Biohackr.Labs

CUT Protocol

Retatrutide R40 Maintenance Pen

Retatrutide maintenance — one pen, one month, your dose.

Key Attributes

  • One-month supply at your confirmed individual maintenance dose
  • Seamless transition from R25 or R50 onboarding — identical click precision
  • Avoids over-supplying volume beyond what your monthly protocol requires
  • Available on an ongoing basis through My Account in Bangkok and Thailand
  • Quality-controlled European-sourced Retatrutide — consistent batch to batch

Technical Specifications

Total Content
40 mg Retatrutide
CAS Number
2381609-22-7
Fill Volume
1.6 mL
Concentration
25 mg/mL
Per Click
0.25 mg/click
Total Clicks
160
Collection
CUT
Shipping
Cold-chain delivery · 2–8°C
฿12,000THB

Biohackr.Labs provides product education, protocol guidance, and private client support. Information on this website is not medical advice and does not replace consultation with a licensed healthcare professional.

Biohackr.Labs premium hard case open — precision pen and 10 individually sealed micro needles
Premium hard case open at angle — pen and needle kit in foam insert
Biohackr.Labs premium white hard case — closed with holographic logo

What's Included

Premium hard case.
Everything included.

Every Biohackr.Labs pen ships in our premium white hard case — holographic logo, foam-fitted interior. Inside: the precision pen, ten individually sealed 31G 8mm micro needles, and all documentation needed to begin your protocol correctly.

Precision pen

Pre-filled, batch quality-controlled pen system ready at your confirmed starting dose.

10× 31G micro needles

31G 8mm individually sealed sterile micro needles. Ten included as standard with every pen.

Protocol card

Starting dose, titration schedule, session guidance, and what to expect — specific to your protocol.

Batch QC documentation

Batch reference, preparation date, and compound specification. Not boilerplate — specific to your order.

Storage & handling guide

Temperature requirements, travel guidance, and handling notes with Bangkok climate context.

Private support access

WhatsApp, LINE, email, and My Account support throughout your protocol cycle.

Professional Packing

Strictly packed for
cold-chain delivery.

Peptide pen formulations are temperature-sensitive. Every order is packed as a refrigerated product and handled under strict cold-chain conditions — insulated temperature-control packaging with cold packs maintained at the standard refrigerated range of 2–8°C wherever available during transit.

Refrigerated cold-chain transport

Peptide pens are handled as refrigerated products throughout transit. Intended transport condition is controlled cold-chain delivery at 2–8°C wherever available. Available in supported cold-chain delivery areas only.

Temperature-control packaging

Insulated temperature-control packaging with cold packs engineered to maintain the product in the refrigerated range from preparation to handover — anywhere in Thailand with cold-chain delivery coverage.

Refrigerate immediately on receipt

Transfer to refrigerated storage the moment you receive your order. Do not leave unattended or delay collection. Tamper-evident sealing confirms product integrity at handover.

Biohackr.Labs temperature-controlled packaging — kraft shipping box open with insulated liner and sealed product inside
Biohackr.Labs temperature-controlled outer shipping box
Biohackr.Labs individually sealed product bag
Biohackr.Labs packaging components — thermal liner, insulated bag, sealed product
Biohackr.Labs product in premium sealed shipping bag

Step 01

Protocol Overview

Retatrutide maintenance — one pen, one month, your dose.

The R40 Maintenance Pen is designed for clients who have completed a structured Retatrutide onboarding protocol and confirmed their effective dose. Delivering 40 mg across 160 precision clicks, the R40 provides exactly one month of maintenance-phase support at the dose that works for you — without the larger volume of an onboarding pen. The rational next step after completing the R25 or R50.

Step 02

Mechanism of Action

In the maintenance phase of a Retatrutide protocol, the goal shifts from dose escalation to sustained metabolic equilibrium. The R40 delivers your confirmed effective dose consistently across a monthly cycle, supporting continued appetite regulation, metabolic rate maintenance, and body composition stability. The 0.25 mg per click precision remains identical to the onboarding pens, ensuring no dosing disruption at transition.

Suggested Use

One weekly subcutaneous administration at your confirmed maintenance dose. Dose confirmed through prior protocol and order review.

Who This Protocol Is For

For established Retatrutide users in Bangkok and Thailand who have completed onboarding and confirmed their effective dose. Not a starting protocol — requires prior onboarding and dose confirmation.

Storage — Bangkok & Thailand

Refrigerate between 2–8°C. Consistent storage is especially important for ongoing monthly protocols — establish a permanent refrigerated storage location before beginning maintenance phase.

Delivery — Thailand

Peptide pens are shipped under strict cold-chain handling — handled as refrigerated products at 2–8°C wherever available. Available in supported cold-chain delivery areas only.

Refrigerate immediately on receipt. You must be present to receive the delivery directly.

Potential Side Effects

  • GI effects — typically diminish once maintenance dose is established through onboarding; report any persistence through My Account
  • Injection site reactions — transient redness or discomfort at administration site
  • Dysesthesia (tingling or altered skin sensation) — reported at higher doses; relevant if dose increases from confirmed maintenance level
  • Cardiac effects under active investigation in ongoing Phase 3 trials — prior medical suitability review required

Order Review Required

All Biohackr.Labs orders are reviewed before confirmation. Dosing and administration are confirmed before fulfilment where required.

Enquire on WhatsAppAdd LINE

The Compound

What Is Retatrutide?

Retatrutide (LY3437943) is a synthetic once-weekly peptide developed by Eli Lilly — the first triple hormone receptor agonist to enter Phase 3 clinical trials. Where semaglutide activates one receptor and tirzepatide activates two, retatrutide simultaneously activates three: GLP-1, GIP, and glucagon. This triple mechanism produces compounding effects on appetite, fat metabolism, and energy expenditure that neither dual nor single agonists can replicate.

By targeting three complementary metabolic pathways at once, retatrutide addresses the biology of excess weight from multiple angles simultaneously. The result is weight loss outcomes that exceed what single or dual agonist compounds can achieve — including outcomes comparable to bariatric surgery in a subset of patients.

Semaglutide

Ozempic / Wegovy

1 receptor

Mechanism

GLP-1 only

Peak weight loss

~13.9%

Tirzepatide

Mounjaro / Zepbound

2 receptors

Mechanism

GLP-1 + GIP

Peak weight loss

~17.8–20.9%

Retatrutide

Pending (LY3437943)

3 receptors

Mechanism

GLP-1 + GIP + Glucagon

Peak weight loss

~28.3–30.3%

Cross-trial comparisons have inherent limitations. A head-to-head trial would be required for definitive conclusions.

Triple Mechanism

What Each Agonist Does

GLP-1

Glucagon-Like Peptide-1

Role

Appetite and insulin regulation

Slows gastric emptying to reduce caloric intake, suppresses appetite signals in the hypothalamus, and stimulates glucose-dependent insulin secretion. GLP-1 agonism is the foundation of semaglutide and tirzepatide — and the primary mechanism of all incretin-based compounds.

Key Effect

Appetite reduction + insulin sensitivity

Also in: Semaglutide, Tirzepatide

GIP

Glucose-dependent Insulinotropic Polypeptide

Role

Nutrient partitioning and fat cell metabolism

Enhances insulin sensitivity in peripheral tissues, modulates how the body partitions incoming calories between storage and use, and appears to amplify the appetite-suppressing effects of GLP-1 agonism. GIP is the second receptor targeted by tirzepatide — and a key contributor to its weight loss advantage over semaglutide.

Key Effect

Enhanced insulin sensitivity + fat cell regulation

Also in: Tirzepatide

Glucagon

Glucagon Receptor

Role

Energy expenditure and direct liver fat clearance

The critical differentiator. Glucagon receptor activation directly stimulates the liver to burn stored fat (fatty acid oxidation) and suppresses new fat synthesis (de novo lipogenesis). It also increases basal metabolic rate and thermogenesis — meaning the body burns more calories at rest. No approved obesity medication targets this receptor. It is the mechanism responsible for retatrutide's unprecedented liver fat reduction data.

Key Effect

Increased energy expenditure + hepatic fat clearance

Also in: Unique to Retatrutide among approved/late-stage compounds

Beyond Weight Loss

Emerging Benefits From Clinical Data

Clinical trial data surfacing across the TRIUMPH program suggests retatrutide may offer systemic benefits beyond weight management — driven by the glucagon receptor component that neither semaglutide nor tirzepatide possess.

Metabolic Liver Disease (MASLD/MASH)

The glucagon receptor component drives direct hepatic fat oxidation — the liver burns its stored triglycerides. Phase 2a data (Nature Medicine, 2024) showed 82.4% liver fat reduction and more than 85% liver fat normalization at the 12 mg dose. Phase 3 MASLD/MASH-specific trials are underway.

Knee Osteoarthritis

TRIUMPH-1 reported a nested knee osteoarthritis basket trial, with WOMAC pain scores reduced by up to 4.3 points (73.1%) at 80 weeks. TRIUMPH-4 remains the dedicated knee osteoarthritis study in the registry.

Systemic Inflammation

TRIUMPH-1 investigators noted "clear improvements in assessed cardiometabolic health measures" including inflammatory markers. The triple receptor mechanism appears to address metabolic inflammation through multiple pathways — weight-independent of the pure weight loss effect.

Insulin Resistance

TRIUMPH-2 topline data in adults with type 2 diabetes and obesity or overweight reported up to 20.8% mean weight loss and A1C reductions of up to 1.6 percentage points over 80 weeks.

Sleep Apnoea

TRIUMPH-1 reported a nested moderate-to-severe obstructive sleep apnoea basket trial, with apnea-hypopnea index reduced by up to 36.1 events per hour (60.6%) at 80 weeks.

Cardiovascular Outcomes

TRIUMPH-3 reported up to 22.6% mean weight loss at 80 weeks in adults with severe obesity and established cardiovascular disease. Its pre-specified cardiovascular event analyses were underpowered and inconclusive, so the dedicated TRIUMPH-Outcomes study remains the key cardiovascular and kidney outcomes trial.

All emerging benefit data is from Phase 2 or Phase 3 clinical trial publications and official Eli Lilly announcements. Retatrutide is investigational. Benefits described are not confirmed clinical indications.

Live Research

TRIUMPH Trial Tracker

Last updated

July 26, 2026

Eli Lilly TRIUMPH Phase 3 · published highlights + active registry watch

TRIUMPH-1Obesity and overweight (primary registrational trial)
Results PublishedJune 2026

28.3% avg weight loss at 80 weeks (12 mg). 30.3% at 104 weeks in the BMI >=35 extension. 45.3% lost >30% bodyweight.

TRIUMPH-2Obesity with type 2 diabetes
ActiveJuly 2026 topline readout

Topline Lilly readout: up to 20.8% mean weight loss at 80 weeks and A1C reductions up to 1.6 percentage points; detailed peer-reviewed results pending.

TRIUMPH-3Established cardiovascular disease
ActiveJuly 2026 topline readout

Topline Lilly readout: up to 22.6% mean weight loss at 80 weeks; cardiovascular event analyses were inconclusive because event rates were lower than expected.

TRIUMPH-4Obesity with knee osteoarthritis
Results PublishedDec 2025

28.7% avg weight loss at 68 weeks (12 mg). Substantial knee pain reduction.

TRIUMPH-OutcomesCardiovascular and kidney outcomes
ActiveRegistry updated Jul 2026

Large event-driven Phase 3 outcomes study; ClinicalTrials.gov lists estimated completion in 2029.

Lilly plans to submit a Biologics License Application for U.S. approval in Q1 2027. · ClinicalTrials.gov API checked July 26, 2026. Review monthly, and immediately after Lilly readouts or registry updates. Data is reviewed against official registries, Eli Lilly releases, and peer-reviewed publications. Retatrutide is investigational and not approved for clinical use.

Key Statistics

Phase 3 TRIUMPH Data Highlights

30.3%

Average weight loss at 104 weeks

12 mg dose, TRIUMPH-1 — comparable to bariatric surgery outcomes

Eli Lilly, June 2026

45.3%

Patients losing >30% body weight

12 mg dose — a threshold historically achievable only through surgery

TRIUMPH-1, June 2026

70.3 lbs

Average weight lost at 80 weeks

12 mg dose, TRIUMPH-1 — highest weight loss for any non-surgical intervention in Phase 3

Eli Lilly, June 2026

82.4%

Liver fat reduction at 48 weeks

12 mg dose, Phase 2a liver sub-study — unprecedented for any pharmacological compound

Nature Medicine, 2024

>85%

Patients achieving normal liver fat levels

<5% liver fat at the 12 mg dose after 24 and 48 weeks

Nature Medicine, 2024

5,800+

Participants enrolled in TRIUMPH program

Across four global registrational trials — the largest retatrutide trial program to date

Eli Lilly, 2026

My Account

Premium imported peptide pens in Bangkok.

Reviewed My Account ordering · European-sourced · Quality-controlled · Thailand delivery

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