Metabolic Research

Retatrutide5mg

$55

The lowest-concentration format of retatrutide, designed for fine-grained titration, dose-finding studies, or research protocols involving medication-sensitive subjects where smaller dose increments are required.

RetatrutideMetabolic Research

Overview

Retatrutide 5mg is the smallest-vial presentation of Eli Lilly's triple GLP-1/GIP/glucagon receptor agonist. The compound itself is identical across vial sizes — a 39-amino acid synthetic peptide with a C20 fatty diacid modification enabling albumin-mediated half-life extension and once-weekly subcutaneous dosing. What differs is the dose-finding precision the 5mg format enables.

Fine-grained titration is the core research use case for this vial size. The Phase 2 trial (NCT04881760) and Phase 3 TRIUMPH-4 (NCT05929066) both used 2mg / 4mg / 8mg / 12mg escalation schedules, with some Phase 3 arms adding a 6mg intermediate step to soften the GI side-effect ramp. The 5mg format supports research into even finer intermediate steps — 1mg microdose starts, 3mg transitional doses — which are relevant for subjects who exhibit exaggerated pharmacodynamic response to GLP-1 class drugs. It is also useful for late-phase dose-reduction research where subjects have reached maintenance and are being titrated down toward minimum effective doses.

All mechanistic data and clinical outcomes documented for the 8mg, 10mg, and 20mg formats apply here. Phase 3 TRIUMPH-4 reported 28.7% mean weight loss at 68 weeks, the strongest clinical weight reduction data in any obesity pharmacotherapy to date. The 5mg vial format is the most cost-efficient entry point for new research programs running conservative titration schedules where full 12mg exposure is not part of the protocol.

Mechanism of Action

Triple agonist at GLP-1R (appetite suppression), GIPR (insulin sensitization), and GCGR (hepatic lipolysis and energy expenditure); C20 fatty diacid modification enables once-weekly dosing via albumin binding.

Research Applications

Areas of peer-reviewed scientific inquiry where this compound has appeared.

  • Dose-finding and fine-grained titration research
  • Medication-sensitive responder studies
  • Obesity and adipose tissue research
  • Type 2 diabetes and insulin resistance
  • Non-alcoholic steatohepatitis (NASH)

Key Findings from the Literature

  1. 01Phase 3 TRIUMPH-4: 28.7% mean weight loss at 68 weeks across full dose range
  2. 02Supports 1mg microdose starter protocols for sensitive responders
  3. 03Identical pharmacology to 8mg, 10mg, and 20mg formats
  4. 04C20 fatty diacid modification enables once-weekly subcutaneous dosing

Certificates of Analysis1

Independent third-party lab reports for this peptide. Each CoA can be verified against its accession number at the testing lab.

1 independent test by Freedom Diagnostics Testing

TestResult
Purity (HPLC)99.952%
Identity (MS)Pass
Endotoxins (LAL)Pass

Lab: Freedom Diagnostics Testing

Accession: 2602120077 / 2602120078

Reports are verifiable against the issuing lab using the accession or batch identifier above.

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