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Home » Newsletters » BioWorld

BioWorld

April 22, 2021

View Archived Issues
FDA-approved-stamp6.png

Anaptysbio’s GSK-partnered dostarlimab finally gets FDA nod after pandemic delay

Another PD-1 antibody is about to hit the U.S. market, following the FDA’s accelerated approval of dostarlimab (TSR-042) from partners Anaptysbio Inc. and Glaxosmithkline plc. But dostarlimab, branded Jemperli, will be only one of two PD-1 drugs indicated for endometrial cancer, going up against Merck & Co. Inc.’s Keytruda (pembrolizumab). Read More

Like a rock: Obsidian and Vertex enter a gene editing deal worth up to $1.3B

After cutting a deal worth up to $1.1 billion with Crispr Therapeutics AG, it took Vertex Pharmaceuticals Inc. only two days to come up with another collaboration that could top the $1 billion mark, this time with Obsidian Therapeutics Inc. Read More
R&D money

Foreign interference in U.S. biomedical research a costly enterprise

As of 2020, the NIH had identified 507 grant recipients who potentially had undisclosed conflicts of interest, with many of those conflicts involving affiliations with foreign governments that may expect the scientists to share or steal NIH-funded research. Read More

CRISPR bakin’: Intellia on sizzle as Wall Street crunches available data

Advances lately in the genome-editing space include Beam Therapeutics Inc. publication in The CRISPR Journal details of its work with inlaid base editors, which the firm is applying in the BEAM-102 program for sickle cell disease. IBEs’ predictable, shifted editing window lets researchers go after disease-causing mutations that canonical base editors cannot reach, Beam said, and do the job with high efficiency and few off-target effects on the genome. The hottest news due in the near-term future from the sector will spill from Intellia Therapeutics Inc., of Cambridge, Mass., which is due to roll out first-in-human data with a systemic CRISPR-based genome editing therapy, NTLA-2001, in hereditary transthyretin amyloidosis. Read More
Gastric cancer

ITM raises the roof with $108M convertible loan for radiopharmaceutical pipeline

DUBLIN – Isotopen Technologien München (ITM) AG raised €90 million (US$108 million) in debt financing to complete phase III development of its lead radiopharmaceutical, solucin, in gastroenteropancreatic-neuroendocrine tumors and to take forward several more preclinical pipeline projects. Read More

Anavo Therapeutics closes $24M seed round to drug the phosphatome

DUBLIN – Anavo Therapeutics BV raised €20 million (US$24 million) in seed financing to fund the build-out of a platform that aims to drug the human phosphatome, or the ensemble of phosphatase enzymes that plays a crucial role in maintaining cells’ phosphorylation balance by removing phosphate groups from their target substrates. Read More

PCSK9 affects antitumor immunity

The enzyme proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a major role in the regulation of blood LDL cholesterol levels. Now, new research shows that targeting PCSK9 may also potentiate checkpoint blockade. Read More

Autophagy chaperone targets aggregation-prone proteins

BioWorld looks at translational medicine, including: Pharmacological target for anorexia. Read More

Appointments and advancements for April 22, 2021

New hires and promotions in the biopharma industry, including: Eiger, HMNC Brain Health, Lumen, Neonmind, Nervgen, Sutro. Read More

Financings for April 22, 2021

Biopharmas raising money in public or private financings, including: Aikido, Austrianova, Centessa, Evolus, Neubase, Pep-Therapy. Read More

In the clinic for April 22, 2021

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Advita, Alladapt, Candel, Can-Fite, Chimeric, Delpor, Genethon, Hoth, Karolinska, Lipidor, Mediwound, Monopteros, Onconova, Organicell, Ortho Dermatologics, Pharming, Protokinetix, Relief, SAB, Shanghai Junshi, Umecrine, Valneva, Yumanity, Zogenix. Read More

Regulatory actions for April 22, 2021

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Amarin, Henlius, Saniona, Ultragenyx. Read More

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