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BioWorld - Saturday, January 10, 2026
Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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New CFTR modulators discovered at AbbVie

Aug. 8, 2022
AbbVie has patented cystic fibrosis transmembrane conductance regulator (CFTR) (deltaF508 mutant) correctors reported to be useful for the treatment of cystic fibrosis.
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Lungs wireframe illustration

FDA clears Adherium’s Hailie sensor for GSK’s Ellipta inhaler

Aug. 5, 2022
By Tamra Sami
The FDA granted Adherium Ltd. 510(k) clearance for its next-generation Hailie sensor that connects with Glaxosmithkline plc’s Ellipta inhaler to enable monitoring of medication use for asthma and chronic obstructive pulmonary disorder (COPD).
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Businesswoman pressing dollar sign on touchscreen

Structure Therapeutics nets $33M in financing for GPCR candidates

Aug. 5, 2022
By Doris Yu
Structure Therapeutics Inc. raised $33 million in a financing round to speed up clinical trials of its lead assets targeting chronic diseases and to improve its technology platform. Previously known as Shouti Inc., the company also has rebranded itself as Structure to “reflect its foundation in structural biology and computational design.”
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APT-101 demonstrates efficacy in model of lung injury and fibrosis

Aug. 5, 2022
Researchers from APIE Therapeutics presented preclinical data for the novel apelin receptor (APJ) agonist, APT-101, being developed as a small-molecule antifibrotic and anti-inflammatory agent.
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Kiniksa gets $100M up front from Genentech for monoclonal antibody

Aug. 3, 2022
By Lee Landenberger
Genentech Inc. is paying Kiniksa Pharmaceuticals Ltd. $100 million in up-front and near-term payments for the development and commercialization rights to vixarelimab, a fully human monoclonal antibody. Kiniksa also could receive up to approximately $600 million in certain clinical, regulatory and sales-based milestones, as well as royalties on annual net sales.
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Impact Biomedical announces development of Quantum antihistamine

July 27, 2022
Lung illustration

Mutation-specific targeting increases transporter protein in cystic fibrosis

July 20, 2022
By Mar de Miguel
A study published in Nature Communications revealed a new antisense oligonucleotide therapy applicable to the W1282X mutation of the cystic fibrosis transmembrane conductance regulator gene in cystic fibrosis.
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Mutation-specific targeting increases transporter protein in cystic fibrosis

July 20, 2022

Sunshine Lake Pharma patents new chymotrypsin inhibitors

July 18, 2022
Internal organs: lungs, heart, stomach, diaphragm

Stimdia nets $16M to trial neurostimulation device

July 15, 2022
By Catherine Longworth
Investors are backing neurostimulation device company Stimdia Medical Inc. with $16 million, in the first tranche of a series B offering expected to total $30 million. The Minneapolis-based company is developing a device that stimulates the phrenic nerves in a patient’s neck to exercise the diaphragm during mechanical ventilation and minimize ventilation-induced diaphragmatic dysfunction (VIDD).
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