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−28.7%Retatrutide Phase 2
11 TotalStack Compounds
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GLP-3 R 15mg

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GLP-3 R 15mg
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RetatrutideFat LossTriple-Agonist

GLP-3 R 15mg

Retatrutide

CAS: 2381609-35-2

Retatrutide (GLP-3 R) 15mg — the standard Clav stack supply. Triple GLP-1/GIP/Glucagon receptor agonist. Phase 2: −28.7% body weight at 48 weeks.

≥98% Purity
HPLC Verified
Research Grade
Lyophilized
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Orders $200+
$189.99 In Stock

For research purposes only. Not intended for human use.

Triple-Agonist: GLP-1R + GIPR + GcgR

Retatrutide activates three receptors simultaneously — the most receptor coverage of any GLP compound in research. GLP-1R drives hypothalamic appetite suppression and satiety. GIPR enhances insulin sensitivity and adipocyte lipid metabolism. GcgR activates hepatic beta-oxidation and brown adipose thermogenesis — an active fat-burning mechanism absent in semaglutide and tirzepatide. This third receptor is the differentiator that produced Phase 2 data of −28.7% at 48 weeks, the highest result ever recorded for a GLP compound.

Phase 2: −28.7% at 48 weeks

Retatrutide Phase 2 trial at 8mg/week produced −28.7% body weight reduction at 48 weeks. The trajectory had not plateaued at trial end, suggesting continued loss with extended protocols. This exceeds tirzepatide's best Phase 3 result (−20.9%) and semaglutide's best (−14.9%).

GcgR — The Third Mechanism

Glucagon receptor engagement drives hepatic fat oxidation and brown adipose thermogenesis. Unlike GLP-1/GIP which primarily suppress appetite, GcgR activation causes the body to burn fat directly — raising resting energy expenditure. This is the mechanism responsible for Retatrutide's clinical advantage.

Dose Escalation Protocol

Phase 2 used a 3-step escalation: 2mg/week (weeks 1-4) → 4mg/week (weeks 5-8) → 8mg/week (week 9+). The escalation minimizes GI side effects during adaptation. Running BPC-157 concurrently provides gut protection throughout.

Specifications

Chemical NameRetatrutide
CAS Number2381609-35-2
Vial Size15mg
FormLyophilized powder
Purity≥98% (HPLC verified)
Reconstitution5mL BAC water → 3mg/mL
Storage−20°C long-term / 4°C up to 6 weeks reconstituted

Research FAQ

Why does the Clav stack use Retatrutide over tirzepatide?

Retatrutide's triple-agonist profile (GLP-1 + GIP + Glucagon) produced −28.7% at 48 weeks vs tirzepatide's −20.9%. The glucagon receptor engagement drives hepatic fat oxidation and thermogenesis — mechanisms absent in dual agonists.

What is the reconstitution protocol for Retatrutide 15mg?

Add 5mL bacteriostatic water to the 15mg vial for a 3mg/mL concentration. Inject slowly along the vial wall — do not shake. Store reconstituted at 2-8°C for up to 6 weeks.

Should I run BPC-157 alongside Retatrutide?

Yes — BPC-157 is considered essential with any GLP protocol. Retatrutide delays gastric emptying and alters gut motility. BPC-157's gastroprotective mechanism (NO system upregulation) supports gut health throughout dose escalation.