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BioWorld - Saturday, February 21, 2026
Home » Topics » Drugs » Small molecule

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Going public ticker

Stock skyrockets after Turn goes public

Oct. 9, 2025
By Randy Osborne
No Comments
An uncommon route to the public markets – direct listing – paid off for Turn Therapeutics Inc., with shares (NASDAQ:TTRX) closing Oct. 9 at $9.20, up $2.20, or 31%, having risen as high as $26.50 in its second day of trading. The firm is advancing late-stage clinical programs in eczema and onychomycosis. Also in the works are global health initiatives in thermostable vaccine delivery designed to serve underserved areas.
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Lung illustration

Jascayd nod could set stage for resurgence in IPF drug market

Oct. 8, 2025
By Jennifer Boggs
No Comments
More than a decade after the last idiopathic pulmonary fibrosis (IPF) treatment gained U.S. FDA approval, Boehringer Ingelheim GmbH’s Jascayd (nerandomilast) is set to hit the market following the agency’s green light on Oct. 7. While expected to offer a modest benefit over existing therapies, Jascayd, an orally administered preferential inhibitor of phosphodiesterase 4B with breakthrough therapy status, is viewed by analysts as the first of several potential advancements in the IPF space over the next few years.
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Glass globe with documents and pen

Zenas gets global rights for Innocare BTK inhibitor in $2B+ deal

Oct. 8, 2025
By Lee Landenberger
No Comments
In a deal that could top $2 billion, China-based Innocare Pharma Ltd. licensed the exclusive worldwide development and commercialization rights to the BTK inhibitor orelabrutinib to Zenas Biopharma Inc. for multiple sclerosis and other indications aside from oncology.
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Hand holding thin piece of film

Taho submits US NDA for first apixaban oral dissolving film

Oct. 7, 2025
By Marian (YoonJee) Chu
No Comments
Taho Pharmaceuticals Ltd. announced an NDA submission to the U.S. FDA for TAH-3311, developed as the world’s first oral dissolving film formulation of apixaban, marking a regulatory milestone for the Taipei-based biotech.
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3D dollar sign

Full-Life nabs $77M for radiopharmaceuticals, Belgium GMP site

Oct. 7, 2025
By Marian (YoonJee) Chu
No Comments
Full-Life Technologies Ltd. announced Sept. 29 the completion of a $77 million financing, comprising $50 million in series C equity and $27 million in debt financing, which will be used to advance a portfolio of radiopharmaceuticals and radionuclide-drug conjugates worldwide.
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Person testing glucose level

Biomea’s ‘durable’ menin inhibitor advancing in hard-to-treat diabetes

Oct. 7, 2025
By Karen Carey
No Comments
Among severe insulin-deficient diabetes patients, 12 weeks of 100-mg, once-daily dosing of Biomea Fusion Inc.’s icovamenib lowered hemoglobin A1c by 1.8% from placebo at the 52-week timepoint, an increased benefit over and above what was seen at 26 weeks.
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Art concept for inflamed human tissue
Dermatologic

Arcus Biosciences announces new anti-inflammation programs

Oct. 7, 2025
No Comments
Arcus Biosciences Inc. has announced five new research programs for autoimmune and inflammatory diseases, and is targeting initiation of the first clinical studies next year.
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Musculoskeletal

PRMT6 is key regulator of osteoclast metabolism and fracture repair

Oct. 7, 2025
No Comments
Impaired fracture healing is a clinical management challenge. Fracture healing can be impaired due to several factors, such as aging, chronic inflammation or metabolic abnormalities. Osteoclasts play a crucial role in bone tissue reconstruction, but their abnormal activation can lead to impaired fracture healing. In a recent publication in Frontiers in Immunology, researchers from Naval Military Medical University and collaborators searched for crucial regulatory genes in the process of bone fracture healing.
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Abortion dispute active, FDA clears new generic pill

Oct. 3, 2025
By Randy Osborne
No Comments
With U.S. President Donald Trump’s administration vocally opposed to abortion, the U.S. FDA has approved a new generic version of the pill that makes the procedure possible medically: mifepristone, once better known as RU-486.
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Zepzelca-Tecentriq

Jazz-Roche lung cancer combo approved by FDA

Oct. 3, 2025
By Lee Landenberger
No Comments
The U.S. FDA has approved the priority sNDA for a new first-line maintenance therapy in extensive-stage small-cell lung cancer from Jazz Pharmaceuticals plc. Zepzelca (lurbinectedin) can now be combined with Tecentriq (atezolizumab, Roche AG) or atezolizumab and hyaluronidase-tqjs (Tecentriq Hybreza, Roche) as a maintenance therapy for adults who haven’t progressed after first-line induction therapy with atezolizumab, carboplatin and etoposide.
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