significant impact on the pharmaceutical industry in 2024. The CGT supply chain presents unique challenges, from regulatory compliance and temperature and time control to customs clearance and security. Internet] GlobalData.

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Excitement associated with FDA approval of Rinvoq in Crohn’s disease

Pharmaceutical Technology

Rinvoq is expected to have a rapid uptake in the CD market by healthcare providers (HCPs) due to the overall positive sentiment associated with this therapy.

FDA 52
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Lupkynis approved for the treatment of LN in the EU and UK

Pharmaceutical Technology

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has also since granted the Great Britain marketing authorisation of Lupkynis to treat adults with active LN. Notably, Lupkynis is the first oral therapy approved by the US Food and Drug Administration (FDA) and EC for the treatment of active LN.