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Actithera draws new investors to radiopharma drug pitch

BioPharma Drive: Drug Pricing

in 2013 — the field has taken off since the success of Novartis’ prostate cancer treatment Pluvicto. The technology works by attaching a radioisotope to a targeting compound via a specially engineered “linker” molecule. While radiopharmaceuticals have been around for years — Bayer’s Xofigo was approved in the U.S.

Drugs 155
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David Liu receives Breakthrough Prize in Life Sciences

Broad Institute

In 2013, Broad founding director Eric S. Since its founding in 2013 by Sergey Brin, Priscilla Chan and Mark Zuckerberg, Yuri and Julia Milner, and Anne Wojcicki, the Breakthrough Prize has been given to standout individuals in life sciences, mathematics, and fundamental physics. Lander was among the inaugural recipients of the prize.

Science 144
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Designing antibodies to think before they bind

Drug Target Review

Meet Jhong-Jhe (JJ) You JJ joined AP Biosciences in 2013 as the company’s first employee, leading the development of the Omni-Mab human antibody phage display library and building a robust cell-based assay platform for screening and isolating functional antibodies for immunotherapy.

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Protein degraders: chasing undruggable targets

BioPharma Drive: Drug Pricing

Since Crews launched Arvinas in 2013, various biotechs have set out with their own spins on the idea, chasing different degrader pathways to the lysosome or proteasome. Cacace, of Arvinas, said those discoveries were “key pieces” that helped companies “bridge to greater tools” and led to oral drug-like molecules. "It

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Labuxtinib

New Drug Approvals

Compound 1 can be prepared according to example Fl 10 of WO 2013/033070 Al, which is incorporated by reference herein, as summarized in the Scheme 1 provided below: Scheme 1. 2013-03-07. Compound 1 [0022] As defined above, a pharmaceutical composition of the present invention is a micronized powder comprising Compound 1.

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Vamorolone

New Drug Approvals

The synthesis is disclosed in Bioorganic & Medicinal Chemistry, Volume 21 , Issue 8, 15 April 2013, Pages 2241-2249. 21 (2013) 2241–2249. 2013, 21, 2241− 2249. 2013, 21, 2241−2249. 21 (2013) 2241–2249 Nat. Reeves EK, Hoffman EP, Nagaraju K, Damsker JM, McCall JM (April 2013). October 2013).

FDA 62
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Gene editing extends lifespan in mouse model of prion disease

Broad Institute

Not long after the development of CRISPR-Cas9 gene editing in 2013, Vallabh and Minikel began thinking about whether CRISPR could be used to disrupt the gene encoding the prion protein. The wife-and-husband team started a lab at the Broad with a singular focus: preventing and treating prion disease within their lifetime.

Disease 144