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Approved In China 2026

Ecnoglutide

Also known as XW003

Summary coverage

At a glance

What it is
cAMP-biased GLP-1 agonist approved in China, appearing in gray-market channels.
Evidence
Clinical trialsHow the tiers workThe BMJ network meta-analysis groups ecnoglutide with mazdutide and retatrutide in a 13.1–14.6% weight-loss band, at very low to low certainty, meaning the effect estimate could move substantially with further evidence. Why this tier
Half-life
About 5 to 6 days
From Guo et al., Molecular Metabolism, 2023
Routes
Subcutaneous
Category
Metabolic
FDA
Investigational
As of 3 August 2026. What that means
WADA
We do not state a status

Putting Ecnoglutide on a schedule, with the vial it comes from and a log of each dose, happens in the app: Claritide for iPhone.

Evidence

Why this tier

The BMJ network meta-analysis groups ecnoglutide with mazdutide and retatrutide in a 13.1–14.6% weight-loss band, at very low to low certainty, meaning the effect estimate could move substantially with further evidence. It is also in study for adolescents, for obesity with obstructive sleep apnoea, and for obesity with knee osteoarthritis. There is no US label.

Overview

What it is

Ecnoglutide is a cAMP-biased GLP-1 receptor agonist from Sciwind Biosciences, given once weekly by subcutaneous injection with an oral tablet in development. China approved it in January 2026 for glycaemic control in type 2 diabetes and in March 2026 for long-term weight management. It is not FDA-approved and has no US label.

Mechanism

How it works

Ecnoglutide is described as cAMP-biased: it preferentially engages the cAMP signalling arm downstream of the GLP-1 receptor rather than the beta-arrestin arm. The claimed advantage of biased agonism is less receptor internalisation and therefore more sustained signalling. The clinical relevance of that bias, as against the ordinary GLP-1 effects of appetite suppression, delayed gastric emptying and glucose-dependent insulin release, is not something the published outcome data separates out.

Dosing

Commonly researched ranges

These are figures reported in published literature and practitioner protocols: a commonly researched range, not a recommendation. Claritide does not tell you what to take.
  • Obesity Phase 3 arms (SLIMMER)1.2–2.4 mg

    Once weekly for 48 weeks

    Three arms and nothing between them: 1.2, 1.8 and 2.4 mg weekly. 1.2 and 1.8 are the published figures and are not rounded here. This is the ladder behind the March 2026 Chinese approval for weight management.

  • Type 2 diabetes escalation (EECOH-1)0.3–1.2 mg

    Once weekly, escalated 0.3 → 0.6 → 1.2 mg

    A different indication and a different ladder. Kept separate on purpose: the diabetes escalation tops out where the obesity ladder starts.

Cycle guidance
Not established in available literature
Goals
Fat loss
Legal standing

Where this sits with the FDA

Dated, sourced, and separate from whether it works. Removal from a warning list is not permission to compound.
Investigationalas of 3 August 2026 · US

Approved in China and not FDA-approved, with no US label. Material reaching the US through international gray-market channels has no US regulatory oversight of any kind.

Last change · 1 March 2026 · China approved ecnoglutide for long-term weight management in March 2026, following approval for type 2 diabetes in January 2026; our sources do not give exact days.

Primary source
Sport

WADA status

The 2026 Prohibited List entered force on 1 January 2026.
We do not state a status

Not named on the 2026 Prohibited List. We could not determine a classification and do not state one.

We looked and could not resolve it. This is not the same as "not prohibited". Treat it as unresolved and check with your federation before competing.

Reconstitution

Mixing recipes our sources document

Concentration (mg/mL) = vial mg ÷ diluent mL. On a U-100 barrel, 1 unit = 0.01 mL.

Not established in available literature. Use the calculator with the figures printed on your own vial.
Open the calculator

Expectations

Week by week

What our material describes people reporting. Individual responses vary widely.

Not established in available literature.

Tolerability

Side effects

Grouped by how often our sources report them. Percentages appear only where a published trial figure exists.

Not established in available literature. Absence from this page does not mean absence of risk. It means our sources publish no side-effect profile for Ecnoglutide.

Safety

Contraindications and interactions

Do not use if

Not established in available literature.

Interactions

Not established in available literature.

Absence from this list does NOT mean safety. It means lack of research.

Handling

Storage and cost

Storage
Our sources publish no reconstitution or storage protocol for ecnoglutide.
Cost
Not established in available literature
Deep dive

Ecnoglutide in full

Limited coverage

Ecnoglutide (XW003) is a cAMP-biased GLP-1 receptor agonist from Sciwind Biosciences. Once weekly, subcutaneous, with an oral tablet in development.

Approved in China in January 2026 for glycaemic control in type 2 diabetes, and in March 2026 for long-term weight management in adults with obesity, or overweight plus at least one comorbidity. Not FDA-approved, no US label.

Where it sits

The BMJ network meta-analysis of the whole weight-loss class groups ecnoglutide with mazdutide and retatrutide in a 13.1 to 14.6% weight-loss band, at very low to low certainty.

That certainty rating is the part worth reading. It means the estimate rests on limited or indirect evidence and could move substantially as more data arrives. A number in the same band as a better-evidenced drug is not the same claim as a number with the same confidence behind it.

Further studies are running in adolescents, in obesity with obstructive sleep apnoea, and in obesity with knee osteoarthritis.

It is here because approval in one large market is how compounds start appearing in international gray-market channels, and because a US buyer sourcing it that way gets neither the Chinese regulatory oversight nor the American kind.

References

Sources

  1. 1
    BMJ network meta-analysis of weight-loss agents, 2026
  2. 2
    Lancet Diabetes & Endocrinology · SLIMMER Phase 3, the 1.2 / 1.8 / 2.4 mg weekly obesity arms (dose review, 2026-08-17)
  3. 3
    EECOH-1 · the type 2 diabetes escalation, 0.3 → 0.6 → 1.2 mg weekly (dose review, 2026-08-17)
  4. 4
    Sciwind Biosciences · NMPA approval for chronic weight management, 6 March 2026 (dose review, 2026-08-17)

Every record in this library is free to read, and it stays free. Your own schedule, vials and log live in the app: Claritide for iPhone.