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Extremely Robust Acute Respiratory Distress Syndrome Pipeline Featuring 100+ Companies Expected to Change the Pace of the ARDS Treatment | DelveInsight

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The acute respiratory distress syndrome (ARDS) pipeline is experiencing substantial growth, with over 100 active players working on 105 pipeline therapies. The increase in ARDS incidence is driving research and development in this sector, making it a lucrative market for new treatments. Companies like Biocon, NRx Pharmaceuticals, and Veru Healthcare are at the forefront of this effort, focusing on innovative therapies such as Itolizumab and Lenzilumab. Notably, Tetra Bio-Pharma secured $150,000 in funding for its ARDS-003 oral formulation development. The report highlights diverse therapeutic approaches, including cell replacements and targeted pharmacological agents.

Positive
  • Over 100 active companies developing 105+ therapies for ARDS.
  • Increased funding for ARDS treatment projects, exemplified by Tetra Bio-Pharma's $150,000 funding.
  • Focus on innovative therapies such as Itolizumab and Lenzilumab from leading firms.
Negative
  • None.

The rise in the incidence of ARDS stimulates the research and development of the drug, as it is likely to provide an appropriate environment for newer products to be profitable. Companies across the globe have shifted their focus toward the treatment of ARDS. The increase in the incidence will potentiate the treatment market for ARDS. Treatment goals, such as "permissive atelectasis", "permissive hypercapnia", and even "permissive hypoxemia", have been introduced as targets of ventilatory support. Together with the increased knowledge and understanding of how mechanical ventilation can harm the lungs, a major effort has been put into preventing or shortening the use of mechanical ventilation as much as possible and using settings that are considered to be "lung-protective." Several other supportive care options are available, but they all do not withstand the current needs of patients for this indication.

LAS VEGAS, March 30, 2023 /PRNewswire/ -- DelveInsight's 'Acute Respiratory Distress Syndrome Pipeline Insight – 2023' report provides comprehensive global coverage of available, marketed, and pipeline acute respiratory distress syndrome therapies in various stages of clinical development, major pharmaceutical companies are working to advance the pipeline space and future growth potential of the acute respiratory distress syndrome pipeline domain.

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Key Takeaways from the Acute Respiratory Distress Syndrome Pipeline Report

  • DelveInsight's acute respiratory distress syndrome pipeline report depicts a robust space with 100+ active players working to develop 105+ pipeline therapies for acute respiratory distress syndrome treatment. 
  • Key acute respiratory distress syndrome companies such as Biocon, NRx Pharmaceuticals, Humanigen, Mesoblast, Sage Therapeutics, Evgen Pharma, Dimerix Bioscience, Vanda Pharmaceuticals, EUSA Pharma, Veru Healthcare, Foresee Pharmaceuticals, BioMarck Pharmaceuticals, Boehringer Ingelheim, Biohaven Pharmaceuticals, Biophytis, NovImmune SA, Constant Therapeutics, Windtree Therapeutics, Acticor Biotech, Direct Biologics, F4 Pharma, Apeiron Biologics, Trevena, Synact Pharma, Pluristem Therapeutics, UCB Pharma, Chiesi Farmaceutici, and others are evaluating new acute respiratory distress syndrome drugs to improve the treatment landscape.
  • Promising acute respiratory distress syndrome pipeline therapies in various stages of development include Itolizumab, ZYESAMI, Lenzilumab, Remestemcel-L, Brexanolone, SFX-01, DMX-200, Tradipitant, Siltuximab, VERU 111, BIO 11006, FP025, Alteplase, Sarconeos Zavegepant, EB 05, USB 002, Sinapultide, Glenzocimab, DB 001, FX06, APN01, TRV 027, AP1189, PLX PAD, Zilucoplan, CHF5633, and others.
  • In March 2023, Tetra Bio-Pharma received up to $150,000 in funding from the National Research Council of Canada Industrial Research Assistance Program (NRC IRAP) to support a research and development project to enable the development of its ARDS-003 oral formulation. Specifically, the funds will be used to optimize the formulation and perform animal non-GLP Pharmacokinetic Studies.
  • In February 2021, Avid Bioservices and Humanigen announced that they had entered into a manufacturing services agreement to expand production capacity for lenzilumab. Under the terms of this Current Good Manufacturing Practice (cGMP) agreement, Avid would initiate technical transfer and analytical validation activities for lenzilumab with the goal of delivering cGMP drug substance batches to support Humanigen's regulatory and potential commercial activities.

Request a sample and discover the recent advances in ARDS drug treatment @ Acute Respiratory Distress Syndrome Pipeline Report

The acute respiratory distress syndrome pipeline report provides detailed profiles of pipeline assets, a comparative analysis of clinical and non-clinical stage acute respiratory distress syndrome drugs, inactive and dormant assets, a comprehensive assessment of driving and restraining factors, and an assessment of opportunities and risks in the acute respiratory distress syndrome clinical trial landscape.

Acute Respiratory Distress Syndrome Overview

Acute respiratory distress syndrome (ARDS) is a rapidly progressing condition that primarily affects the critically ill. The most serious complication of ARDS is fluid leaking into the lungs, making breathing difficult or impossible. The ARDS causes are classified as direct or indirect lung injuries. Direct lung injuries include pneumonia, aspiration, trauma, and others. Examples of indirect lung injuries include pancreatic inflammation, severe infection (also known as sepsis), blood transfusions, burns, and pharmaceutical responses.

ARDS symptoms include shortness of breath, coughing, and fever; in some cases, high heart rates and rapid breathing have also been observed. Patients with ARDS may experience chest pain, especially during inhalation, and some may develop blue nails and lips due to drastically reduced oxygen levels in the blood. Mechanical ventilation, stress ulcer and venous thromboembolism prevention, nutritional support, and underlying damage therapy are all part of the acute respiratory distress syndrome treatment.

Find out more about drugs for ARDS @ New Acute Respiratory Distress Syndrome Drugs 

A snapshot of the Acute Respiratory Distress Syndrome Pipeline Drugs mentioned in the report:

Drugs

Company

Phase 

MoA

RoA

Remestemcel-L 

Mesoblast

Phase III

Cell replacements

Intravenous

SFX-01

Evgen Pharma

Phase II/III

Androgen receptor antagonists; Hedgehog protein modulators; Histone deacetylase inhibitors; NF E2 related factor 2 stimulants; Wnt signalling pathway modulators

Oral

EB05

Edesa Biotech/Light Chain Bio

Phase II/III

Toll-like receptor 4 antagonists

Intravenous

MultiStem

Athersys/Healios

Phase II/III

Cell replacements

Intravenous

Alteplase

Boehringer Ingelheim/Genentech

Phase II/III

Fibrinolytic agents; Plasminogen activator stimulants; Plasminogen activators

Intravenous

BIO-11006 

BioMarck Pharmaceuticals

Phase II

Myristoylated alanine-rich C kinase substrate inhibitors

Inhalation

Lucinactant

Windtree Therapeutics

Phase II

Cell membrane permeability enhancers

Intratracheal

Solnatide

Apeptico Forschung und Entwicklung GmbH

Phase II

Sodium channel agonists

Inhalation

 

Learn more about the emerging acute respiratory distress syndrome pipeline therapies @ ARDS Clinical Trials

Acute Respiratory Distress Syndrome Therapeutics Assessment

The acute respiratory distress syndrome pipeline report proffers an integral view of acute respiratory distress syndrome emerging novel therapies segmented by stage, product type, molecule type, mechanism of action, and route of administration.

Scope of the Acute Respiratory Distress Syndrome Pipeline Report 

  • Coverage: Global 
  • Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination
  • Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III
  • Therapeutics Assessment By Route of Administration: Oral, Parenteral, Intravenous, Subcutaneous, Topical
  • Therapeutics Assessment By Molecule Type: Monoclonal Antibody, Peptides, Polymer, Small molecule, Gene therapy
  • Therapeutics Assessment By Mechanism of Action: Androgen receptor antagonists, Hedgehog protein modulators, Histone deacetylase inhibitors, NF E2 related factor 2 stimulants, Wnt signalling pathway modulators, Cell replacements, Toll-like receptor 4 antagonists, Fibrinolytic agents, Plasminogen activator stimulants, Plasminogen activators, Myristoylated alanine-rich C kinase substrate inhibitors, Cell membrane permeability enhancers, Sodium channel agonists
  • Key Acute Respiratory Distress Syndrome Companies: Biocon, NRx Pharmaceuticals, Humanigen, Mesoblast, Sage Therapeutics, Evgen Pharma, Dimerix Bioscience, Vanda Pharmaceuticals, EUSA Pharma, Veru Healthcare, Foresee Pharmaceuticals, BioMarck Pharmaceuticals, Boehringer Ingelheim, Biohaven Pharmaceuticals, Biophytis, NovImmune SA, Constant Therapeutics, Windtree Therapeutics, Acticor Biotech, Direct Biologics, F4 Pharma, Apeiron Biologics, Trevena, Synact Pharma, Pluristem Therapeutics, UCB Pharma, Chiesi Farmaceutici, and others.
  • Key Acute Respiratory Distress Syndrome Pipeline Therapies:  Itolizumab, ZYESAMI, Lenzilumab, Remestemcel-L, Brexanolone, SFX-01, DMX-200, Tradipitant, Siltuximab, VERU 111, BIO 11006, FP025, Alteplase, Sarconeos Zavegepant, EB 05, USB 002, Sinapultide, Glenzocimab, DB 001, FX06, APN01, TRV 027, AP1189, PLX PAD, Zilucoplan, CHF5633, and others.

Dive deep into rich insights for new drugs for ARDS treatment; visit @ Acute Respiratory Distress Syndrome Medications

Table of Contents

1.

Acute Respiratory Distress Syndrome Pipeline Report Introduction

2.

Acute Respiratory Distress Syndrome Pipeline Report Executive Summary

3.

Acute Respiratory Distress Syndrome Pipeline: Overview

4.

Analytical Perspective In-depth Commercial Assessment

5.

Acute Respiratory Distress Syndrome Clinical Trial Therapeutics

6.

Acute Respiratory Distress Syndrome Pipeline: Late Stage Products (Pre-registration)

7.

Acute Respiratory Distress Syndrome Pipeline: Late Stage Products (Phase III)

8.

Acute Respiratory Distress Syndrome Pipeline: Mid Stage Products (Phase II)

9.

Acute Respiratory Distress Syndrome Pipeline: Early Stage Products (Phase I)

10.

Acute Respiratory Distress Syndrome Pipeline Therapeutics Assessment

11.

Inactive Products in the Acute Respiratory Distress Syndrome Pipeline

12.

Company-University Collaborations (Licensing/Partnering) Analysis

13.

Key Companies

14.

Key Products in the Acute Respiratory Distress Syndrome Pipeline

15.

Unmet Needs

16.

Market Drivers and Barriers

17.

Future Perspectives and Conclusion

18.

Analyst Views

19.

Appendix

 

For further information on the acute respiratory distress syndrome pipeline therapeutics, reach out @ Acute Respiratory Distress Syndrome Drug Treatment

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FAQ

What is the current status of the ARDS drug pipeline as of March 2023?

The ARDS drug pipeline includes over 100 active companies developing more than 105 therapies, indicating a dynamic growth phase.

Which companies are leading the ARDS treatment market?

Key players in the ARDS treatment market include Biocon, NRx Pharmaceuticals, Veru Healthcare, and Humanigen.

What is the significance of the $150,000 funding for Tetra Bio-Pharma?

The funding supports the development of Tetra Bio-Pharma's ARDS-003 oral formulation, highlighting ongoing investment in ARDS treatment.

What kinds of therapies are being developed for ARDS?

Therapies under development range from cell replacement treatments to various targeted pharmacological agents.

What are the goals for ARDS treatment according to recent reports?

Recent reports highlight treatment goals like permissive atelectasis and hypercapnia, along with efforts to minimize mechanical ventilation.

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