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BioWorld - Wednesday, May 6, 2026
Home » Topics » Drugs » Small molecule

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FDA Approved stamp with pills

Sun Pharma’s JAK inhibitor for severe alopecia gets US FDA nod

July 30, 2024
By Lee Landenberger
The U.S. FDA has approved Sun Pharmaceutical Industries Ltd.’s Leqselvi (deuruxolitinib), a JAK1 and JAK2 inhibitor for adults with severe alopecia areata, a chronic autoimmune disease. The twice-daily, oral treatment will be targeting a company-estimated market of about 300,000 people in the U.S. This is the third FDA-approved treatment for severe alopecia areata in the past three years.
Read More
Immune checkpoint inhibitors illustration of PD-1, CTLA-4 and PD-L1.

Boehringer buying Nerio for $1.3B for checkpoint inhibitors

July 30, 2024
By Lee Landenberger
The dealmaking continues at Boehringer Ingelheim GmbH as it plans to buy Nerio Therapeutics Inc. for $1.3 billion. The German company is bolstering its cancer programs with the Nerio acquisition, which will be added to multibillion-dollar deals cut earlier this year for cancer immunotherapies and nonalcoholic or metabolic dysfunction-associated steatohepatitis (NASH/MASH) treatments.
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Test tube, dropper, DNA illustration
Endocrine/metabolic

BI-9787 made available for metabolic disorder studies

July 30, 2024
Scientists at Boehringer Ingelheim GmbH have made the ketohexokinase (KHK) inhibitor BI-9787 freely available as a tool compound via the company’s Opnme program.
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Drug R&D concept image.
Neurology/psychiatric

Novel articaine derivative has improved anesthetic, anti-inflammatory properties

July 30, 2024
DeepSA, an edit-based generative framework that utilizes deep simulated annealing (SA), was used to develop novel local anesthetics with multiple activities. Researchers from Sichuan University applied DeepSA to generate over 400 analogs of the local anesthetic articaine.
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Scientific illustration of a migrating breast cancer cell
Cancer

HDAC inhibitor prevents breast cancer metastasis

July 30, 2024
Researchers from Northeast Normal University in Changchun demonstrated that compound AW-01178 reversed the abnormal regulation of E-cadherin by inhibiting the class I HDAC enzyme.
Read More
Coins and seedling
Newco news

Draupnir engaging sortilin receptor with €12M seed round

July 29, 2024
By Nuala Moran
Draupnir Bio is poised to advance a new approach to targeted protein degradation by engaging the sortilin receptor on lysosomes to promote the destruction of extracellular and membrane-bound disease proteins.
Read More
Elderly hands holding broken brain structure

Despite endpoint miss, Cognition sees path forward in Alzheimer’s

July 29, 2024
By Jennifer Boggs
Cognition Therapeutics Inc. said it is moving to the next stage of clinical testing with oral, small-molecule candidate CT-1812, despite phase II efficacy results falling short of statistical significance in patients with mild to moderate Alzheimer’s disease and sending shares of the Purchase, N.Y.-based company (NASDAQ:CGTX) falling 44%, or $1.04, to close July 29 at $1.33.
Read More
Hands holding holographic intestine
Newco news

Ensho debuts to target gut inflammation with oral α4β7 inhibitors

July 26, 2024
By Marian (YoonJee) Chu
Ensho Therapeutics Inc. launched in July after licensing a pipeline of four oral α4β7 inhibitors for inflammatory and gastrointestinal disorders, including inflammatory bowel disease (IBD), from EA Pharma Co. Ltd. “Millions of people worldwide are living with IBD,” Ensho founder, president and executive chair Neena Bitritto-Garg recently told BioWorld, “and while there are a number of approved medications to address the symptoms of IBD, it remains a difficult-to-treat disease with high relapse rates for a considerable proportion of patients.”
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From Day One, Ipsen gains ex-US rights to tovorafenib for $461M

July 26, 2024
By Marian (YoonJee) Chu
Ipsen SA, of Paris, struck a $461 million deal with Day One Biopharmaceuticals Inc. for ex-U.S. rights to tovorafenib, an oral drug for pediatric brain tumor that gained U.S. FDA accelerated approval April 23 as Ojemda (tovorafenib).
Read More
FDA Approved stamp with pills

Sun Pharma’s JAK inhibitor for severe alopecia gets US FDA nod

July 26, 2024
By Lee Landenberger
The U.S. FDA has approved Sun Pharmaceutical Industries Ltd.’s Leqselvi (deuruxolitinib), a JAK1 and JAK2 inhibitor for adults with severe alopecia areata, a chronic autoimmune disease. The twice-daily, oral treatment will be targeting a company-estimated market of about 300,000 people in the U.S. This is the third FDA-approved treatment for severe alopecia areata in the past three years.
Read More
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