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Danuglipron_Dosage, benefits & legal status

Also known as PF-06882961

Published July 22, 2026 · Updated July 25, 2026

An experimental weight-loss pill whose development was stopped over a liver-injury signal.

Weight loss (oral)Oral GLP-1 (small molecule)Investigational
Dose40 up to 200 mg per dose
FrequencyDaily
RouteBy mouth (oral)
StatusInvestigational
CycledNo schedule. Development stopped in April 2025

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

01

What is Danuglipron?

Plain language first. The technical label stays, but it never stands alone.

Overview

It gives GLP-1-style appetite control without injections. It is in testing.

The technical version

Danuglipron is an oral GLP-1 receptor agonist and a small molecule, not a peptide, so it works as a pill.

What it's used for

An experimental appetite-lowering pill for weight loss, no needles. It is in testing.

02

How does Danuglipron work?

What it does in the body, and where.

Danuglipron was an attempt at an oral GLP-1 pill using a small molecule rather than a peptide. Development stopped.

  1. 01
    It activated the GLP-1 receptor as a small molecule
    The same approach that orforglipron went on to succeed with.
  2. 02
    Development was halted in April 2025
    Pfizer stopped the programme after a participant showed signs of drug-induced liver injury, which resolved when the drug was withdrawn.
  3. 03
    It is here for reference, not as an option
    The dose figures on this page are historical. This is not something you can obtain or should be seeking.
Receptors
HITSGLP-11

Acts on one receptor.

03

What else is it used for?

Each use below carries its own evidence level. Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

  • Weight loss without injections. Development was discontinued in 2025, so nothing is approved or availableResearch only

The published record

Research index

73

Records indexed for Danuglipron

53 in humans, 25 of them original studies.

20 registered trials, 11 with posted results.

Browse the records

In animalsPro
In the labPro
ReviewsPro
Senior author sharePro

Counted from Europe PMC indexing, not read by a person. Human means indexed under humans, which includes reviews and work on human cells. Original studies exclude reviews and lab work on human cells.Last updated 12 September 2026.

Danuglipron vial rendering
Compound field notes

At a glance

Four things to know about Danuglipron

01

Evidence

Investigational

02

Category

Weight loss and metabolic

03

Common vial

Varies

04

Half-life

About 8 hours

04

How much, and do you cycle it?

The range, and whether you take breaks.

40 up to 200 mg per dose, daily. No schedule. Development stopped in April 2025Discontinued

Pfizer ended the programme after a case of possible drug-induced liver injury, following the same fate as its sister compound the year before. Nothing about its dosing is worth planning around.

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

About 8 hoursTrial protocol

Measured in participants with normal kidney function. A twice-daily oral small molecule rather than a peptide.

Source: NCT04616027 posted results. Saxena AR, et al. Nat Med 2021;27:1079-1087

You can compare this against the whole library to see where it sits.

06

What does it cost?

Typical dose and cost, in plain numbers.

Danuglipron is not injected

It is taken by mouth (oral). Phase 2b used 40 to 200 mg twice daily. Pfizer stopped development in April 2025 after a participant showed signs of liver injury, so this is a historical dose, not an option.

Cost per month
Cost per dose
Typical dose
40 mg–200 mg / doseDiscontinued
07

How do you store it?

Before mixing, and after.

Room temperature. Cool, dry, out of light.

Danuglipron is taken as a pill or capsule. Keep it in its original container at room temperature, away from heat, humidity, and direct sun. No fridge or mixing needed. Check the expiration date on the bottle.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Who should avoid it

Check these before anything else.
  • Development has stopped, so it is not available and no prescriber is assessing anyone for it

Stop and get help

These are emergencies. Seek care.
  • Yellowing of the skin or eyes, dark urine, or severe unexplained tiredness, which can signal liver injury
  • Signs of an allergic reaction such as face or throat swelling, hives, or trouble breathing

Common effects

Expected, and usually mild.
  • Nausea, vomiting, and diarrhea, which were severe enough in the earlier twice-daily version that more than half of participants stopped taking it

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is Danuglipron approved?

And where the numbers on this page come from.

No. Danuglipron is not approved anywhere and is currently in company-run clinical trials. There is no legal route to obtain it outside a trial.

  • Approval status
    Investigational
  • Route
    By mouth (oral)
  • Checked
    September 2026

What has happened recently

Pfizer discontinued danuglipron in April 2025. One participant experienced a possible drug-induced liver injury, which resolved after stopping. An earlier twice-daily version had already been dropped in 2023 over how badly people tolerated it.

You can compare this against the whole library, or read how to check a seller.


Guides for this compound

Sources

Last reviewed 8 September 2026

Beyond these, 73 records are indexed. Browse the records