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From siloed data to breakthroughs: multimodal AI in drug discovery

Drug Target Review

Drug development faces significant challenges: long timelines, high costs , complex processes and low probabilities of success (PoS), exacerbated by the shift towards more complex molecules, biologics and cell and gene therapies, hindering patient access to vital treatments. Nature Medicine, 28, 1656–1661 (2022) [link]

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A spatial approach to understanding drug dynamics using mass spectrometry imaging

Drug Target Review

Targeted drug delivery and therapeutic development MSI offers significant advantages for those developing small molecule therapeutics. 2021, 56 (8), e4717. 2021, 32 (4), 977–988. For instance, Cheng et al. Mass Spectrom. Xie F, Gales T, Ringenberg MA, et al. Release 2022, 352 , 199–210. Mass Spectrom.

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A Visual Guide to Gene Delivery

Codon

CAR-T therapy (perhaps the most promising cancer treatment of the last several decades) is one example, in which scientists extract a patient’s blood cells, modify T cells so they can recognize and attack malignancies more effectively, and reinfuse them back into the body.

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Leveraging agonist antibodies to address immunological diseases

Drug Target Review

This targeted enhancement not only boosts the body’s natural mechanisms but also holds promise for developing novel treatments in immunology, where modulating immune responses can lead to more effective and durable therapeutic outcomes. Nat Rev Immunol 21, 680–686 (2021). Therap Adv Gastroenterol. 4 McInnes IB, Gravallese EM.

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Crinecerfont

New Drug Approvals

Formula C 27 H 29 Cl 2 FN 2 OS Crinecerfont , sold under the brand name Crenessity , is a medication used for the treatment of congenital adrenal hyperplasia. [1] Jump up to: a b c d e f g h i j k l m n o p q “FDA Approves New Treatment for Congenital Adrenal Hyperplasia” U.S. 321839-75-2 Molecular Weight 519.50

FDA
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Best-in-Class Solutions Accelerate Development of GLP-1 Therapeutics

PPD

Initially approved for treatment of Type 2 diabetes and later for obesity studies in GLP-1 are now expanding in other indications such as obstructive sleep apnea (OSA), heart failure with preserved ejection fraction (HFpEF) and chronic kidney disease (CKD). It is worth noting that trial ran from 2018 to 2021, before the U.S.

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Hetrombopag Olamine

New Drug Approvals

Hetrombopag olamine (6), an oral nonpeptide thrombopoietin receptor (TpoR)agonistdevelopedby JiangsuHengruiPharmaceutical, was approved in China in June2021 for treatment of adult patients with chronic primary immune thrombocytopenia (ITP) and severe aplastic anemiawhohave not responded well to other treatments.46Hetrombopag,