MediTelecare Launches Transition to Home Program Via Tele-technology
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Five Things to Know about the Community Health Center Model
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– Commercial launch of Bylvay immediate; available for prescription in the coming days –
– Rare Pediatric Disease Priority Review Voucher issued to Albireo by the FDA –
– Company to host investor conference call on July 21 at 8:30 a.m. ET –
BOSTON, July 20, 2021 (GLOBE NEWSWIRE) Albireo Pharma, Inc. (Nasdaq: ALBO), a rare liver disease company developing novel bile acid modulators, today announced U.S. Food & Drug Administration (FDA) approval of Bylvay (odevixibat), the first drug approved for the treatment of pruritus in all subtypes of progressive familial intrahepatic cholestasis (PFIC). Bylvay is a potent, non-systemic ileal bile acid transport inhibitor (IBATi), which does not require refrigeration and is easily administered as a once-daily capsule or opened and sprinkled onto soft foods. Albireo is launching Bylvay immediately to accelerate availability for the patients and families impacted by PFIC.
The round was led by Rethink Impact with participation from Hearst, Polaris Partners, and Eldridge.
The company intends to use the funds to grow and enhance its smart recommendations engine, advance its predictive support pathways, and launch an online community where families can exchange tips and ideas with other caregivers and gain insights from experts.
Led by Lindsay Jurist-Rosner, Founder and CEO, Wellthy provides a digital care concierge platform that partners with employers to find care for employees and their families. The company uses dedicated Care Coordinators and a technology platform to project manage healthcare for families with complex, chronic, and ongoing care needs.