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Boehringer Ingelheim shares updated 2030 environmental sustainability commitments

The Pharma Data

At Boehringer Ingelheim, making our planet healthier is an integral part of our purpose to pioneer breakthrough therapies that transform the lives of humans and animals for generations. Boehringer Ingelheim Boehringer Ingelheim is working on breakthrough therapies that improve the lives of humans and animals.

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How to Successfully Prepare for the HTAR Implementation in the EU

thought leadership

The HTAR will take effect in January 2025 for oncology and/or advanced therapy medicinal product (ATMP) therapies, with other therapies following a staggered implementation process, including orphan drugs in 2028 and all drugs in 2030.

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Sentiment & Themes Emerging From JPM 2024

LifeSciVC

These are incredible forecasts and CAGRs, which if we assume directionally correct, rely not only on steady growth for approved therapies but also a substantial success rate of, and continued investment in, the development pipeline. recent announcements from Merck and Sanofi for obesity and broader metabolic disease).

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Development of Blood-Based Alzheimer’s Prognostic Propels Diadem to Finalist Status for Both the Gaetano Marzotto Company Prize and 2030 Social Impact Special Prize

The Pharma Data

16, 2020 /PRNewswire/ — Diadem srl , a company developing the first blood-based test for the prediction of early onset Alzheimer’s disease, today announced that it has been selected as a finalist for both the Gaetano Marzotto Company Prize and the Gaetano Marzotto 2030 Social Impact Special Prize. . MILAN , Nov.

Disease 40
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How organoids can redefine pre-clinical research

Drug Target Review

Organoid technologies are becoming an invaluable solution for preclinical research, with the ability to augment the development of personalised medicine, drug discovery and gene therapies. billion by 2030. Organoids for cell therapy and drug discovery. Cell Stem Cell [Internet]. 2023 May;30(5):571–91. Elsevier; 2020.

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Roche’s anti-amyloid beta antibody gantenerumab granted FDA Breakthrough Therapy Designation in Alzheimer’s disease

The Pharma Data

Roche announced that gantenerumab, an anti-amyloid beta antibody developed for subcutaneous administration, has been granted Breakthrough Therapy Designation by the U.S. This designation for gantenerumab marks the 39th Breakthrough Therapy Designation for Roche’s portfolio of medicines. trillion per year by 2030.

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Investment Trends in Pharmaceutical Research

DrugBank

In 2021, an estimated 537 million adults were living with diabetes, a number projected to reach 643 million by 2030. billion by 2030. These new therapies have demonstrated significant LDL cholesterol reductions, but their high cost remains a barrier to widespread adoption. The market for cardiovascular drugs, valued at 155.6