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BioWorld - Tuesday, April 14, 2026
Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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Respiratory

Genentech patents new LATS1 and/or LATS2 inhibitors for ARDS

Jan. 3, 2023
Genentech Inc. has disclosed 2,8-diazaspiro [4.5] decane compounds acting as serine/threonine-protein kinase LATS1 and/or LATS2 inhibitors reported to be useful for the treatment of acute respiratory distress syndrome (ARDS).
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Xenoview in lungs in MRI

Polarean Imaging wins FDA nod for hyperpolarized MRI contrast agent

Dec. 30, 2022
By Meg Bryant
The U.S. FDA has approved Polarean Imaging plc’s drug-device combination product, Xenoview, for use with magnetic resonance imaging (MRI) in evaluating lung ventilation in adults and children aged 12 and older. The hyperpolarized contrast agent, which is prepared from the Xenon Xe 129 gas blend, is expected to be commercially available in the U.S. starting next month.
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Respiratory

Azcuris reports development of TSLP/TSLPR interaction inhibitors

Dec. 29, 2022
Research at Azcuris Co. Ltd. has led to the development of thymic stromal lymphopoietin (TSLP)/cytokine receptor-like factor 2 (CRLF2; TSLPR) interaction inhibitors, which are reported to be useful for the treatment of autoimmune diseases, chronic obstructive pulmonary disease (COPD), allergy, asthma, allergic rhinitis and chronic rhinosinusitis.
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Respiratory

NLRP3 inflammasome inhibitors described in Roche patent

Dec. 29, 2022
F. Hoffmann-La Roche Ltd. and Hoffmann-La Roche Inc. have described NLRP3 inflammasome inhibitors reported to be useful for the treatment of asthma and chronic obstructive pulmonary disease (COPD).
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Colorized scanning electron micrograph of human respiratory syncytial virus.
Infection

Poolbeg's collaboration with Onethree Biotech identifies potential RSV drug candidates

Dec. 22, 2022
Poolbeg Pharma plc has identified potential new drug candidates from its respiratory syncytial virus (RSV) artificial intelligence (AI) program with Onethree Biotech Inc.
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The two phase IIIs of Verona: more positive data prompts NDA talk

Dec. 20, 2022
By Lee Landenberger
After posting positive top-line data in August from its phase III ENHANCE-2 study of ensifentrine for treating chronic obstructive pulmonary disease (COPD), Verona Pharma plc now has positive results from the companion phase III study. The ENHANCE-1 trial of ensifentrine as a COPD maintenance treatment hit its primary and key secondary endpoints, prompting the company to say it plans to submit an NDA for the treatment to the U.S. FDA sometime in the first half of 2023.
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US enforcement for medical testing to remain dangerously robust in 2023

Dec. 20, 2022
By Mark McCarty
U.S. federal authorities have made a lot of noise over inappropriate medical testing in the past two years, largely due to the COVID-19 pandemic, but Paul Garcia, a partner in the San Diego office of Hooper, Lundy & Bookman PC, says this trend will not ebb at all in the coming year. Garcia told BioWorld that the lookback period for Medicare testing claims runs several years and that not only will enforcement results continue to surface next year, but also that the associated civil monetary penalties could force a testing lab to shutter its operations permanently.
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Respiratory

Discovery of a novel CB2 receptor agonist, YX-2102, with promising activity in models of PF

Dec. 20, 2022
Investigators from Army Medical University reported the discovery and preclinical characterization of a novel cannabinoid receptor 2 (CB2 receptor) agonist, YX-2102, being developed as a potential therapeutic candidate for alleviating lung fibrosis.
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Respiratory

Roche discovers new PDK1 inhibitors

Dec. 15, 2022
Roche has synthesized pyruvate dehydrogenase kinase 1 (PDK1) inhibitors reported to be useful for the treatment of systemic lupus erythematosus, psoriasis, inflammatory bowel diseases, idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease and cancer.
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Respiratory

Vertex cleared to enter clinic with mRNA therapy VX-522 for cystic fibrosis

Dec. 13, 2022
Vertex Pharmaceuticals Inc. has received clearance from the FDA for its IND application for VX-522, a messenger ribonucleic acid (mRNA) therapy targeted at treating the underlying cause of cystic fibrosis (CF).
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