AstraZenecaās rare disease drug Fasenra gets US regulatorās nod
The US Food and Drug Administration approved AstraZeneca Plcās Fasenra for treatment in adult patients with a rare inflammation of blood vessels.
Bharti Rana Jayshankar – Founder
She brings in more than 30 years of experience in content building, architecture, writing, editing and storytelling. Ms Jayshankar has worked in the Economic Times daily, IBT Times, Investopedia and more than a dozen content firms as a content strategist and planner.
Jay Shankar – Co-founder
He has almost three decades of experience in journalism. He has worked with national dailies such as ET, Indian Express, The Pioneer, The Hindu, Agence France Presse and Bloomberg.
The US Food and Drug Administration approved AstraZeneca Plcās Fasenra for treatment in adult patients with a rare inflammation of blood vessels.
Merck & Co., announced it has met its primary and secondary goals during the end-stage trials of its human papillomavirus (HPV) vaccine in.
Chinaās drug regulator, the National Medical Products Association, has approvedĀ AstraZeneca Plcās asthma drug.
Daiichi Sankyo will pay Merck & Co. Inc., $170 million upfront to bag commercialization and development rights of the latterās test drug for.
Japanese researchers have developed a non-invasive alternative to detect human papillomavirus by testing urine samples, a discovery that may transform cervical cancer screening.
HQ Team June 3, 2024: An antibody-drug conjugate, jointly being developed by AstraZeneca and Daiichi Sankyo, has been shown in end-stage clinical trials.
HQ Team December 13, 2023: Japanās Eisai Co., and US-based Biogen Inc., announced its Leqembi injection will be sold in Japan from Japan.
HQ Team September 25, 2023: Record-breaking heatwaves have impacted agricultural production in Japan and the East Asian nation may look at imports to.
HQ Team September 25, 2023: Eisai Co., and Biogen Inc., announced that their drug to treat Alzheimerās disease and cognitive impairment has been.
HQ Team September 19, 2023: The European Commission granted Pfizer Inc., a marketing authorisation for its once-daily oral capsule to treat hair loss.