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    3. >Lilly gets a boost from new weight-loss pill data as it weighs speedier approval in US
    Headlines

    Lilly Gets a Boost From New Weight-Loss Pill Data as It Weighs Speedier Approval in US

    Published by Global Banking & Finance Review®

    Posted on September 17, 2025

    3 min read

    Last updated: January 21, 2026

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    Tags:innovationhealthcarefinancial servicesinvestmentinsurance

    Quick Summary

    Eli Lilly's weight-loss pill orforglipron shows promising trial results, boosting its approval chances in the competitive GLP-1 market.

    Eli Lilly Gains Momentum with New Data on Weight-Loss Pill Approval

    By Maggie Fick and Mrinalika Roy

    VIENNA (Reuters) - Eli Lilly's bid for approval for an experimental weight-loss pill got a boost on Wednesday with new clinical trial data, and the company reaffirmed that it was too soon to assume the drug will be part of a new U.S. speedy review program.

    Lilly's shares rose about half a percentage point on Wednesday. Its pill, orforglipron, is designed to mimic the appetite-suppressing GLP-1 hormone targeted by the company's blockbuster injection tirzepatide, sold under the brand names Mounjaro and Zepbound.

    Lilly, based in Indianapolis, has been trying to widen its lead in the fast-growing market for GLP-1 drugs over Danish rival Novo Nordisk <NOVOb.CO>. Novo was first-to-market with GLP-1 medicines Ozempic for diabetes and Wegovy for obesity but this year ousted its CEO and its share price has dropped about 40% as competition has intensified from Lilly.

    Lilly said that in a head-to-head trial of adults with type 2 diabetes orforglipron lowered average blood sugar and weight more effectively than Novo's older GLP-1 pill Rybelsus.

    "The data strengthens our conviction that Eli Lilly is well positioned to maintain leadership in the GLP-1 market," said Daniel Barasa, portfolio manager at Gabelli Funds. He said orforglipron not only shows superior efficacy but also advantages in dosing convenience in the trial against Rybelsus.

    Full data from a different late-stage trial of the drug showed that orforglipron helped overweight people lose about 12% of their body weight, with a safety profile similar to injected drugs, Lilly said on Tuesday.

    The new data "give us increased confidence in the competitive profile of orforglipron," BMO Capital Markets analyst Evan Seigerman said in a Wednesday research note.

    Lilly, the world's most valuable drugmaker by market value, is expanding U.S. and international manufacturing capacity to meet soaring demand for GLP-1 treatments, as it races with Novo to get an oral version to the market for weight loss.

    Novo expects a U.S. regulatory decision on its oral obesity drug candidate later this year.

    Several Wall Street analysts have suggested that orforglipron could be a candidate for the U.S. Food and Drug Administration's new priority voucher that shortens reviews for certain therapies that address major public health needs, but executives at Lilly signalled caution.

    "There is very little knowledge about this national priority voucher today. I would not assume we will submit with a national priority voucher, because we do not fully understand what it contains," Patrik Jonsson, president of Lilly International, told Reuters in an interview on Wednesday.

    Kenneth Custer, president of Lilly Cardiometabolic Health, repeated the company's earlier statement that it is too early to know how the program might apply to Lilly's pipeline.

    Lilly has said it plans to seek regulatory approval of orforglipron for weight-loss this year and will file for approval of the drug as a diabetes treatment next year.

    Jonsson said Lilly plans to file for approval of orforglipron with regulators in the United States, Britain, European Union, Japan and China "within weeks" of each other.

    He declined to specify locations for pill manufacturing outside the U.S., but confirmed non-U.S. production is planned.

    The drug is forecast by analysts to generate peak annual sales as high as $10 billion. 

    (Reporting by Maggie Fick, Sriparna Roy, and Mrinalika Roy; additional reporting by Deena Beasley in Los Angeles. Editing by Mark Potter, Sharon Singleton, Chizu Nomiyama and David Gregorio)

    Key Takeaways

    • •Eli Lilly's orforglipron shows promising clinical trial results.
    • •The pill targets the GLP-1 hormone for weight loss.
    • •Lilly aims for regulatory approval in multiple regions.
    • •Orforglipron could generate $10 billion in annual sales.
    • •Lilly competes with Novo Nordisk in the GLP-1 market.

    Frequently Asked Questions about Lilly gets a boost from new weight-loss pill data as it weighs speedier approval in US

    1What is orforglipron?

    Orforglipron is an experimental weight-loss pill developed by Eli Lilly, designed to mimic the appetite-suppressing GLP-1 hormone.

    2How effective is orforglipron in clinical trials?

    In clinical trials, orforglipron helped overweight individuals lose about 12% of their body weight and lowered average blood sugar more effectively than Novo's Rybelsus.

    3What are Eli Lilly's plans for regulatory approval?

    Eli Lilly plans to seek regulatory approval for orforglipron for weight-loss this year and will file for approval as a diabetes treatment next year.

    4How does orforglipron compare to Novo Nordisk's products?

    Orforglipron has shown to be more effective in lowering blood sugar and weight compared to Novo Nordisk's older GLP-1 pill, Rybelsus.

    5What is the potential market for orforglipron?

    Analysts forecast that orforglipron could generate peak annual sales as high as $10 billion, indicating a significant market opportunity.

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