pathogen-killing face masks that were recently approved for use by the U.S. Food and Drug Administration. John Bjornson, Singletto co-founder and CEO (Singletto Photo) “It’s the only FDA ...
A Seattle startup, led by doctors, has just earned FDA approval for a groundbreaking surgical mask that kills viruses on contact. These masks use Oxafence, a technology powered by methylene blue ...
The Nanoleaf LED Light Therapy Face Mask is made of medical-grade materials and has received FDA Class II device certification. (This doesn’t mean the FDA has given Nanoleaf’s ...
Is there anything Airyday can’t do? Their LED face mask emits 3 clinically proven wavelengths (blue, red and near-infrared) to help reduce pigmentation, address ageing and rejuvenate the skin. It also ...
In the interview, he discussed the Dec. 27, 2024, Food and Drug Administration (FDA) approval of subcutaneous Opdivo and Qvantig (nivolumab and hyaluronidase-nvhy) for patients with solid tumors. He ...
A government watchdog examining the FDA’s accelerated approval pathway has released a 32-page report (PDF) that concludes the agency’s controversial endorsement of Biogen’s failed Alzheimer ...
The US Food and Drug Administration (FDA) has approved datopotamab deruxtecan for the treatment of certain patients with unresectable or metastatic hormone receptor (HR)-positive, human epidermal ...
Subcutaneous nivolumab and hyaluronidase-nvhy is FDA-approved for adult solid tumors ... Adverse reactions led to treatment discontinuation in 10% of patients. The recommended dosing for ...
As supported by data from the phase 3 TROPION-Breast01 trial, datopotamab deruxtecan is now an FDA-approved treatment for patients with HR-positive, HER2-negative breast cancer. The FDA has approved ...
Axatilimab has gained FDA approval in 9 mg and 22 mg vials, expanding treatment options for patients with chronic GVHD after 2 prior therapy failures. The FDA has granted approval to axatilimab-csfr ...
The first medication for obstructive sleep apnea has been approved by the US Food and Drug Administration (FDA). On Dec. 20, the FDA announced that the agency has approved Eli Lilly’s Zepbound ...
It's the first time federal regulators have authorized sales of nicotine pouches, however, the agency stressed that no nicotine products are safe and are not considered “FDA approved.” Marketing for ...