The global sterile antimicrobial gel market is projected to grow from approximately US$ 1.44 billion in 2023 to US$ 3.05 billion by 2034, with a CAGR of 7.05% from 2024 to 2034. This growth is driven by the rising demand for the gel’s use in preventing infections in chronic wounds, traumatic injuries, and post-operative care, owing to its biocompatibility and wound healing properties.
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In September 2024, the U.S. Department of Health and Human Services (HHS) announced funding for a project called “Transforming Antibiotic R&D with Generative AI to Stop Emerging Threats (TARGET)” through the Advanced Research Projects Agency for Health.
The G7 Finance and Health Ministers committed to implementing existing antimicrobial resistance (AMR) strategies, addressing the market failures of antibiotics, and fostering economic conditions to preserve the effectiveness of essential antibiotics.
In November 2023, the Food and Drug Administration (FDA) proposed new requirements for a premarket approval application (PMA) for certain wound dressings formulated as creams, gels, or ointments, as well as solid wound dressings and liquid wound washes containing medically important antimicrobials. These products must comply with the PMA requirements of the Federal Food, Drug, and Cosmetic Act (FD&C Act). Solid wound dressings and other antimicrobial-infused products are designed to maintain appropriate moisture levels and provide protection for wounds.
Medically essential antimicrobials are included in these dressings to minimize microbial growth and create an antimicrobial barrier against infections. Patients are the primary end users of these formulations and liquid wound washes, which are water-based solutions used to clean external wounds. The FDA assesses the benefits and risks of these antimicrobial products, considering potential adverse tissue reactions, immunological responses, pathogen transmission, delayed wound healing, and infection risks.
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