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BioWorld - Sunday, June 14, 2026
Home » Topics » Disease categories and therapies » Respiratory

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3D lung segmentation

Medi-Scan’s digital tool converts ultrasound images to 3D at the point of care

March 9, 2021
By Meg Bryant
Medi-Scan Inc. has emerged from stealth mode with cloud-based software that converts the data on ultrasound analog 2D grayscale images into a digital 3D high-definition (HD) format in less than two minutes. The company is currently focusing its efforts on the heart and lungs, with the aim of providing quick, point-of-service evaluation and triaging of patients with heart disease and other conditions, including COVID-19.
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REGN1908-1909 ameliorates bronchoconstriction in patients with cat-allergy asthma

March 8, 2021

FDA approves Actemra for rare scleroderma-linked lung disease

March 5, 2021
By Michael Fitzhugh
More than a decade after first approving Actemra (tocilizumab) for the treatment of rheumatoid arthritis, the FDA has added a sixth use to its label: slowing the rate of decline in pulmonary function in adult patients with systemic sclerosis-associated interstitial lung disease.
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FDA approves Actemra for systemic sclerosis-associated interstitial lung disease

March 5, 2021

Cough triggers and symptoms among patients treated in COUGH-1 and COUGH-2

March 5, 2021

Nuformix reports preclinical data on NXP-002 in combination therapy for IPF

March 4, 2021

Benralizumab achieves OCS elimination or reduction in OCS-dependent asthmatics

March 4, 2021

Promising results from phase III NAVIGATOR study of tezepelumab

March 3, 2021
Software screenshot

Fifth Eye launches ML-based tool to predict hemodynamic instability

March 2, 2021
By Meg Bryant
The FDA has granted de novo authorization to Fifth Eye Inc. for its Analytic for Hemodynamic Instability (AHI), a machine learning (ML)-based, real-time indicator of patient deterioration. Commercialization of the software device, which continuously monitors patients with an electrocardiogram (ECG) for signs of deterioration, got underway on March 1.
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FDA agrees to advance VERU-111 into phase III study in COVID-19 patients at high risk for ARDS

March 2, 2021
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