Next Up in Obesity Drugs: A Timeline of What’s Coming to Market (2026–2028+)

New obesity drugs are expected to be approved in the US from 2026 to 2028 and beyond, offering diverse treatment options.

The fight against obesity is entering an exciting new era. With blockbuster drugs like Wegovy (semaglutide) and Zepbound (tirzepatide) already transforming weight management, pharmaceutical giants are racing to develop next-generation therapies. The pipeline includes oral alternatives, multi-targeted injectables, and novel mechanisms that could redefine obesity treatment. Here’s a breakdown of the most anticipated drugs—and when they might hit the U.S. market.


2026: The Year of Convenience and Combination Therapies

1. Orforglipron (Eli Lilly)

  • What it is: A daily oral pill that activates the GLP-1 receptor, mimicking hormones that regulate appetite and blood sugar.
  • Why it matters: As the first oral GLP-1 agonist for obesity, it could replace injectables for many patients, boosting accessibility and adherence.

2. CagriSema (Novo Nordisk)

  • What it is: A once-weekly injectable combining semaglutide (a GLP-1 agonist) with cagrilintide (an amylin analog).
  • Why it matters: This dual-action drug targets both appetite (via GLP-1) and satiety (via amylin), potentially outperforming single-mechanism drugs.

2027: Triple-Targeted Agonists Enter the Arena

1. Survodutide (Boehringer Ingelheim)

  • What it is: A weekly injectable activating GLP-1 and glucagon receptors.
  • Why it matters: Glucagon activation may boost metabolism and fat burning, complementing GLP-1’s appetite suppression.

2. Retatrutide (Eli Lilly)

  • What it is: A weekly injectable targeting three receptors—GLP-1, GIP, and glucagon.
  • Why it matters: Early trials suggest unprecedented efficacy, with participants losing up to 24% of body weight. This “triple agonist” could set a new gold standard.

2028 and Beyond: Bold Innovations and New Pathways

1. MariTide (Amgen)

  • What it is: A monthly injectable that activates GLP-1 while blocking GIP signaling—a unique approach.
  • Why it matters: Unlike drugs that stimulate GIP (like Zepbound), Amgen bets that inhibiting GIP could enhance weight loss. Early data shows promise.

2. Bimagrumab (Eli Lilly)

  • What it is: An injectable blocking myostatin, a protein that limits muscle growth.
  • Why it matters: It could help patients lose fat while preserving or increasing muscle mass—a game-changer for metabolic health and physical function.

3. Monlunabant (Novo Nordisk)

  • What it is: A daily oral CB1 cannabinoid receptor inhibitor.
  • Why it matters: Earlier CB1 drugs (like rimonabant) were shelved for psychiatric side effects, but Monlunabant aims to target receptors outside the brain, reducing risks.
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The Bigger Picture: Trends to Watch

  1. Oral Options: Pills like Orforglipron and Monlunabant could democratize access to obesity care.
  2. Multi-Targeted Therapies: Drugs like Retatrutide and CagriSema highlight the shift toward combining hormonal pathways for amplified effects.
  3. Beyond GLP-1: Innovations like myostatin inhibition (Bimagrumab) or CB1 modulation (Monlunabant) explore entirely new biological pathways.

A Word of Caution

While these timelines reflect current estimates, approval dates may shift based on clinical trial results or regulatory reviews. Safety and long-term outcomes remain critical hurdles. Still, the diversity of approaches signals hope for personalized obesity treatments—pairing medication with lifestyle changes to tackle this complex condition.

Stay tuned: The next decade could reshape how we think about weight management, one breakthrough at a time.

—Follow for updates as these therapies progress through clinical trials and FDA review.

Reference: Nature

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