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Pulmonary Patient Articles & Analysis

24 news found

AngioDynamics Completes Patient Enrollment in APEX-AV Study Assessing AlphaVac F1885 System in Treatment of Pulmonary Embolism

AngioDynamics Completes Patient Enrollment in APEX-AV Study Assessing AlphaVac F1885 System in Treatment of Pulmonary Embolism

(NASDAQ: ANGO), a leading and transformative medical technology company focused on restoring healthy blood flow in the body’s vascular system, expanding cancer treatment options and improving patient quality of life, today announced the completion of patient enrollment in the Acute Pulmonary Embolism Extraction Trial with the AlphaVac ...

ByAngioDynamics, Inc.


Third Pole Therapeutics Receives $32M Strategic Equity Investment to Accelerate its Tankless Inhaled Nitric Oxide (iNO) Platform

Third Pole Therapeutics Receives $32M Strategic Equity Investment to Accelerate its Tankless Inhaled Nitric Oxide (iNO) Platform

” “I am also pleased to report that eNOfit™, our novel miniaturized mobile-wearable nitric oxide device designed to provide ’on-the-go’ treatment for patients suffering from severe COPD and ILD (pulmonary fibrosis), is scheduled to enter clinical trials in the next few months. ...

ByThird Pole Therapeutics, Inc.


Inari Medical Announces Results from the Fully Enrolled 800-patient US Cohort of the FlowTriever FLASH Registry

Inari Medical Announces Results from the Fully Enrolled 800-patient US Cohort of the FlowTriever FLASH Registry

(NASDAQ: NARI) (“Inari”) a medical device company focused on developing products to treat and transform the lives of patients suffering from venous and other diseases, announced positive outcomes of the fully enrolled 800-patient FLASH registry in pulmonary embolism (“PE”). ...

ByInari Medical


Inversago Pharma presents data on INV-101 in Idiopathic Pulmonary Fibrosis at the ERS Congress 2022

Inversago Pharma presents data on INV-101 in Idiopathic Pulmonary Fibrosis at the ERS Congress 2022

Glenn Crater, CMO at Inversago pointed out: “These encouraging results obtained using a well-accepted preclinical model for lung fibrosis show that zevaquenabant hold promise as a novel treatment option for pulmonary fibrosis. With only two treatments for IPF available, the potential of zevaquenabant in this indication as an add-on therapy is important for ...

ByInversago Pharma


Cordis-X Makes Strategic Investment in Adient Medical, Developer of First Fully Absorbable Inferior Vena Cava (IVC) Filter

Cordis-X Makes Strategic Investment in Adient Medical, Developer of First Fully Absorbable Inferior Vena Cava (IVC) Filter

"The Adient fully absorbable filter solution creates a new paradigm to protect patients from pulmonary embolus," Dr. Durack shared. "I am thrilled to be part of the collaborative team of Adient, Cordis, and Cordis-X and to see this groundbreaking approach come to fruition." ...

ByAdient Medical, Inc.


Saluda Medical Appoints Doug Godshall as Chairman of the Board

Saluda Medical Appoints Doug Godshall as Chairman of the Board

He is also a member of the Board of Directors of the Medical Device Manufacturers Association and Chairman of the Board of Gala Therapeutics, a privately held medical device company that is dedicated to developing disease-modifying therapies for patients with pulmonary diseases. Previously, Mr. Godshall was President, Chief Executive Officer and Director of ...

BySaluda Medical Pty Ltd.


Lupin Receives Approval from U.S. FDA for Arformoterol Tartrate Inhalation Solution15 mcg (base)/2 ml

Lupin Receives Approval from U.S. FDA for Arformoterol Tartrate Inhalation Solution15 mcg (base)/2 ml

Arformoterol Tartrate Inhalation Solution 15 mcg (base)/2 ml, Unit-dose Vials are indicated for the long-term maintenance treatment of bronchoconstriction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema.Arformoterol Tartrate Inhalation Solution is for use by nebulization only. ...

ByLupin Limited


Third Pole Therapeutics Closes $25M Financing - eNOfit Wearable Device Now Ready for Clinical Trials

Third Pole Therapeutics Closes $25M Financing - eNOfit Wearable Device Now Ready for Clinical Trials

Athenson continued, “We are now much closer to improving the lives of 1.2M patients battling severe COPD and ILD (pulmonary fibrosis) and who struggle with each breath to perform the day-to-day activities that most people take for granted. ...

ByThird Pole Therapeutics, Inc.


Galaxy Medical Enrolls First Patients in SPACE-AF Study SAN

Galaxy Medical Enrolls First Patients in SPACE-AF Study SAN

Patients with persistent atrial fibrillation often require electrical isolation beyond simple pulmonary vein isolation and for years we have been seeking a safe, predictable, and effective energy source to do so. ...

ByGalvanize Therapeutics, Inc.


Berlin Heart Received CE Mark and Announces First Implantation of the Latest Cannula Generation to Treat Heart Patients Waiting for a Donor Heart

Berlin Heart Received CE Mark and Announces First Implantation of the Latest Cannula Generation to Treat Heart Patients Waiting for a Donor Heart

Improvements in the field of mechanical circulatory support and the further development of ventricular assist devices enable critically ill heart patients to recover and bridge the often very long waiting periods for a donor heart. Berlin Heart has developed a cannula that intends to a more convenient surgical handling during implantation and an adaptation to the individual needs ...

ByBerlin Heart GmbH


Galaxy Medical Releases ECLIPSE-AF Remapping Data at Stanford Biodesign Retreat and Update on System Interoperability

Galaxy Medical Releases ECLIPSE-AF Remapping Data at Stanford Biodesign Retreat and Update on System Interoperability

SAN CARLOS, California, July 28, 2021 — Galaxy Medical announced today that the ECLIPSE-AF 90-day remapping data, presented at the Stanford BioDesign New Arrhythmia Technologies retreat, demonstrated durable lesions and chronic pulmonary vein isolation (PVI). Also, the company has recently treated patients in the same study using CE-Marked catheters and ...

ByGalvanize Therapeutics, Inc.


Xeltis initiates first-ever pivotal trial of a synthetic restorative pulmonary heart valve

Xeltis initiates first-ever pivotal trial of a synthetic restorative pulmonary heart valve

Following implantation, Xeltis’ synthetic restorative pulmonary heart valves evolve into fully functioning, natural heart valves through colonization by the patient’s own tissue. ...

ByXELTIS BV


Towards a cure for Mycobacterium abscessus disease using inhaled tigecycline

Towards a cure for Mycobacterium abscessus disease using inhaled tigecycline

Following successful research into a potential treatment option, PureIMS, Radboudumc and Sever Pharma Solutions (until recently known as Disphar International) are now teaming up to develop an effective cure for this chronic and debilitating disease. Worldwide, over 30,000 patients suffer from Mycobacterium abscessus disease. This number has been steadily rising in recent years, ...

ByPureims B.V.


MediPines AGM100 Voted as Finalist in Medical Design Excellence Awards, MDEA 2021

MediPines AGM100 Voted as Finalist in Medical Design Excellence Awards, MDEA 2021

“The ultimate goal in designing and engineering this respiratory solution was to improve clinical workflow efficiency and patient outcomes. We are essentially bringing the pulmonary lab right to the patient’s ...

ByMediPines


Berlin Heart Today Announces CE Approval and First Implantation of an Innovative Bridging Solution for Single Ventricle Patients

Berlin Heart Today Announces CE Approval and First Implantation of an Innovative Bridging Solution for Single Ventricle Patients

This innovative therapy was developed to improve the end-organ function and hemodynamics of these patients with univentricular physiology through the support of the sub-pulmonary circulation. ...

ByBerlin Heart GmbH


Aidoc launches the first ai-based automated notification solution for high-risk pulmonary embolism patients

Aidoc launches the first ai-based automated notification solution for high-risk pulmonary embolism patients

Aidoc, the leading provider of enterprise AI solutions, announced today the launch of an industry first: an AI-based automated activation solution that facilitates rapid risk assessment and care coordination for high-risk pulmonary embolism (PE) patients. Aidoc’s PE Care Coordination includes Aidoc’s FDA-cleared solution for triage and notification ...

ByAidoc


AIDOC and IMBIO partner to provide an industry first ai solution to prioritize suspected pulmonary embolism and automatically calculate RV/LV  ratio

AIDOC and IMBIO partner to provide an industry first ai solution to prioritize suspected pulmonary embolism and automatically calculate RV/LV ratio

The partnership is intended to provide thoracic radiologists and pulmonary embolism management programs timely notification of pulmonary embolism cases combined with automated RV/LV ratio calculations to potentially improve patient severity assessment and expedite treatment. ...

ByAidoc


Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Applying non-invasive electrical stimulation to the expiratory abdominal muscles may reduce abdominal muscle atrophy and markedly reduce the number of days adult patients require mechanical ventilation – a potentially important finding for weaning ventilated patients, including seriously ill COVID-19 patients, and improving patient outcomes. Liberate Medical today announced the results of ...

ByLiberate Medical, LLC


Dexamethasone reportedly part of President Trump’s Treatment

Dexamethasone reportedly part of President Trump’s Treatment

AVM has FDA permission to begin clinical trials using AVM0703 to treat patients with COVID-19- and influenza-mediated Acute Respiratory Distress Syndrome (ARDS). ...

ByAVM Biotechnology


VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

Current methods of respiratory muscle training cannot be used when patients are sedated or delirious, which is common among critically ill patients. ...

ByLiberate Medical, LLC

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