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M&A, Deals, Partnerships: Sanofi completes acquisition of Inhibrx Biosciences, Inc. (San Diego), enhancing its rare disease pipeline with SAR447537, a promising treatment for alpha-1 antitrypsin deficiency (AATD). Inhibrx shareholders approved the acquisition, valued at approximately $1.7 billion. Biotech M&A slumps as drugmakers take a break from public deals. After defying the biggest dealmaking downturn in a decade, Big Pharma is taking a little breather from chasing public companies in favor of smaller, private targets. Drugmakers including Bristol Myers Squibb and AbbVie spent heavily on targets during the later months of last year, often paying hefty premiums in a bid to refresh aging portfolios with new blockbuster medicines. - Sector transaction values cool off after hot streak in 2023 - Big Pharma switches to private deals, with activity up 198% - The value of biotech deals down by more than 40% year-on-year to about $40 billion. IPOs:  Rapport Therapeutics (Boston & SD) announces pricing of IPO. Rapport is a #clinical-stage #biotechnology company focused on discovery and development of transformational small molecule medicines for patients suffering from central nervous system disorders. Rapport announced the pricing of its initial public offering of 8,000,000 shares of its common stock at a public offering price of $17.00 per share. Alumis (South SF) readies IPO to fund rival drug to Bristol Myers Squibb's SOTYKTU™ (deucravacitinib) US HCP. Biotechnology startup Alumis outlined plans for an initial public offering that would fund clinical development of a pair of #autoimmune and #neurological disease drugs. Both medicines are TYK2 inhibitors, a group of oral medicines that drugmakers are positioning as alternatives to injectable #biologics for #inflammatory conditions. FDA Approvals: Eli Lilly and Company Alzheimer’s drug gets unanimous backing of FDA panel. An experimental and closely watched medicine for #Alzheimer’s disease is one step closer to approval, after receiving support from a panel of experts who advise the Food and Drug Administration. The panel unanimously voted that the medicine, developed known as #donanemab, appears to be an effective treatment for certain Alzheimer’s patients. The experts also concluded, by an 11-0 vote, that the drug’s benefits outweigh its risks, despite some safety concerns. Should the agency grant approval, donanemab would be the third Alzheimer’s therapy of its kind cleared for the U.S. market. These medicines work by breaking up sticky, toxic collections of “amyloid beta,” a protein many researchers believe to be a root cause of the memory-robbing disease.

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