DelveInsight’s, “Candidemia Pipeline Insight 2023,” report provides comprehensive insights about 4+ companies and 4+ pipeline drugs in Candidemia 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.
For Candidemia Emerging drugs, the Candidemia pipeline analysis report provides a 360° view of the therapeutics landscape by development point, product type, route of administration, molecule type, and MOA. The Candidemia pipeline research covers business opportunities, challenges, future partnerships, strong competitors, and growth strategies.
In the Candidemia Pipeline Report, a detailed description of the drug is given which includes the mechanism of action of the drug, Candidemia clinical trials studies, Candidemia NDA approvals (if any), and product development activities comprising the technology, Candidemia collaborations, licensing, mergers and acquisition, funding, designations, and other product-related details.
Key takeaways from the Candidemia Pipeline Report
To explore more information on the latest breakthroughs in the Candidemia Pipeline treatment landscape of the report, click here @ Candidemia Pipeline Outlook
Candidemia Overview
Candidemia is defined as the presence of Candida species in the blood. It is the most common fungal bloodstream infection in hospitalized patients. Candida albicans is the most common cause of candidemia, representing 35% to 60% of isolates. Candida parapsilosis, Candida tropicalis, Candida glabrata and Candida krusei, are the most common nonalbicans Candida species identified in cultures. Most common risk factors include critical illness and prolonged intensive care unit stay.
Candidemia Emerging Drugs Profile
Cidara is developing a novel once-weekly echinocandin, rezafungin, for both the treatment and prevention of serious fungal infections, such as candidemia and invasive candidiasis. The structure and properties of rezafungin are specifically designed to improve upon a clinically validated mechanism, enhancing its efficacy and safety potential for patients. For the treatment of candidemia and invasive candidiasis, rezafungin has designations for Qualified Infectious Disease Product, or QIDP, Fast Track, and Orphan Drug. QIDP and Orphan Drug designations together provide a total of 12 years of marketing exclusivity in the United States from the time of FDA approval. Originally, this compound was owned by Seachaid Pharmaceuticals. Rezafungin acetate is now licensed by Mundipharma International and under the development of Cidara Therapeutics. The drug is currently being evaluated in Phase III stage of development for the treatment of patients with Candidemia.
For further information, refer to the detailed Candidemia Unmet Needs, Candidemia Market Drivers, and Candidemia Market Barriers, click here for Candidemia Ongoing Clinical Trial Analysis
Candidemia Pipeline Therapeutics Assessment
There are approx. 4+ key companies which are developing the therapies for Candidemia. The companies which have their Candidemia drug candidates in the most advanced stage, i.e. Phase III include, Cidara Therapeutics.
Candidemia Pipeline: Phases
Request a sample and discover the recent advances in Candidemia Ongoing Clinical Trial Analysis and Medications, click here @ Candidemia Treatment Landscape
Scope of the Candidemia Pipeline Report
Dive deep into rich insights for drugs for Candidemia Market Drivers and Candidemia Market Barriers, click here @ Candidemia Unmet Needs and Analyst Views
Table of Content
Got Queries? Find out the related information on Candidemia Mergers and acquisitions, Candidemia Licensing Activities @ Candidemia Emerging Drugs, and Recent Trends
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