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Albiglutide (Tanzeum)_Dosage, benefits & legal status

Also known as Tanzeum, Eperzan, GSK-716155

Published August 24, 2026 · Updated October 5, 2026

A weekly GLP-1 withdrawn from the world market because nobody bought it.

Blood sugarGLP-1 receptor agonistFDA-approved
DoseWas set by the label
FrequencyOnce weekly
RouteUnder the skin (subcutaneous)
StatusFDA-approved (withdrawn)
CycledSet by the prescription

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

See how this dose compares across the library →

01

What is Albiglutide (Tanzeum)?

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

Overview

A weekly GLP-1 that was approved, underperformed its rivals, needed mixing before each shot, and was withdrawn worldwide for commercial reasons.

The technical version

Albiglutide, a GLP-1 receptor agonist consisting of GLP-1 dimer fused to recombinant human albumin, FDA-approved 2014 as Tanzeum and marketed in Europe as Eperzan. Elimination half-life approximately 5 days. GSK announced worldwide withdrawal in 2017 for economic reasons, with supply chain stocks depleted by 2018. Published comparative analysis found lower HbA1c and weight reduction than other agents in the class.

What it's used for

A weekly injected GLP-1 for type 2 diabetes. Withdrawn from the market and no longer available.

02

How does Albiglutide (Tanzeum) work?

What it does in the body, and where.

Albiglutide is worth a page mainly as a correction to the lists that still include it.

  1. 01
    GLP-1 fused to albumin
    The molecule joins a GLP-1 sequence to human albumin, which is what gave it a half-life of several days and allowed weekly dosing.
  2. 02
    It lost on effectiveness and on convenience
    A published analysis found it lowered HbA1c and body weight less than other GLP-1 agonists. It also required reconstitution before each injection, which patients disliked.
  3. 03
    Withdrawal was commercial
    GSK announced the worldwide withdrawal in 2017 for economic reasons and remaining supply was gone by 2018. No safety signal drove the decision, which is a meaningful difference from a drug pulled for harm.
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.

  • Type 2 diabetes, while it was marketedFDA-approved
  • Anything current, since the product no longer existsnone

The published record

Research index

323

Papers and trials about Albiglutide (Tanzeum)

245 papers tagged human · 76 not reviews or lab · 32 clinical trial publications

42 registered trials · 25 with posted results

Furthest stage reached: Approved in the US, no longer sold

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In animals28
In the lab1
Reviews157
Senior author shareSpread across many groups

Evidence summary

Counted from Europe PMC indexing, not read by a person; a human tag can land on reviews, commentary or lab papers; clinical trial publications is the narrower count.

Albiglutide (Tanzeum) vial rendering
Compound field notes

At a glance

Four things to know about Albiglutide (Tanzeum)

01

Evidence

FDA-approved

02

Category

Weight loss and metabolic

03

Common vial

Varies

04

Half-life

About 5 days

04

How much, and do you cycle it?

The range, and whether you take breaks.

Was set by the label, once weekly. Set by the prescription FDA label

This is a prescription drug. Duration and schedule are set by the label and the prescriber, not by a cycling convention.

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 5 daysHuman study

Reported elimination half-life of roughly 5 days, in the range of 4 to 7, which supported weekly dosing.

Not yet traced to a primary source.

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

06

How is it given?

Dosing context and source notes.
No draw available

Supplied as a pen or prefilled syringe, so there is nothing to mix.

Label range: 30 up to 50 mg per week. GSK Label (Tanzeum)

Dosing was once weekly by subcutaneous injection after reconstitution. The product has been withdrawn worldwide and is not available.

07

How do you store it?

Before mixing, and after.

Dry powder in the freezer or fridge. Once mixed, fridge, and use within about a month.

Unmixed lyophilized Albiglutide (Tanzeum) keeps for a long time cold. Once you add water the clock starts: most reconstituted vials hold up for roughly 28 to 30 days at fridge temperature. Keep it out of light, and do not freeze it after mixing.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Who should avoid it

Check these before anything else.
  • Not applicable as a prescription, because the product has been withdrawn worldwide and is not available
  • A personal or family history of medullary thyroid carcinoma, or MEN 2, which was a labeled contraindication for this drug class
  • Anything sold under this name on the research market, which is of unverifiable origin and cannot be the withdrawn product
  • Pregnancy or breastfeeding

Stop and get help

These are emergencies. Seek care.
  • Not applicable as a prescription, because the product is not available
  • If you hold material sold under this name, treat its identity as unverified rather than assuming it is the withdrawn drug

Common effects

Expected, and usually mild.
  • Injection site reactions, reported more often than with other GLP-1 agonists
  • Nausea
  • Diarrhea

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

09

Is Albiglutide (Tanzeum) approved?

And where the numbers on this page come from.

Approved, but no longer sold in the United States. Albiglutide (Tanzeum) was approved by the FDA, and the US product has since been discontinued.

  • Approval status
    FDA-approved
  • Route
    Under the skin (subcutaneous)
  • Checked
    24 August 2026
  • Dose
    From the drug label. The manufacturer tested this range and a regulator reviewed it.
  • Vial size
    From what vendors typically list; not a recommendation.
  • Sources
    None traced yet.

What has happened recently

FDA-approved 2014 as Tanzeum for type 2 diabetes and approved in Europe as Eperzan. GSK announced withdrawal from the worldwide market in 2017 for economic reasons, and remaining stocks were depleted by 2018. The withdrawal was not driven by a safety finding. Note that the approval tier vocabulary used on this site has no state for a withdrawn drug, so this entry is tiered on its approval history and the status field carries the withdrawal.

Guides for this compound

Sources

No primary source has been traced for this compound yet. Treat everything on this page as unverified until one is. How we grade evidence

Beyond these, 323 records are indexed. Browse the records