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BioWorld - Thursday, February 12, 2026
Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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SalioGen obtains funding to advance research into genetic therapy for cystic fibrosis

Jan. 7, 2022

Cystic Fibrosis Foundation award supports development of Peptilogics' PLG-0301 and PLG-0206

Jan. 7, 2022
Resp app and sensor

Strados Labs reels in $4.5M for smart respiratory sensor

Jan. 5, 2022
By Catherine Longworth
Investors including SOSV, Cultivate(MD), Wavemaker360 Health, Blu Venture Investors and Broad Street Angels are backing Strados Labs LLC with $4.5 million. The pre-series A funding will be used to accelerate development of the company’s smart sensor platform Resp. The funding comes after Strados received FDA clearance for the product in December 2021 and brings its total raised to $7 million.
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Study shows nanoparticles could help reduce acute lung inflammation in COVID-19

Jan. 5, 2022

Respiratory

Jan. 1, 2022
Woman holding smartphone coughing

Resapp’s stand-alone cough counter app cleared in Australia and Europe

Dec. 29, 2021
By Tamra Sami
PERTH, Australia – Australian digital health company Resapp Health Ltd. received clearance from Australia’s Therapeutics Good Administration and CE mark certification in the EU for its stand-alone cough counter application that tracks cough frequency using a smartphone. The class I software as a medical device is the first regulatory approval for such an application, which uses Resapp’s machine learning algorithms to identify cough events from audio recorded using the smartphone’s in-built microphone.
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Claritas to develop R-107 for persistent pulmonary hypertension of the newborn

Dec. 23, 2021

Chiesi identifies new discoidin domain-containing receptor inhibitors

Dec. 22, 2021

Mesoblast shares depressed by Novartis deal termination

Dec. 21, 2021
By Tamra Sami
PERTH, Australia – It’s been a year that Mesoblast Ltd. might like to forget. The company’s stock dropped 17% Dec. 15 on the news that Novartis AG will terminate its licensing agreement with Mesoblast for remestemcel-L.
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Sanofi/Regeneron’s asthma blockbuster Dupixent has new rival as FDA approves Astrazeneca/Amgen’s Tezspire

Dec. 20, 2021
By Richard Staines
The FDA has approved Astrazeneca plc and Amgen Inc.’s first-in-class biologic, tezepelumab, for the add-on maintenance treatment of adults and children ages 12 and older with severe asthma, adding further competition to a hotly contested market. An injection marketed under the brand name Tezspire, tezepelumab inhibits the action of thymic stromal lymphopoietin (anti-TLSP). This is a signaling molecule at the top of several cascades influencing allergic, eosinophilic and other types of airway inflammation associated with severe asthma, including airway hyperresponsiveness.
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