Acute Respiratory Distress Syndrome Pipeline Drugs and Companies Report: Analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments

There are approximately 120+ key companies that are developing therapies for Acute respiratory distress syndrome. The companies which have their Acute respiratory distress syndrome drug candidates in the mid to advanced stage include Sage Therapeutics, Foresee pharmaceuticals, Veru, Vanda pharmaceutical, and several others.

Los Angeles, USA, Dec. 22, 2021 (GLOBE NEWSWIRE) -- Acute Respiratory Distress Syndrome Pipeline Drugs and Companies Report: Analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments

There are approximately 120+ key companies that are developing therapies for Acute respiratory distress syndrome. The companies which have their Acute respiratory distress syndrome drug candidates in the mid to advanced stage include Sage Therapeutics, Foresee pharmaceuticals, Veru, Vanda pharmaceutical, and several others.

DelveInsight’s “Acute Respiratory Distress Syndrome (ARDS) Pipeline Insight” report provides comprehensive insights about 120+ companies and 120+ pipeline drugs in the Acute Respiratory Distress Syndrome pipeline landscapes. It comprises Acute Respiratory Distress Syndrome pipeline drug profiles, including clinical and non-clinical stage products. It also includes the Acute Respiratory Distress Syndrome therapeutics assessment by product type, stage, route of administration, and molecule type and further highlights the inactive Acute Respiratory Distress Syndrome pipeline products.

Some of the key takeaways from the Acute Respiratory Distress Syndrome Pipeline Report

  • Major companies such as Athersys, Inc, Histocell, BioXcellerator, Altor BioScience, Cartesian Therapeutics, Meridigen Biotech Co., Ltd., Sage Therapeutics, Healios K.K., Chiesi Farmaceutici, Bayer, Altor BioScience, Faron Pharmaceuticals Ltd, AVM Biotechnology LLC, Amyndas Pharmaceuticals S.A., Kinevant Sciences GmbH, Eli Lilly and Company, Suntory Pharmaceutical, Alexion Pharmaceuticals, Laboratoire français de Fractionnement et de Biotechnologies (LFB), Evgen Pharma, Dimerix Bioscience, Mylan, Vanda Pharmaceuticals, Kiniksa Pharmaceuticals Foresee Pharmaceuticals, Boehringer Ingelheim, Staidson (Beijing) Biopharmaceuticals, Biohaven Pharmaceuticals, Chimerix, Edesa Biotech, and others are developing potential drug candidates to improve the Acute Respiratory Distress Syndrome treatment scenario.

  • In February 2021, Athersys announced that it had entered into a cooperation agreement with HEALIOS. The cooperation agreement is intended to reaffirm the mutual commitment to the collaborative development of MultiStem in Japan.

  • In March 2021, Partner Therapeutics announced a licensing and collaboration agreement with SIRS Therapeutics and F4 Pharma to support the development of FX-06. This synthetic peptide has a broad spectrum of potential indications.

  • In June 2020, NeuroRx, in partnership with Relief Therapeutics, announced that the US FDA awarded Fast Track designation to NeuroRx for the investigation of RLF-100 (Aviptadil) for the treatment of acute lung injury/acute respiratory distress syndrome associated with COVID-19.

  • In December 2020, The Food and Drug Administration (FDA) granted Fast Track designation to remestemcel-L for the treatment of acute respiratory distress syndrome (ARDS) due to coronavirus disease 2019 (COVID-19).

  • In November 2020, Novartis announced that it entered into an exclusive worldwide license and collaboration agreement with Mesoblast to develop, commercialize and manufacture remestemcel-L to treat acute respiratory distress syndrome.

  • In September 2020, Dimerix was awarded USD 1 million from the Australian Government's BTB program to support the inclusion of DMX-200 in the REMAP-CAP global study.

  • In September 2020, Athersys announced that MultiStem cell therapy was granted Regenerative Medicine Advanced Therapy (RMAT) designation from the US FDA for the acute respiratory distress syndrome (ARDS) program. In May 2019, US FDA granted Fast Track designation to MultiStem cell therapy for ARDS.

  • In June 2020, Quartesian announced a new partnership with Amyndas Pharmaceuticals for their Phase II clinical study evaluating the efficacy of AMY-101 in COVID-19 patients with acute respiratory distress syndrome (ARDS).