Acute Respiratory Distress Syndrome Pipeline Drugs and Companies Report: Analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments
DelveInsight Business Research LLP
8 min read
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.
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).
Acute Respiratory Distress Syndrome (ARDS) is a life-threatening condition of seriously ill patients, characterized by poor oxygenation, pulmonary infiltrates, and acuity of onset.
VERU-111 (Sabizabulin) is a cytoskeleton disruptor, has both anti-viral and anti-inflammatory activity and could be effective against the SARS-CoV-2 virus by disrupting its intracellular transport along the microtubules. It is currently being evaluated in the Phase III stage of development.
Tradipitant: Vanda Pharmaceuticals
Tradipitant (VLY-686), a small molecule neurokinin-1 receptor (NK-1R) antagonist. The drug is currently being evaluated in Phase III clinical studies in patients with atopic dermatitis, COVID 2019 infections, gastroparesis, and Phase II clinical studies to treat motion sickness and pruritus.
FP-025: Foresee Pharmaceuticals
FP-025 is an oral non-competitive small molecule inhibitor of Matrix Metalloproteinase-12/Macrophage elastase (MMP-12). This enzyme acts as a key mediator of matrix degradation and remodeling in normal development and maintenance. The drug is currently being evaluated in Phase II/III clinical study to treat patients with severe to critical COVID 19 with associated ARDS and in Phase II clinical study to treat asthma and COPD.
HLCM051(MultiStem): Athersys
MultiStem cell therapy is a patented and proprietary allogeneic “off-the-shelf” stem cell product. The cells are developed from a particular class of stem cells called Multipotent Adult Progenitor Cells, or MAPC, and are distinct from mesenchymal stem cells (MSCs) and other cell types. MultiStem cell therapy is currently being evaluated in Phase III clinical trials to treat patients with ischemic stroke, Phase II/III clinical study for thARDSeatment, and Phase I/II clinical study to treat severe trauma. In addition, the Company’s partner in Japan, Healios, is also evaluating the therapy in its ischemic stroke study (TREASURE) and has recently completed enrollment in its ARDS (ONE-BRIDGE) study using MultiStem cell therapy.
What are the current options for Acute Respiratory Distress Syndrome treatment?
How many companies are developing therapies to treat Acute Respiratory Distress Syndrome?
How many ARDS emerging therapies in the early-stage, mid-stage, and late development stages to treat Acute Respiratory Distress Syndrome?
What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, and significant licensing activities that will impact the Acute Respiratory Distress Syndrome market?
Which are the dormant and discontinued products and the reasons for the same?
What is the unmet need for current therapies to treat Acute Respiratory Distress Syndrome?
What are the current novel therapies, targets, mechanisms of action, and technologies developed to overcome the limitation of existing ARDS therapies?
What critical designations have been granted for the emerging therapies for Acute Respiratory Distress Syndrome?
How many patents are granted and pending for the emerging therapies to treat Acute Respiratory Distress Syndrome?
Key companies working in the Acute Respiratory Distress Syndrome market are Faron Pharmaceuticals, PhaseBio Pharmaceuticals, Sage Therapeutics, Chimerix, Direct Biologics, Kiniksa Pharmaceuticals, and others.
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