10 Innovations That Changed Weight Loss (2016 to 2026)

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What's new

Ten weight-loss innovations from 2016 to 2026, listed by date: the new food label, Plenity, Imcivree, Wegovy, endoscopic sleeve, Zepbound, heart protection, OTC glucose monitors, new indications and GLP-1 pills. Checked October 7, 2026.

Fact-checked against FDA labels and official sources; not yet reviewed by a licensed clinician. This page is education, not medical advice. Talk to your doctor before starting, stopping or changing any treatment.

Key takeaways

  • Wegovy (approved June 4, 2021) led to 14.9% average weight loss vs 2.4% on placebo in STEP 1.[8]
  • Zepbound (approved November 8, 2023) led to up to 20.9% vs 3.1% in SURMOUNT-1.[16]
  • SELECT showed a 20% lower risk of heart attack, stroke or cardiovascular death with semaglutide, leading to a heart indication in March 2024.[17]
  • The first over-the-counter glucose monitor was cleared on March 5, 2024; its value for weight loss is unproven.[19]
  • Two GLP-1 weight-loss pills were approved: Wegovy tablets (December 22, 2025) and Foundayo (April 1, 2026).[25]

In short: In ten years, weight loss changed more than in the half century before. The biggest shift was a new generation of medicines: semaglutide (Wegovy, 2021) and tirzepatide (Zepbound, 2023) brought average losses of about 15% to 21% in their main trials, then proved benefits for the heart, sleep apnea and liver disease, and in 2025 and 2026 arrived as daily pills. Around them came a clearer food label, a medicine for rare genetic obesity, a stomach-stitching procedure done without incisions, and glucose monitors sold over the counter. Here are ten milestones, listed by date, not ranked, with what each changed and what it did not. Checked on October 7, 2026.

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For where these options fit today, see every FDA-approved weight-loss medication compared or answer a few questions in Find My Options. For the longer story, from 1860s diets to fen-phen, read our history of weight loss.

A decade in numbers

  • 2.4 to 14.9%average weight loss on placebo vs semaglutide 2.4 mg in STEP 1 (68 weeks)NEJM 2021
  • 20.9%average loss on tirzepatide 15 mg in SURMOUNT-1 (72 weeks)NEJM 2022
  • 20%lower risk of heart attack, stroke or cardiovascular death with semaglutide in SELECT (hazard ratio 0.80)NEJM 2023
  • 2GLP-1 weight-loss pills approved, December 2025 and April 2026Drugs@FDA

Checked on October 7, 2026

1. 2016: A Nutrition Facts label built around calories

In 2016 the FDA finalized the first major redesign of the Nutrition Facts label in more than two decades. Calories, servings per container and serving size got larger, bold type; “added sugars” appeared in grams and as a percent Daily Value; and serving sizes were updated to reflect what people actually eat (a serving of ice cream went from half a cup to two-thirds, a soda from 8 to 12 ounces). Large manufacturers had to switch by January 1, 2020, and smaller ones by January 1, 2021. Why it mattered: it made the single number most people track easier to find and harder to shrink with tiny serving sizes. What it didn’t do: labels inform; they don’t change appetite. Our calorie deficit guide explains how to use them.

2. 2019: A swallowable hydrogel for fullness

On April 12, 2019, the FDA authorized Plenity through its De Novo pathway, as a prescription aid for weight management in adults with a BMI of 25 to 40 alongside diet and exercise. The capsules release particles of a cellulose-and-citric-acid hydrogel that swell in the stomach to add a feeling of fullness. Why it mattered: it was a new kind of option, a device taken by mouth rather than a drug or a procedure. What it didn’t do: commercial staying power; its maker, Gelesis, filed for Chapter 7 liquidation in October 2023. Our procedures hub covers the devices and procedures that remain.

3. 2020: The first medicine for rare genetic obesity

On November 25, 2020, the FDA approved Imcivree (setmelanotide) for obesity caused by three rare genetic conditions (POMC, PCSK1 or LEPR deficiency) confirmed by genetic testing. It was later approved for Bardet-Biedl syndrome (2022) and, on March 19, 2026, for acquired hypothalamic obesity. Why it mattered: it was the first weight medicine aimed at a specific biological cause, and it underlined that some obesity is driven by identifiable defects in the brain’s appetite pathway. What it didn’t do: it is not a general weight-loss medicine; it works only in the conditions on its label.

4. 2021: Wegovy and the new era of GLP-1 medicines

On June 4, 2021, the FDA approved Wegovy (semaglutide 2.4 mg) for chronic weight management. In the STEP 1 trial, 1,961 adults lost an average of 14.9% of their body weight over 68 weeks, compared with 2.4% on placebo, and 86.4% lost at least 5%. Why it mattered: for comparison, daily liraglutide (Saxenda) averaged 7.4% vs 3.0% in its 56-week label trial, a separate study; Wegovy’s results put GLP-1 medicines at the center of obesity care. Our GLP-1 medications guide explains how they work. What it didn’t do: it isn’t a short course. In the STEP 1 extension, about two-thirds of the lost weight came back within a year of stopping.

5. 2022: Endoscopic sleeve gastroplasty gets its own authorization

On July 12, 2022, the FDA granted De Novo authorization to the Apollo ESG system, an endoscopic suturing device that folds and stitches the stomach into a narrower sleeve from the inside, with no incisions, for adults with a BMI of 30 to 50. In the MERIT randomized trial of 209 adults, published in The Lancet in 2022, total weight loss at 52 weeks was 13.6% with endoscopic sleeve gastroplasty plus lifestyle changes vs 0.8% with lifestyle changes alone, with serious adverse events in 2%. Why it mattered: it opened a middle path between medicines and surgery. What it didn’t do: match surgery; in comparisons, typical losses are smaller than with a sleeve gastrectomy. Our bariatric surgery guide covers the surgical options.

6. 2023: Zepbound and the dual agonist

On November 8, 2023, the FDA approved Zepbound (tirzepatide), which acts on both GIP and GLP-1 receptors. In SURMOUNT-1, published in 2022, 2,539 adults lost an average of 15.0%, 19.5% and 20.9% on the 5, 10 and 15 mg doses over 72 weeks, vs 3.1% on placebo. Why it mattered: it was the first approved weight medicine to act on two hormone pathways at once, and several drugs now in trials combine even more (see “On the horizon” below). What it didn’t do: end the cost problem; access still depends heavily on insurance and price. See our semaglutide vs tirzepatide comparison.

Average weight loss in landmark trials (not head-to-head)Values in %
Average weight loss in landmark trials (not head-to-head)
ItemTreatmentPlacebo or control
Wegovy, STEP 1 (68 wk)14.9%2.4%
Zepbound 15 mg, SURMOUNT-1 (72 wk)20.9%3.1%
ESG, MERIT (52 wk)13.6%0.8%
Wegovy tablets, label trial (64 wk)13.6%2.4%
Foundayo, label trial (72 wk)11.1%2.1%

Chronological. Separate trials with different people, lengths and comparison groups; not a ranking. Bars show percent of body weight lost.

Source: NEJM 2021 and 2022; The Lancet 2022 (MERIT); FDA labels on DailyMed (checked on October 7, 2026)

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7. 2023-2024: Proof that weight medicines protect the heart

The SELECT trial, published in November 2023, followed 17,604 adults with overweight or obesity and established cardiovascular disease, but without diabetes, for an average of 39.8 months. Heart attack, stroke or cardiovascular death occurred in 6.5% of those on semaglutide vs 8.0% on placebo, a 20% lower risk. On March 8, 2024, the FDA approved Wegovy to reduce the risk of these events in adults with cardiovascular disease and obesity or overweight, the first weight medicine with that indication. Why it mattered: it was the first time a weight-loss medicine was shown in a large outcomes trial to reduce heart attacks, strokes and cardiovascular deaths. What it didn’t do: apply to everyone; the indication is for people with established heart disease.

8. 2024: Glucose monitors go over the counter

On March 5, 2024, the FDA cleared the first over-the-counter continuous glucose monitor, for adults who do not use insulin, including people without diabetes who want to see how food and exercise affect their glucose. Others followed later that year. Why it mattered: it put a once-specialist tool in consumers’ hands and fed a wave of personalized-nutrition apps. What it didn’t do: prove itself for weight loss; pooled studies in people without diabetes show no significant effect on BMI. Our explainer on CGMs for weight loss without diabetes covers the evidence, and a related tracking trend is checked in AI calorie counting from photos.

9. 2024-2025: Treating the conditions that come with weight

On December 20, 2024, the FDA approved Zepbound for moderate-to-severe obstructive sleep apnea in adults with obesity, the first medicine for that condition. On August 15, 2025, Wegovy received accelerated approval for metabolic dysfunction-associated steatohepatitis (MASH) with moderate to advanced liver fibrosis. Why it mattered: weight medicines started to be approved for diseases linked to excess weight, which can also open other coverage routes; for example, Medicare drug plans can cover Zepbound for sleep apnea. Our guides to sleep apnea and weight and fatty liver and weight explain both. What it didn’t do: replace other treatments; CPAP and liver care still matter.

10. 2025-2026: GLP-1 pills, a higher dose and new ways to pay

On December 22, 2025, the FDA approved Wegovy tablets (oral semaglutide 25 mg) for weight management, with average weight change of -13.6% vs -2.4% at 64 weeks in the label trial. On April 1, 2026, it approved Foundayo (orforglipron), a small-molecule daily pill that can be taken with or without food (-11.1% vs -2.1% at 72 weeks on the highest dose). In between, on March 19, 2026, came a 7.2 mg dose, Wegovy HD. At the same time, makers began selling direct at lower self-pay prices, from about $149 a month for the lowest pill strengths as of October 2026, and the Medicare GLP-1 Bridge began on July 1, 2026, with a $50 copay for people who meet its criteria. Why it mattered: no needles, and for many people, a real price. What it didn’t do: make the medicines right for everyone, or remove the need to keep taking them. Our oral GLP-1 guide, insurance guide and cost hub have the details.

The decade at a glance

DateInnovationType
2016New Nutrition Facts label finalized (on most foods by 2020-2021)Food labeling
April 12, 2019Plenity hydrogel authorized (De Novo); maker liquidated in 2023Device
November 25, 2020Imcivree approved for rare genetic obesityMedicine
June 4, 2021Wegovy approved (STEP 1: -14.9% vs -2.4%)Medicine
July 12, 2022Endoscopic sleeve gastroplasty device authorized (De Novo)Procedure
November 8, 2023Zepbound approved (SURMOUNT-1: up to -20.9% vs -3.1%)Medicine
March 5, 2024First over-the-counter CGM clearedDevice
March 8, 2024Wegovy approved to reduce cardiovascular risk (SELECT)Medicine
December 20, 2024Zepbound approved for obstructive sleep apneaMedicine
August 15, 2025Wegovy accelerated approval for MASHMedicine
December 22, 2025Wegovy tablets approvedMedicine
March 19, 2026Wegovy HD (7.2 mg) approvedMedicine
April 1, 2026Foundayo (orforglipron) approvedMedicine
July 1, 2026Medicare GLP-1 Bridge begins ($50 copay)Access
Chronological; not a ranking. Sources: Drugs@FDA, FDA approval letters and press releases, FDA device databases, CMS, SEC filing (Gelesis), checked 2026-10-07.

What did not change

Every one of these innovations still sits on the same foundation. All the medicine labels pair treatment with a reduced-calorie diet and more physical activity. Strength training and enough protein remain the main ways to protect muscle while losing weight, as our guide to muscle loss on GLP-1s explains. And keeping weight off still takes ongoing effort, with or without medicine; our maintenance guide covers what helps.

On the horizon (investigational)

We follow these in our retatrutide results explainer, CagriSema explainer, the article on muscle-preserving weight-loss drugs and the emerging medications tracker. For this year’s developments in one place, see what’s new in weight loss in 2026.

Using this history to make your own choices

  1. Start with what is approvedCheck which options have an FDA label for your situation.
  2. Look at the trial, not the headlineWho was studied, for how long, and compared with what.
  3. Count the full costPrice, coverage and how long you would need to stay on it.
  4. Ask about the basics tooDiet, activity and sleep still shape results with any treatment.
  5. Talk it throughBring your questions to a clinician, using our tools to prepare.

Our tools, including the BMI, calorie and protein calculators, can help you prepare for that conversation, and the printable questions to ask before starting a GLP-1 is a good next step if a medicine is on your list. For the story of the drugs that came before this decade, see our history of weight-loss drugs.

Records in this article

Related guides

Questions to ask a professional

  • Which of the newer options are approved for my situation?
  • Would a pill, a weekly injection or a procedure fit my health and routine best?
  • What would treatment cost me with my coverage, and for how long?
  • What should I do alongside any treatment to protect muscle and keep weight off?

Frequently asked questions

What were the main weight-loss innovations of the last 10 years?

We list innovations by date rather than ranking them. Among them, GLP-1-based medicines, starting with Wegovy in 2021 and Zepbound in 2023, brought average losses of about 15% to 21% in their main trials and later showed heart, sleep apnea and liver benefits.

When was Wegovy approved for weight loss?

June 4, 2021. A heart-risk indication followed on March 8, 2024, the tablets on December 22, 2025, and a 7.2 mg dose (Wegovy HD) on March 19, 2026.

Is there a weight-loss pill now?

Yes. Wegovy tablets (oral semaglutide) were approved on December 22, 2025, and Foundayo (orforglipron) on April 1, 2026. Older pills, such as phentermine and Qsymia, have been available for longer.

What weight-loss treatments are coming next?

Investigational options include retatrutide, CagriSema and muscle-preserving drugs. None is FDA approved for weight management as of October 7, 2026.

Do these innovations replace diet and exercise?

No. Every medicine label pairs treatment with a reduced-calorie diet and more activity, and strength training and protein help protect muscle.

References

  1. Changes to the Nutrition Facts Label (2016 final rule; compliance dates). U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  2. De Novo classification request for Plenity (DEN180060). U.S. Food and Drug Administration, 2019. (accessed October 7, 2026) Government page
  3. Gelesis Holdings, Inc. Form 8-K: voluntary petition under Chapter 7 (October 30, 2023). U.S. Securities and Exchange Commission (EDGAR), 2023. (accessed October 7, 2026) Government page
  4. Imcivree (setmelanotide) approval letter, NDA 213793 (2020-11-25). U.S. Food and Drug Administration, 2020. (accessed October 7, 2026) Government page
  5. NDA 213793/S-001 approval letter (Bardet-Biedl syndrome). U.S. Food and Drug Administration, 2022. (accessed October 7, 2026) Government page
  6. NDA 213793/S-009 approval letter (acquired hypothalamic obesity). U.S. Food and Drug Administration, 2026. (accessed October 7, 2026) Government page
  7. Drugs@FDA: Wegovy, NDA 215256, approval history. U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  8. Wilding JPH, Batterham RL, Calanna S, et al.. Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1). New England Journal of Medicine, 2021. doi:10.1056/NEJMoa2032183 · PMID 33567185 · NCT03548935 (accessed October 7, 2026) Randomized trial
  9. Wilding JPH, Batterham RL, Davies M, et al.. Weight regain and cardiometabolic effects after withdrawal of semaglutide: The STEP 1 trial extension. Diabetes, Obesity and Metabolism, 2022. doi:10.1111/dom.14725 · PMID 35441470 (accessed October 7, 2026) Randomized trial
  10. De Novo DEN210045: APOLLO ESG, ESG SX, REVISE and REVISE SX Systems. U.S. Food and Drug Administration, 2022. (accessed October 7, 2026) Government page
  11. Abu Dayyeh BK, et al.. Endoscopic sleeve gastroplasty for treatment of class 1 and 2 obesity (MERIT): a prospective, multicentre, randomised trial. The Lancet, 2022. doi:10.1016/S0140-6736(22)01280-6 · PMID 35908555 (accessed October 7, 2026) Randomized trial
  12. Sleeve Gastrectomy Shows Advantages over Endoscopic Sleeve Gastroplasty (ACS Brief, on Leslie ZD et al., J Am Coll Surg 2026). American College of Surgeons, 2026. (accessed October 7, 2026) News (reported facts only)
  13. Drugs@FDA: Saxenda, NDA 206321 (original approval 2014-12-23). U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  14. Abbott Receives U.S. FDA Clearance for Two New Over-the-Counter Continuous Glucose Monitoring Systems (Lingo and Libre Rio). Abbott (press release), 2024. (accessed October 7, 2026) News (reported facts only)
  15. Drugs@FDA: Zepbound, NDA 217806. U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  16. Jastreboff AM, Aronne LJ, Ahmad NN, et al.. Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1). New England Journal of Medicine, 2022. doi:10.1056/NEJMoa2206038 · PMID 35658024 · NCT04184622 (accessed October 7, 2026) Randomized trial
  17. Lincoff AM, Brown-Frandsen K, Colhoun HM, et al.. Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes (SELECT). New England Journal of Medicine, 2023. doi:10.1056/NEJMoa2307563 · PMID 37952131 · NCT03574597 (accessed October 7, 2026) Randomized trial
  18. FDA Approves First Treatment to Reduce Risk of Serious Heart Problems Specifically in Adults with Obesity or Overweight. U.S. Food and Drug Administration, 2024. (accessed October 7, 2026) Government page
  19. FDA Clears First Over-the-Counter Continuous Glucose Monitor. U.S. Food and Drug Administration, 2024. (accessed October 7, 2026) Government page
  20. Liao X, Li Y, Tang S, et al.. Continuous glucose monitoring in non-diabetic populations: a systematic review of observational and interventional studies with meta-analysis. European Journal of Medical Research, 2026. doi:10.1186/s40001-026-03920-0 · PMID 41588451 (accessed October 7, 2026) Meta-analysis
  21. FDA Approves First Medication for Obstructive Sleep Apnea. U.S. Food and Drug Administration, 2024. (accessed October 7, 2026) Government page
  22. NDA 215256/S-024 accelerated approval letter (MASH). U.S. Food and Drug Administration, 2025. (accessed October 7, 2026) Government page
  23. Drugs@FDA: Wegovy tablets, NDA 218316. U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  24. NDA 215256/S-029 and NDA 218316/S-005 approval letter (Wegovy injection 7.2 mg weekly dose). U.S. Food and Drug Administration, 2026. (accessed October 7, 2026) Government page
  25. Drugs@FDA: Foundayo, NDA 220934. U.S. Food and Drug Administration. (accessed October 7, 2026) Government page
  26. WEGOVY (semaglutide) injection and tablets: prescribing information. Novo Nordisk, via DailyMed, 2026. (accessed October 7, 2026) Drug label
  27. FOUNDAYO (orforglipron) tablets: prescribing information. Eli Lilly and Company, via DailyMed, 2026. (accessed October 7, 2026) Drug label
  28. Wegovy at NovoCare Pharmacy: self-pay prices. Novo Nordisk (NovoCare Pharmacy). (accessed October 7, 2026) Other
  29. Medicare GLP-1 Bridge: information for providers. Centers for Medicare and Medicaid Services. (accessed October 7, 2026) Government page

Facts checked on October 7, 2026

Educational information, not medical advice. Talk with a qualified healthcare professional about your own situation. In an emergency call 911.

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