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The emblem of pharmaceutical firm Novo Nordisk is displayed in entrance of its workplaces in Bagsvaerd, on the outskirts of Copenhagen, Denmark, Nov. 24, 2025.
Tom Little | Reuters
The U.S. Meals and Drug Administration on Monday accepted the first-ever GLP-1 capsule for weight problems from Wegovy maker Novo Nordisk, a landmark choice that well being consultants say may open up therapy entry to extra sufferers.
Novo Nordisk stated it expects to launch the capsule in early 2026. The Danish drugmaker stated the beginning dose of 1.5 milligrams can be out there beginning in early January in pharmacies and by way of choose telehealth suppliers for $149 per thirty days.
Novo Nordisk didn’t say how a lot increased doses of the drug would value, however stated further data on protection and financial savings choices for eligible sufferers can be out there at the moment as effectively.
Shares of Novo Nordisk gained roughly 9% in prolonged buying and selling Monday.
The approval offers Novo Nordisk a head begin over chief rival Eli Lilly, which is at present the dominant participant available in the market and is racing to launch its personal weight problems capsule. Drugs are the subsequent battleground for the 2 drugmakers, which established the booming GLP-1 area that some analysts say might be price roughly $100 billion by the 2030s.
Wall Avenue thinks there’s loads of room for tablets available in the market, with Goldman Sachs analyst saying in August that tablets may seize a 24% share — or round $22 billion — of the 2030 international weight reduction drug market.
“What we have discovered by means of years of analysis is that having an oral choice actually sort of opens up, prompts and motivates totally different segments to hunt therapy,” Dave Moore, Novo Nordisk’s govt vice chairman of U.S. operations, instructed CNBC forward of the approval. “To have that dialog with their physician to see if that is one thing that is likely to be proper for them.”
“That is what we’re enthusiastic about — to have the ability to give individuals an choice and ensure we’ve got entry and ease of entry like we’ve got been doing with our injections,” he continued.
The FDA’s approval additionally clears the capsule to be used to cut back the chance of main cardiovascular occasions, reminiscent of loss of life, coronary heart assault or stroke, in adults with weight problems and established heart problems, in keeping with Novo Nordisk. That is in step with the approval label of the corporate’s blockbuster weight reduction drug Wegovy, which shares the identical energetic ingredient, semaglutide.
The approval relies on a section three trial that adopted greater than 300 adults with weight problems however not diabetes.
In that research, a 25-milligram dose of Novo Nordisk’s oral semaglutide helped sufferers lose as much as 16.6% of their weight on common after 64 weeks, in keeping with outcomes from the trial introduced at a medical convention in 2024. That weight reduction was 13.6% when the corporate analyzed all sufferers no matter whether or not they stopped the drug.
The capsule seems to be barely simpler than an experimental oral drug from Eli Lilly, which continues to be ready for FDA approval.
However not like Novo Nordisk’s capsule, Eli Lilly’s therapy will not be a peptide remedy. Meaning it’s absorbed extra simply by the physique and doesn’t require dietary restrictions. Individuals who take Novo Nordisk’s capsule have to attend half-hour earlier than consuming or consuming every day.
Moore stated the costs of the capsule get prices nearer to what some persons are paying for unapproved, compounded variations of branded GLP-1s, a few of that are nonetheless being illegally mass marketed and offered within the U.S.
Sufferers flocked to the cheaper copycats when Ozempic and Wegovy had been in brief provide over the past two years as a consequence of skyrocketing demand, or in the event that they did not have insurance coverage protection for the expensive remedies. Throughout FDA-declared shortages, pharmacists can legally make compounded variations of brand-name drugs. However the company earlier this 12 months decided that the scarcity of semaglutide is over, barring the follow most often.
“It continues to be alarming and disturbing for us,” Moore instructed CNBC, referring to illegitimate elements which can be imported into the U.S. illegally and utilized by some compounding pharmacies to create copycat variations of GLP-1s.
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