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In parts of the U.S., a push to protect and expand access to IVF

In parts of the U.S., a push to protect and expand access to IVF

Washington Post01-07-2025
State laws that protect and expand access to in vitro fertilization take effect Tuesday and in coming months as lawmakers continue working to address questions surrounding the procedure more than a year after an Alabama Supreme Court ruling muddled its legality.
In Tennessee, state law codifies the right to IVF and other fertility treatments beginning Tuesday. In Virginia, a new measure directs a health insurance commission to consider coverage plans for infertility. And in California, a law that would have taken effect Tuesday before being delayed will move the state toward requiring some group health plans to cover fertility treatments, including IVF.
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Shares of Brazil's Fleury jump on reports of talks with Rede D'Or
Shares of Brazil's Fleury jump on reports of talks with Rede D'Or

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Shares of Brazil's Fleury jump on reports of talks with Rede D'Or

SAO PAULO (Reuters) -Shares of Brazilian medical diagnostics company Fleury jumped on Monday after reports of a potential acquisition by hospital chain Rede D'Or, which analysts said could generate synergies. Fleury's shares rose more than 15% in trading in Sao Paulo, making it the biggest gainer on benchmark stock index Bovespa, which was up 0.6%. Rede D'Or, meanwhile, gained 1.2%. Multiple local media outlets said on Sunday that Rede D'Or was in talks with Fleury on a deal that could combine Brazil's largest integrated healthcare network with a leading medical lab chain. Brazil Journal reported, citing sources, that Rede D'Or was working on an offer that could include both a cash payment and share swap. Fleury counts lender Bradesco as one of its main shareholders. Rede D'Or said on Monday it continuously evaluates opportunities to expand, including potential acquisitions or business combinations, but that no decision or proposal had been made for a potential deal with Fleury. In a separate statement, Fleury said it regularly analyzes market conditions but also noted that no decision had been reached on a potential transaction with Rede D'Or. Goldman Sachs analysts said Fleury could benefit under Rede D'Or's management from better procurement terms, especially on materials, in which there would be some overlap, and a leaner general and administrative structure. Fleury has a market capitalization of 6.91 billion reais ($1.24 billion), while Rede D'Or's market cap stands at 75.29 billion reais, according to LSEG data. Rede D'Or in 2022 acquired insurer SulAmerica in a deal worth 13 billion reais, part of a trend for consolidation in Brazil's healthcare sector that saw the hospital chain as one of the most active companies in recent years. Analysts at Santander said a deal between Fleury and Rede D'Or would make sense from a strategic point of view. "Main synergies could be related to higher scale, and therefore more bargaining power to buy materials at Fleury and G&A savings," they said. ($1 = 5.5704 reais) Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Could cancer drugs be the future of Alzheimer's treatment?
Could cancer drugs be the future of Alzheimer's treatment?

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Could cancer drugs be the future of Alzheimer's treatment?

With few treatments available to stop or reverse Alzheimer's disease, scientists have turned to cancer drugs as a potential means of walking back cognitive decline. Alzheimer's cases are rising in the United States and worldwide due to an aging population, but there is no cure for the disease. Attempts to develop new treatments that slow the disease's progress, rather than lessen symptoms, have frequently failed. Only two drugs — the antibody therapies Leqembi and Kisunla — are currently approved by the Food and Drug Administration to slow the progression of early Alzheimer's, and scientists say their benefits are limited. Some pharmaceutical companies have halted or abandoned their Alzheimer's drug development programs because of unsuccessful trials. Others are trying to use existing medications, including popular weight loss drugs, to combat Alzheimer's. With that in mind, researchers at the University of California, San Francisco conducted a broad search for drugs that could be repurposed to treat the condition — in theory, reducing the time in which the drugs could be made available to patients. They scoured a database of more than 1,300 drugs of various classes, including antipsychotics, antibiotics, antifungals and chemotherapy drugs. Then, they looked at how those drugs affected gene expression. Their new study, published Monday in the journal Cell, identified two cancer drugs as the best candidates to lower Alzheimer's risk in patients. When combined, the drugs seemed to slow or reverse Alzheimer's symptoms in mice. One of the drugs is normally used to treat breast cancer, while the other is effective against colon and lung cancer. Alzheimer's disease is associated with significant changes in the way genes are expressed in the brain, leading to the increased production of certain proteins and the decreased production of others. 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Sarepta Stock Keeps Sliding as Company Rejects FDA Call to Withdraw Drug
Sarepta Stock Keeps Sliding as Company Rejects FDA Call to Withdraw Drug

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Sarepta Stock Keeps Sliding as Company Rejects FDA Call to Withdraw Drug

Key Takeaways Sarepta Therapeutics rejected the Food and Drug Administration's call to stop shipments of its muscular dystrophy drug. The FDA request came after a third patient in a Phase 1 study died while taking a similar treatment. Shares of the biopharma firm slid Monday, extending last week's Therapeutics (SRPT) shares continued to slide Monday after the biopharmaceutical firm refused a Food and Drug Administration (FDA) request to stop distributing its Elevidys treatment for muscular dystrophy. The FDA called for the halt after a third patient suffering from a form of muscular dystrophy taking a similar gene therapy to Elevidys in a Phase 1 study died of liver failure, possibly related to the drug. The news of the patient death sent shares of Sarepta plunging Friday. Elevidys has already been approved to treat both ambulatory and non-ambulatory patients with Duchenne muscular dystrophy. Sarepta voluntarily stopped shipments for non-ambulatory patients last month following a second death during the study to gauge the efficacy of the drug for Limb-Girdle muscular dystrophy. The company noted the third patient who died suffered from non-ambulant Limb-Girdle muscular dystrophy. However, Sarepta said that because its comprehensive scientific interpretation of the data 'shows no new or changed safety signals in the ambulant patient population, we will continue to ship ELEVIDYS to the ambulant population.' Sarepta said it's looking to 'continued discussions and sharing of information with FDA in order to advance our shared purpose of protecting patient safety and informed access to care." Shares of Sarepta were down about 3% in recent trading. They've lost nearly 90% of their value since the start of the year. Read the original article on Investopedia Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

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