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		Eli Lilly obesity drug data shines, shares rise
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		 [April 29, 2022] 
		By Mrinalika Roy and Leroy Leo 
 (Reuters) -Eli Lilly and Co on Thursday 
		said its potential blockbuster obesity drug achieved a goal of helping 
		patients lose more than 20% of their weight in a late-stage clinical 
		trial, and its shares rose about 3%.
 
 The U.S. drugmaker also reported first-quarter earnings that topped Wall 
		Street estimates.
 
 The drug, tirzepatide, which is also being studied as a treatment for 
		type 2 diabetes, demonstrated up to 22.5% weight loss in adults with 
		obesity.
 
 "The data likely validates Street thinking that tirzepatide will become 
		a dominant player in the obesity market," Wells Fargo analyst Mohit 
		Bansal said in a note, adding that he expects about $4 billion in peak 
		sales.
 
 Mizuho Securities analyst Vamil Divan said the drug "has potential to be 
		a multibillion-dollar product" for both diabetes and weight loss.
 
 Additionally, the company said it expects to complete initial submission 
		of data on its experimental Alzheimer's treatment, donanemab, to the 
		U.S. Food & Drug Administration in the current quarter as it seeks 
		accelerated approval.
 
 Lilly in February pushed back its timeline to complete the donanemab 
		application to sometime later in 2022 from the first quarter in light of 
		a U.S. proposal that would severely limit Medicare coverage for drugs in 
		its class.
 
 In April, the U.S. Centers for Medicare & Medicaid Services (CMS) 
		decided to allow standard reimbursement only for Alzheimer's drugs 
		approved under the traditional FDA process based clear proof of patient 
		benefit, rather than removal of brain plagues or other secondary goals 
		that might slow cognitive decline.
 
 
		
		 
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			A sign is pictured outside an Eli Lilly and Company pharmaceutical 
			manufacturing plant at 50 ImClone Drive in Branchburg, New Jersey, 
			March 5, 2021. Picture taken March 5, 2021. REUTERS/Mike Segar/File 
			Photo 
            
			 The decision came after a 
			controversial accelerated approval for Biogen Inc's similar 
			Alzheimer's drug Aduhelm.
 Lilly expects a decision from the FDA on donanemab in early 2023, 
			which would be close to when data will be available from its 
			late-stage study, Chief Scientific Officer Daniel Skovronsky said.
 He added that the company believes the timing 
			"would enable parallel discussions with CMS regarding outright 
			coverage and expedited review time for full FDA approval."
 Still, Mizuho's Divan said, "there's almost no expectations for 
			sales from donanemab this year or next year, just given the 
			challenges that Biogen had on the reimbursement side."
 
 Lilly reported adjusted first-quarter earnings of $2.77 per share, 
			topping analysts' estimates of $2.32, according to IBES data from 
			Refinitiv.
 
 It now sees full-year adjusted earnings of $8.15 to $8.30 per share, 
			down from its prior forecast of $8.50 to $8.65 per share, in part 
			due to accounting changes in how it reports results.
 
 (Reporting by Mrinalika Roy and Leroy Leo in Bengaluru; Editing by 
			Amy Caren Daniel and Bill Berkrot)
 
 
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