Investigational·5 treatments

Future Treatments

Drugs in late-stage clinical trials that are not yet approved for use. Early data is promising — but Phase 3 trial results and regulatory decisions may differ from earlier trials.

Quick read · 3 min

Investigational — not yet approved

This treatment is in clinical trials and has not been approved by the FDA or any regulatory authority. It is not available for prescription.

In simple terms:
  • 5 drugs are in late-stage trials for obesity — none are approved yet
  • These trials are ongoing — trial results and approval timelines can change
  • The most advanced (Orforglipron) has an FDA decision expected in 2026 — the rest are 2027 or later
  • All estimated approval dates on this page are not confirmed

Based on clinical trials · No rankings · Every claim linked to source

Last reviewed: March 2026

At a glance

DrugBest trial result
Retatrutide
Eli Lilly
up to 28.7%
Phase 2 randomised controlled trial (NEJM 2023)
CagriSema
Novo Nordisk
up to 22.7%
REDEFINE 1
Amycretin
Novo Nordisk
up to 22%
Phase 1b/2a randomised controlled trial (subcutaneous)
MariTide
Amgen
up to 20%
Phase 2 randomised dose-finding study
Orforglipron
Eli Lilly
up to 12.4%
ATTAIN-1

All future treatments

Retatrutide

Phase 3
Triple agonist (GIP + GLP-1 + Glucagon)
up to 28.7%
average weight loss — Phase 2 randomised controlled trial (NEJM 2023)

A triple GIP, GLP-1, and glucagon receptor agonist. The first Phase 3 result (TRIUMPH-4, 2026) showed 28.7% average weight loss at 68 weeks — the highest weight loss ever recorded in a Phase 3 randomised controlled trial. The addition of glucagon receptor agonism on top of GIP and GLP-1 may further boost metabolic rate and fat burning beyond what dual agonists achieve.

FormOnce-weekly subcutaneous injection (investigational — doses 9 mg and 12 mg in Phase 3)
Approval2027 (estimated — not confirmed)
Full details →

Orforglipron

Phase 3
Oral GLP-1 agonist (pill)
up to 12.4%
average weight loss — ATTAIN-1

A small-molecule oral GLP-1 receptor agonist that has completed Phase 3 trials for obesity. The FDA NDA is currently under review with a PDUFA decision date of April 10, 2026. Oral Wegovy (semaglutide pill) was the first oral GLP-1 approved for weight loss (December 2025) — orforglipron's key differentiator is that unlike oral Wegovy, it has NO food or water restrictions. You can take it any time without planning around meals.

FormOnce-daily oral tablet — no food or water restrictions (investigational)
ApprovalApril 2026 (FDA decision expected April 10, 2026 — not yet confirmed)
Full details →

CagriSema

Phase 3
GLP-1 + Amylin agonist
up to 22.7%
average weight loss — REDEFINE 1

A fixed-dose combination of cagrilintide (a long-acting amylin analogue) and semaglutide 2.4 mg in a single weekly injection. Amylin is a hormone co-secreted with insulin that reduces appetite and slows gastric emptying — complementing GLP-1 action through a different pathway.

FormOnce-weekly subcutaneous injection (fixed-dose combination, investigational)
Approval2026–2027 (estimated — not confirmed)
Full details →

Amycretin

Phase 3
GLP-1 + Amylin agonist
up to 22%
average weight loss — Phase 1b/2a randomised controlled trial (subcutaneous)

A single unimolecular drug that activates both GLP-1 and amylin receptors — hitting the same two targets as CagriSema but in a single molecule rather than two separate drugs combined. Both a weekly injection and a daily pill are being developed. Early data shows exceptional promise, with oral Phase 1 results exceeding oral semaglutide.

FormOnce-weekly subcutaneous injection AND once-daily oral pill (both formulations in development)
Approval2028+ (estimated — not confirmed)
Full details →

MariTide

Phase 3
GIP antagonist + GLP-1 agonist
up to 20%
average weight loss — Phase 2 randomised dose-finding study

MariTide takes a completely different approach to other weight loss drugs. While tirzepatide activates the GIP receptor, MariTide blocks it — using the opposite strategy — while also activating GLP-1. This antibody-peptide conjugate (a different drug class entirely from small molecules or peptide injections) only needs to be injected once a month or less, which could be transformative for adherence.

FormOnce-monthly injection under the skin (or less frequent — still being determined in Phase 3)
Approval2027+ (estimated — not confirmed)
Full details →
Important: These drugs have not been approved by any regulatory authority. Trial results — particularly from Phase 2 studies — may not predict Phase 3 outcomes. Expected approval dates are estimates and subject to change. Do not seek these drugs outside of clinical trials.

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