Health News Roundup: Bayer initiates asundexian Phase III study program; Abbott restarts Similac infant formula production at Michigan facility and more

Since then, the drugs have been shown to benefit patients with chronic kidney and heart disease and prevent heart attacks.


Devdiscourse News Desk | Updated: 29-08-2022 02:33 IST | Created: 29-08-2022 02:28 IST
Health News Roundup: Bayer initiates asundexian Phase III study program; Abbott restarts Similac infant formula production at Michigan facility and more
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Following is a summary of current health news briefs.

Abbott restarts Similac infant formula production at Michigan facility

Abbott Laboratories has restarted production of its Similac infant formula at the plant in Sturgis, Michigan at the center of the U.S. baby formula shortage. Abbott, the biggest U.S. supplier of baby formula, in February recalled Similac and other infant formula products produced at the Michigan facility after reports of bacterial infections in babies who had consumed products that originated there.

Very few in the U.S. getting full monkeypox vaccine series - CDC chief

Very few people who have gotten monkeypox shots in the United States have received the second dose needed for full protection, U.S. Centers for Disease Control and Prevention (CDC) Director Rochelle Walensky said on Friday. She told a White House briefing that nearly 97% of the shots administered were first doses, and although many people are eligible for a second dose, "very few" have been given so far.

Bayer initiates asundexian Phase III study program

Germany's Bayer said on Sunday it was starting a Phase III study program to investigate the efficacy and safety of asundexian, an oral Factor XIa (FXIa) inhibitor. The drug candidate is a potential new treatment for patients with atrial fibrillation and in patients with a non-cardioembolic ischemic stroke or high-risk transient ischemic attack, Bayer said.

AstraZeneca's Farxiga cuts death risk in heart failure patients -study

AstraZeneca's blockbuster diabetes drug Farxiga led to significant reductions in the risk of hospitalisation and death in people with all types of heart failure, according to study data released on Saturday, opening the door to a substantial increase in patients who could benefit. The drug belongs to a class of medicines called SGLT2 inhibitors that were initially approved to treat type 2 diabetes. Since then, the drugs have been shown to benefit patients with chronic kidney and heart disease and prevent heart attacks.

(With inputs from agencies.)

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