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GZC8072_Dosage, benefits & legal status

Published October 12, 2026

An experimental weekly GLP-1 pill from China, made from a modified GLP-1 peptide, with no human results yet.

Weight lossOral GLP-1 agonist (peptide)Investigational
DoseNo dose disclosed
FrequencyWeekly (intended)
RouteBy mouth (tablet)
StatusInvestigational
CycledNo established pattern

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 GZC8072?

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

Overview

Oral semaglutide is a daily peptide pill and orforglipron is a daily non-peptide pill; this aims for a weekly peptide tablet, using two in-house platforms for long action and gut absorption that the company has not described. A phase 1 in China started in September 2026. Its structure, doses and animal data are undisclosed, and it is not approved anywhere.

The technical version

GZC8072 is an oral peptide GLP-1 receptor agonist from Gan & Lee Pharmaceuticals, based on native GLP-1 and designed to be taken once a week.

What it's used for

An experimental once-weekly GLP-1 tablet for weight management and type 2 diabetes. In phase 1, with no human data.

02

How does GZC8072 work?

What it does in the body, and where.

Gan & Lee says GZC8072 is based on native GLP-1, made long-acting with its NovaPeptide platform and absorbable by mouth with its SupOraTide platform.

  1. 01
    GLP-1 receptor
    Like other GLP-1 drugs, it is meant to slow stomach emptying, blunt appetite and raise insulin after meals.
  2. 02
    Getting through the gut
    Peptides are mostly destroyed in the gut. Oral semaglutide uses the absorption enhancer SNAC and still absorbs only 0.4 to 1%. How SupOraTide works has not been disclosed.
  3. 03
    Weekly by mouth
    The company claims a longer half-life and much better oral bioavailability, without numbers. Its Chinese filing also calls the molecule 'biased' without saying what that means.
Receptors
HITSGLP-11

Acts on one receptor.

03

What else is it used for?

Each group 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.

Phase 1

Investigational
  • No dataSingle doses in healthy adults, then multiple doses for about 8 weeks in adults with overweight or obesity, against placebo. Weight, waist and glucose are secondary measures.
  • No dataThe release says 112 participants at several centres; the registry says 126 at one hospital.
  • No dataNo preclinical numbers (animal weight loss, half-life or bioavailability) have been published.
Often left out

Weight-loss figures circulating for Gan & Lee's GLP-1 drugs belong to bofanglutide (GZR18), a separate injection, not this tablet. The phase 1 size is 112 in the release and 126 on ClinicalTrials.gov, and the release calls it multicentre while the registry lists one site. It is a peptide, unlike orforglipron. 'Enhanced intrinsic GLP-1 receptor activity' is trade-press wording; the company says only 'enhanced intrinsic activity'.

The published record

Research index

0

Papers and trials about GZC8072

Europe PMC was searched on 13 October 2026 and returned nothing.

Counted from Europe PMC indexing, not read by a person.

GZC8072 vial rendering
Compound field notes

At a glance

Four things to know about GZC8072

01

Evidence

Investigational

02

Category

Weight loss and metabolic

03

Common vial

Varies

04

Half-life

Nothing published

04

How much, and do you cycle it?

The range, and whether you take breaks.

No dose disclosed, weekly (intended). No established pattern No range

No human schedule beyond the phase 1 has been published; the stated target is one tablet a week.

Compare this against the whole library →

05

How long does it stay in the body?

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

Nothing publishedNo figure

The company claims a prolonged half-life without numbers. The phase 1 will measure it.

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.

GZC8072 is not injected

It is taken by mouth (tablet). No doses have been disclosed in the registry or company releases. The company intends a once-weekly tablet. Any dose offered for it would be invented.

Cost per month
—
Cost per dose
—
Typical dose
—No range
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 GZC8072 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.
  • A personal or family history of medullary thyroid cancer or MEN 2, excluded from its trial as for every GLP-1 drug
  • Past pancreatitis, symptomatic gallbladder disease or high-risk gallstones
  • Reduced kidney function (eGFR below 90), excluded from the phase 1
  • Pregnancy or breastfeeding

Stop and get help

These are emergencies. Seek care.
  • Not applicable outside the trial. No product exists and no human side-effect profile has been published

Common effects

Expected, and usually mild.
  • No human data have been published
  • Immune responses against the drug are a primary endpoint of the phase 1

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

09

Is GZC8072 approved?

And where the numbers on this page come from.

No. GZC8072 is not approved anywhere and is currently in company-run clinical trials. There is no legal route to obtain it outside a trial.

What has happened recently

Not approved anywhere. China's NMPA approved trials for weight control in August 2026, and an approval for glucose control was reported in September 2026 (secondary sources only). The phase 1 (NCT07784699; China registry CTR20263271 by inference) started on 2 September 2026 at Beijing Shijitan Hospital: single doses in healthy adults, then multiple doses in adults with overweight or obesity, with 126 participants estimated on ClinicalTrials.gov against 112 in the company release. No US IND or designations were found.

Guides for this compound

Sources