DelveInsight’s, “Respiratory Syncytial Virus Pipeline Insight, 2023,” report provides comprehensive insights about 50+ companies and 50+ pipeline drugs in Respiratory Syncytial Virus pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
In the Respiratory Syncytial Virus pipeline report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, Respiratory Syncytial Virus NDA approvals (if any), and product development activities comprising the technology, Respiratory Syncytial Virus (RSV) collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Key takeaways from the Respiratory Syncytial Virus Pipeline Report
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Respiratory Syncytial Virus Overview
Respiratory syncytial virus (RSV) is a very common cause of respiratory tract infection, particularly in children. Nearly all children have been infected by age 4 years, many in the first year of life. Infection does not provide complete immunity, so reinfection is common, although usually less serious. Outbreaks typically occur in winter and early spring.
Recent Developments Activities in the Respiratory Syncytial Virus Treatment Landscape
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Respiratory Syncytial Virus Emerging Drugs
This candidate vaccine contains a recombinant subunit pre-fusion RSV antigen (RSVPreF3) combined with GSK’s proprietary AS01 adjuvant, which is also used in GSK’s shingles vaccine. Currently, it is in phase III of development stage for the treatment of Respiratory Syncytial Virus (RSV).
MEDI8897 is a monoclonal antibody (mAb) for the prevention of lower respiratory tract illness (LRTI) caused by respiratory syncytial virus (RSV), the most prevalent cause of LRTI among infants and young children. Currently, it is in phase III of development stage.
Sisunatovir is an orally administered fusion inhibitor designed to block RSV replication by inhibiting RSV F-mediated fusion of RSV with the host cell. Preclinical tests showed sisunatovir to have an excellent toxicity profile with an attractive therapeutic index. In Phase 1 clinical studies, sisunatovir showed excellent exposure with no serious adverse events being reported. In 2018, results from a Phase 2a challenge study in healthy adult volunteers were reported in which sisunatovir produced statistically significant reductions in viral load and clinical symptoms. ReViral has initiated two international multicentre Phase 2 clinical studies of sisunatovir in pediatric and adult high-risk patient populations.
Respiratory Syncytial Virus Pipeline Therapeutics Assessment
There are approx. 50+ key companies which are developing the therapies for Respiratory Syncytial Virus (RSV). The companies which have their Respiratory Syncytial Virus (RSV) drug candidates in the most advanced stage, i.e. phase III include, GlaxoSmithKline.
For further information, refer to the detailed Respiratory Syncytial Virus Unmet Needs, Respiratory Syncytial Virus Market Drivers, and Market Barriers, click here for Respiratory Syncytial Virus Ongoing Clinical Trial Analysis
Scope of the Respiratory Syncytial Virus Pipeline Report
Dive deep into rich insights for drugs for Respiratory Syncytial Virus Market Drivers and Respiratory Syncytial Virus Market Barriers, click here @ Respiratory Syncytial Virus Unmet Needs and Analyst Views
Table of Content
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