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Collection / GLP-3 40mg Pen

PEPTIVIAGLP-3 40mg Pen40 mgRESEARCH USE ONLY
Metabolic research · pen

GLP-3 40mg Pen

GLP-3 is the catalogue name for retatrutide, a GIP, GLP-1 and glucagon receptor triple agonist. Controlled clinical research examines metabolic and body-weight endpoints for the investigational molecule.

$599.99 CAD

Simulation only · No real order or payment.

BrandPEPTIVIA
Format / strengthpen · 40 mg
Pack quantity1
GLP-3 is the catalogue alias for retatrutide. Form and exact strength remain distinct identifiers.

GIP, GLP-1 and glucagon receptor triple agonist

Also known as: Retatrutide · LY3437943

Human trial
Research & handling

Not for human or veterinary use. Storage, handling, identity and purity require verified batch documentation. No dosing or treatment advice is provided.

RESEARCH FOCUS

At a glance

Three receptor targets

GIP, GLP-1 and glucagon receptor activity frame its metabolic research identity.

Metabolic-health research

Reviewed trials investigate body-weight endpoints in defined populations.

Clinical evidence

Trial interventions and monitored participants are distinct from a catalogue vial or pen.

Explore the study context and sources below. For laboratory research only.

EXPLORE THE EVIDENCE

Studies & context

GLP-3 is a nickname for retatrutide, studied in adults for metabolic and body-weight outcomes. It targets GLP-1, GIP and glucagon receptors: three targets, not three established benefits.

Human trial
Human trial

Jastreboff et al. (NEJM, 2023) randomized 338 adults with obesity, or overweight plus a weight-related condition, in a 48-week phase 2 trial.

Study limitations

Receptor activity concerns metabolic signalling; measured weight change is a separate endpoint, not proof of an appetite mechanism or a PEPTIVIA product effect.

Jastreboff et al., 2023 ↗
Human trial

At week 48, least-squares mean body-weight change was −24.2% in the investigational 12 mg arm (starting at 2 mg), versus −2.1% with placebo; week 24 was the primary endpoint.

Study limitations

This is a specific trial arm and secondary endpoint, not expected weight loss from a purchased vial or a use recommendation.

Jastreboff et al., 2023 ↗
Human trial

Gastrointestinal adverse events were dose-related and mostly mild to moderate; heart-rate increases peaked at week 24 and declined thereafter.

Study limitations

Safety findings belong to the studied investigational molecule and monitored trial conditions, not PEPTIVIA’s batch.

Jastreboff et al., 2023 ↗

Published research is separate from PEPTIVIA identity, content, purity, sterility and batch documentation. No source-supplier report verifies PEPTIVIA material.