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Ireland-based Fountain Healthcare Partners has raised another €125 million ($131 million) for its third lifesciences fund – 25% ahead of its target – and says it will pump most of the money into European therapeutics and medical device companies. The third fund is now closed.
Additionally, a collaboration with NurExone is creating an intranasal delivery system for exosome-based therapies targeting spinal cord injuries, with potential expansion into other neurological uses. Polyrizon’s focus on intranasal protection aligns with a rapidly expanding market in drugdelivery innovation.
Ayesha also talked about the FDAapproval of AstraZeneca’s asthma inhaler Airsupra, the first-in-class drug that contains both a beta agonist and corticosteroid. The inhaler is approved as a rescue medication for adults with asthma to help treat bronchoconstriction and asthma attacks.
Related: Genentech’s New Ocular Implant DrugDelivery System for Macular Degeneration Could Be a Game Changer. The FDAapproval of Vuity exemplifies our continued pursuit of innovative new treatments that push the boundaries of what’s possible in eye care.”. Vuity is available by prescription.
These issues primarily stem from patients and healthcare providers miscalculating or incorrectly administering the drug. Compounded semaglutide products, unlike the US Food and Drug Administration (FDA)-approved ones, can vary widely in strength and packaging, making it easy for mistakes to happen.
The rankings are based on each companys ability to tackle critical challenges from drugdelivery and diagnostics to personalized therapies using cutting-edge science. With a 30-month shelf life and rapid absorption, Neffy offers an on-the-go alternative to auto-injectors. Here are 20 companies leading the way in 2025.
The team also learned about the FDAapproval of Genentech’s new ocular implant drugdelivery system, called Susvimo, for the treatment of neovascular, or wet, age-related macular degeneration (nAMD). Read the full articles here: FDA Authorizes Pfizer/BioNTech COVID-19 Vaccine for Kids 5 to 11.
Valneva SE, who developed the worlds first FDA-approved chikungunya vaccine , has now unveiled promising Phase III data for its single-shot chikungunya vaccine, IXCHIQ, in adolescents aged 12 to 17. Following the announcement, Valnevas stock rose by 1.4%.
Ocrevus Zunovo uses Halozyme Therapeutics’ Enhanze drugdelivery technology , which enhances absorption by temporarily increasing the permeability of the subcutaneous tissue. The enzyme rHuPH20 enables rapid dispersion of the drug into the bloodstream.
XTALKS : Changes are Coming to Prefilled Injectable DrugDelivery Systems Live and On-Demand: Thursday, September 12, 2024, at 1pm EDT (10 am PDT) Register for this webinar today to learn more about the future of injectable drugdelivery systems and the impact of blow-fill-seal technology.
XTALKS WEBINAR: DrugDelivery — Evaluating Off-The-Shelf and Novel DrugDelivery Solutions Live and On-Demand: Tuesday, July 11, 2023, at 1pm EDT (10am PDT) Register for this free webinar to learn about important tradeoffs when considering an off-the-shelf (OTS) drugdelivery platform vs. novel development.
Airsupra is being jointly developed by AstraZeneca and Avillion, also a UK-based drug development company that received funding from. Related: Lung Disease Diagnostic Xenoview Gets FDAApproval for Use with MRI. The FDAapproval was based on results from the MANDALA, DENALI and TYREE Phase III studies.
One of the biggest challenges with developing therapies to treat CNS disorders is the delivery of systemically administered investigational products (IPs) to the brain, which is limited by the blood-brain barrier. Some methods of direct CNS administration include intrathecal, intraparenchymal and intracerebroventricular (ICV) delivery.
Drug-eluting stents (DES): DES reduce the incidence of restenosis and are coated with drugs that inhibit scar tissue growth. DCBs: DCBs, such as the Agent DCB, combine mechanical widening of the artery with drugdelivery to the vessel wall to prevent cell proliferation.
This innovative formulation uses Halozyme’s Enhanze drugdelivery technology, facilitating the subcutaneous administration of biologics. New CIDP Treatments on the Market In January 2024, the FDAapproved Takeda’s Gammagard Liquid for the treatment of CIDP in adults.
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