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BioWorld - Saturday, January 10, 2026
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Female healthcare professional holding dollar sign
Healing the health divide

Despite women’s health inroads, lackluster funding impedes progress

Nov. 14, 2024
By Karen Carey
While women make up half the world’s population and own two out of every five businesses, there are substantial knowledge gaps about conditions affecting their health – mostly due to decades of research excluding women from clinical trials and investment decisions.
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Green strand of DNA

PRV sweetens PTC approval of Kebilidi in AADC deficiency

Nov. 14, 2024
By Randy Osborne
PTC Therapeutics Inc.’s accelerated go-ahead from the U.S. FDA for Kebilidi (eladocagene exuparvovec-tneq), a recombinant adeno-associated virus serotype 2-based gene therapy to treat aromatic L-amino acid decarboxylase (AADC) deficiency, came with a priority review voucher (PRV) that the company intends to monetize.
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Eko Health Low EF Stethoscope

CPT code just the start of Eko’s coverage push for Sensora

Nov. 14, 2024
By Mark McCarty
Eko Health Inc. recently won a category III CPT code for its Sensora platform for cardiovascular disease detection. While a “cat III” CPT code hasn’t traditionally excited industry, the company is convinced that payers will respond because of the massive costs associated with cardiovascular disease.
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Liver over digital lens background

Organox and Egenesis sign agreement for liver support system

Nov. 14, 2024
By Shani Alexander
Organox Ltd. and Egenesis Inc. signed an agreement to advance a liver support system to facilitate liver recovery in the acute setting.
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Cancer cells under magnifying glass

Another TCR T-cell win as Adaptimmune focuses on rare sarcomas

Nov. 13, 2024
By Jennifer Boggs
On the heels of U.S. FDA approval of its first T-cell therapy, Adaptimmune Therapeutics plc reported positive results from a pivotal study for its second candidate, letetresgene autoleucel, expected to support a rolling BLA submission in 2025 that could bolster the firm’s offerings as it narrows its focus on the rare sarcoma space.
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Daiichi Sankyo, Astrazeneca submit new BLA for Trop2 lung cancer ADC

Nov. 13, 2024
By Tamra Sami
Daiichi Sankyo Co. Ltd. and Astrazeneca plc have submitted a new BLA to the U.S. FDA for accelerated approval for datopotamab deruxtecan for treating locally advanced or metastatic epidermal growth factor receptor-mutated non-small-cell lung cancer patients who have received prior systemic therapies.
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Concept of business partnership

Apollo signs near-$1B deal for Sunshine’s FGF21/GLP-1 injection

Nov. 13, 2024
By Marian (YoonJee) Chu
Apollo Therapeutics Group Ltd. and Sunshine Lake Pharma Co. Ltd. inked a potential $938 million licensing deal for APL-18881 (HEC-88473), Sunshine’s dual fibroblast growth factor 21 (FGF21)/glucagon-like peptide-1 (GLP-1) receptor agonist currently in a phase II study for type 2 diabetes.
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Da Vinci Xi robot - Intuitive Surgical

J&J’s Ottava robotic system approved for US pivotal trial

Nov. 13, 2024
By Annette Boyle
Johnson & Johnson received U.S. FDA investigational device exemption to begin the pivotal clinical trial for the Ottava robotic surgical system. If the trial goes well, Ottava could pose a significant challenge to decades-long dominance of the robotic surgical market by Intuitive Surgical Inc.’s Da Vinci system.
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3D illustration of transparent human torso with close up of spinal cord

Nevro wins CE mark for spinal cord stimulation technology

Nov. 13, 2024
By Shani Alexander
Nevro Corp. received CE mark certification for its HFX iQ spinal cord stimulation system that delivers pain relief.
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Cleerly Labs product suite

Cleerly scores win with four-MAC coverage of AI-QCT

Nov. 13, 2024
By Mark McCarty
Device makers are not necessarily fond of the need to acquire Medicare coverage by picking off one Medicare administrative contractor at a time, but Cleerly Labs Inc. worked this path with gusto.
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