NZ Retatrutide Research
TRIUMPH-4 topline: 28.7% average weight loss at 68 weeks /// Triple agonist: GIP · GLP-1 · GCGR receptor activation /// New Zealand · Independent Research Resource /// TRIUMPH-4 reported · additional Phase 3 readouts expected in 2026 /// TRIUMPH-4 topline: 28.7% average weight loss at 68 weeks /// Triple agonist: GIP · GLP-1 · GCGR receptor activation /// New Zealand · Independent Research Resource ///
New Zealand’s Retatrutide Research Hub

The Next
Generation
Triple Agonist

Retatrutide simultaneously activates three metabolic receptors — GIP, GLP-1, and glucagon. In our full Retatrutide New Zealand guide, we break down how this triple agonist works, how it compares to existing GLP-1 drugs, and what current clinical data means for metabolic research in Aotearoa.

28.7%
Mean Weight Loss
Receptor Targets
Ph.3
Trial Stage
Phase 3 Topline

TRIUMPH-4: 28.7% Mean Weight Loss at 68 Weeks

Breaking down Lilly’s first successful Phase 3 readout in obesity with knee osteoarthritis — the numbers, the caveats, and what it means.

8 min read
Mechanism

Triple Receptor Agonism: Why the GCGR Target Changes Everything

How glucagon receptor activation sets retatrutide apart from existing GLP-1 therapies.

6 min read
NZ Access

Research-Use Peptides in New Zealand: A Practical Overview

Regulatory landscape, clinical context, and what New Zealand researchers need to understand.

5 min read
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Three Targets.
One Molecule.

Where semaglutide and tirzepatide act on one or two receptors, retatrutide (LY3437943) is a once-weekly injectable peptide that simultaneously activates the GIP, GLP-1, and glucagon receptors — the first of its kind to reach late-stage clinical development.

The additional glucagon receptor component may drive significantly greater energy expenditure and fat oxidation compared to GLP-1 monotherapy, which researchers believe may explain the higher weight-loss figures seen in trials.

For a deeper comparison, see our retatrutide vs semaglutide comparison and our retatrutide vs tirzepatide analysis.

Research Context
Retatrutide is being studied as a next-generation triple agonist targeting GIP, GLP-1, and glucagon receptors.
  • GLPreceptor
    GLP-1 Receptor Agonism
    Reduces appetite and food intake. Slows gastric emptying. Shared mechanism with semaglutide and tirzepatide. Learn more in our GLP-1 mechanism guide.
  • GIPreceptor
    GIP Receptor Agonism
    Enhances insulin secretion and may influence GLP-1 receptor sensitivity. Also active in tirzepatide.
  • GCGreceptor
    Glucagon Receptor Agonism
    The third target — associated with increased energy expenditure, hepatic fat changes, and retatrutide’s distinct research profile.

Latest Research
& Analysis

All Guides
TRIUMPH-4 Key Data

The numbers
behind the latest TRIUMPH headline

28.7%
Mean body weight reduction at 68 weeks in the 12 mg retatrutide arm
Lilly TRIUMPH-4 topline
445
Participants randomized in the Phase 3 TRIUMPH-4 trial
NCT05931367
68wk
Co-primary endpoint timepoint used in the first successful Phase 3 readout
TRIUMPH-4 protocol
Receptor targets: GIP · GLP-1 · Glucagon. First triple agonist in Phase 3
LY3437943 · Eli Lilly

This page includes TRIUMPH-4 topline Phase 3 context alongside earlier published Phase 2 research. This site presents research information only. Individual outcomes vary. Not medical advice.

Retatrutide research, comparisons, and GLP-1 science.

Start with the complete Retatrutide New Zealand guide, then explore how retatrutide compares with established metabolic research compounds including semaglutide and tirzepatide.

For a deeper mechanism breakdown, read our GLP-1 mechanism of action guide. You can also browse the full retatrutide guides library. For researchers looking into availability, see our where to buy retatrutide NZ guide, which covers supplier transparency, COA checks, and research-use sourcing red flags.