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Antibody Drug Conjugates: windows of opportunity

Drug Target Review

These therapies have broadened treatment options for patients to expand beyond the more traditional small molecule drug alternatives. The global ADC market is expected to continue this steep upward trajectory and is anticipated to exceed $16 Billion by 2026. 3D rendering of Antibody Drug Conjugate Molecules.

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Boehringer Ingelheim and German Chancellor Olaf Scholz lay the foundation stone for the 285 million EUR innovation center

The Pharma Data

Starting in 2026, this facility will develop manufacturing processes for active pharmaceutical ingredients and produce drugs for use in clinical trial phases. Biopharmaceuticals and small molecules each account for approximately half of the company’s research pipeline.

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Lessons From A Private Funding Round: Science, Relationships, And Experience

LifeSciVC

We experienced strong enthusiasm for small molecule research in the investor community. We have milestones on the horizon, and we want investors to stay close to the Sionna story even if we don’t need capital until 2026. The last takeaway is just how much the experience around us made a difference.

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Advancing regenerative cell therapy development

Drug Target Review

This is in part due to a complex manufacturing process, which is harder to control than those used for other modalities (such as small molecules and monoclonal antibodies). Then it’s on to dosing and administration studies in animals, pivotal toxicology studies, and, following a successful funding round, first-in-human studies in 2026.

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Fujifilm to Invest Over 200 Billion yen (2 Billion USD) to Establish New Large-Scale Cell Culture Manufacturing Site for Biopharmaceuticals in the U.S.A.

The Pharma Data

Beyond fiscal year ending March 2026 , Fujifilm expects this latest investment to boost the annual growth rate of its Bio CDMO Business to 20%, greatly exceeding market projections. Bio-CDMO business offers services for biopharmaceuticals and small molecule pharmaceuticals. Overview of New Site.

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Analysis Life Sciences Thank You FDA’s new guidance on postapproval manufacturing changes for biosimilars focuses on current practice, new dosage forms

Agency IQ

in equipment) for products that are more complex or aren’t as well-characterized, such as antibody drug conjugates or recombinant DNA products, will be considered higher risk than they would if the change was made to the production of standard, small molecule products. Any CMC changes (e.g., Comments are due September 23, 2024.

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AstraZeneca to Acquire Alexion, Accelerating the Company’s Strategic and Financial Development

The Pharma Data

AstraZeneca has developed a broad range of technologies, initially focused on small molecules and biologics and with a growing focus in precision medicine, genomics, oligonucleotides and epigenetics. 2 EvaluatePharma, World Preview 2020, Outlook to 2026. AstraZeneca PLC. _. This announcement contains inside information.