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BioWorld - Tuesday, June 16, 2026
Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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Cynata receives ethics approval for MEND study of Cymerus MSCs in COVID-19

May 11, 2020

FDA approves IND for Organicell Flow as treatment of SARS due to COVID-19

May 8, 2020
Athersys researchers standing next to bioreactor in the lab

Pass the MUST-ARDS: Athersys starts pivotal study for stem cells to treat COVID-19-induced ARDS

May 6, 2020
By Stacy Lawrence
Stem cells haven’t exactly panned out as hoped when it comes to approved therapeutics. There are only a couple that have received a nod from the FDA in very specific indications. But the ongoing COVID-19 pandemic could push stem cells back into the limelight and more firmly establish them as therapeutically relevant.
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Enrollment on track in phase IIb GALACTIC-1 study of GB-0139 in IPF

May 6, 2020

Heptares Therapeutics presents new histamine H4 receptor antagonists

May 6, 2020

First patients enrolled in pivotal MACOVIA study of MultiStem in COVID-19-induced ARDS

May 6, 2020
Illustration of Zephyr valve deployment in lung

After scrapped IPO, Pulmonx raises $66M to back minimally invasive emphysema valve

May 5, 2020
By Stacy Lawrence
Chronic obstructive pulmonary disease (COPD) is one of the most dangerous comorbidities for COVID-19 patients – as well as a major cause of death that predates the current pandemic. Pulmonx Corp. has the first minimally invasive valve to treat severe emphysema, which is a form of COPD that accounts for about one-quarter of the patients.
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Phase III data for HL-301 in acute bronchitis

May 5, 2020

Mesoblast initiates phase II/III study of remestemcel-L in patients with COVID-19 ARDS

May 4, 2020
1QBit-xrAI-Chest-X-ray-Abnormal.png

Health Canada accelerates approval of AI-driven COVID-19 tool

April 30, 2020
By David Godkin
TORONTO – Within a week of completing clinical trials the chest radiography AI tool developed by Vancouver, B.C.-based 1Qbit Inc. has been given the all-clear from Health Canada for deployment across the country. The XrAI was originally developed to better identify patients with respiratory illness including SARS, pneumonia and tuberculosis (TB), but then in February was tested on a publicly available data set of COVID-19 X-ray images.
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