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ALLUVI · Triple agonist
Next-generation triple agonist · 40 mg pen · ALLUVI Healthcare
40 mgShips tomorrow (Mon) · before 19:00
Delivery Tue, Sep 29 · Nova Poshta
💊 Try for 8 000 ₴/mo
Starting dose 2.5 mg · no pen needed · save 20%
Retatrutide 40 mg by ALLUVI Healthcare — injection pen with triple agonist GLP-1/GIP/glucagon. 4 full doses of 10 mg (40 mg total), 12 needles included, dosing instructions.
In short: Retatrutide 40 mg (ALLUVI)
Price: 18 000 ₴. In stock. Delivery across Ukraine — Nova Poshta, 1–3 days; Kyiv — courier, 1–2 hours. Cold chain 2–8°C. 24/7 specialist support included in the price. Order on the official DOZA website: doza.clinic.
Specialist support included in the price
A personal DOZA specialist guides you throughout the entire course — from first consultation to results.
Triple agonist — next generation
Retatrutide — a triple GLP-1/GIP/glucagon agonist. Investigational Phase 3 molecule by Eli Lilly. Not approved by FDA/EMA.
Manufacturer: ALLUVI
ALLUVI — a brand of peptide products for metabolic correction programs. Manufacturing meets GMP standards.
Free consultation
Benefits
- ✓Triple mechanism of action — only GLP-1 + GIP + glucagon agonist
- ✓40 mg in pen — 4 full doses of 10 mg (up to 16 weeks with gradual escalation)
- ✓12 needles included + ALLUVI dosing instructions
- ✓Isotonic solution, pH 6.5–7.5 — comfortable injection
- ✓Up to 28.3% weight loss over 80 weeks on the 12 mg/week dose (Phase 3 TRIUMPH-1, topline 2026); Phase 2: up to 24% over 48 weeks (NEJM 2023)
- ✓Cold chain delivery with cooling elements (2–8°C) across Ukraine
- ✓Free 24/7 DOZA specialist support throughout the entire course
Retatrutide 40 mg (ALLUVI) — detailed description
Retatrutide by ALLUVI Healthcare — the world's first triple agonist targeting GLP-1, GIP and glucagon receptors in a convenient injection pen.
Each full dose contains 10 mg of retatrutide, with a total of 40 mg active ingredient in the pen. The pen allows dosing from 2.5 mg to 10 mg using the dial mechanism.
Dosing schedule per ALLUVI instructions:
• Weeks 1–4 (starting dose): 2.5 mg once weekly
• Weeks 5–8: 5 mg once weekly
• Weeks 9–13: 7.5 mg once weekly
• Weeks 14+: 10 mg once weekly
Do not increase dose until hunger sensation returns. Important to maintain balanced nutrition throughout the course.
Important: 40 mg is the total pen content of the active substance, not the weekly dose. In Phase 3 TRIUMPH, weekly doses ranged 2–12 mg (2 mg start, escalation every 4 weeks to target doses of 4/9/12 mg); the −28.3% result at 80 weeks (TRIUMPH-1, topline 2026) was achieved on the 12 mg/week dose.
Retatrutide (LY3437943) is an investigational molecule developed by Eli Lilly. This ALLUVI product is manufactured by a third party and is not manufactured, supplied or approved by Eli Lilly.
How it works — mechanism of action
Retatrutide is the only triple agonist GLP-1 + GIP + glucagon. Acts on three receptors simultaneously:
1. GLP-1 — reduces appetite, slows gastric emptying, regulates glucose levels.
2. GIP — enhances GLP-1 effects and improves fat tissue metabolism.
3. Glucagon — activates lipolysis (fat breakdown) and thermogenesis (calorie burning).
In Phase 3 TRIUMPH-1 (topline 2026), participants on 12 mg lost an average of 28.3% body weight over 80 weeks (efficacy estimand) — the highest published result in the GLP-1 class. Phase 2 (NEJM 2023): up to 24% over 48 weeks.
Dosage
Starting dose: 2.5 mg once weekly (weeks 1–4)
Weeks 5–8: 5 mg once weekly
Weeks 9–13: 7.5 mg once weekly
Weeks 14+: 10 mg (full dose) once weekly
Subcutaneous injection in abdomen, thigh or shoulder area. Same day each week. Do not increase dose until hunger sensation returns.
What's in the kit
Шприц-ручка ALLUVI Retatrutide з набірним механізмом дозування.
• 1 ручка = 40 мг ретатрутиду (4 повні дози по 10 мг)
• 12 одноразових голок ALLUVI в комплекті
• Інструкція з покроковим дозуванням (Dosage Guide)
• Набірний механізм: від 0 до 10 мг за один оберт
Composition
Діюча речовина: ретатрутид (retatrutide) 10 мг на дозу, 40 мг загалом у ручці.
Допоміжні речовини: натрію хлорид, натрію цитрат, лимонна кислота моногідрат, полісорбат 80, бактеріостатична вода.
Для корекції pH використано хлористоводневу кислоту та/або натрію гідроксид.
Розчин ізотонічний, pH 6.5–7.5.
Storage
Зберігати в холодильнику при температурі 2–8°C. Не заморожувати.
Зберігати ручку в картонній упаковці для захисту від світла.
Після першого використання — утилізувати через 12 тижнів.
Не зберігати з приєднаною голкою.
Тільки для підшкірного введення.
Клінічні дослідження
Retatrutide (LY3437943 40 mg) — потрійний агоніст GLP-1 + GIP + глюкагон Eli Lilly. Phase 3 TRIUMPH-1/2/3: topline 2026, до −28.3% ваги за 80 тижнів (12 мг). Подача BLA у FDA — план Q1 2027. На /research зібрана доказова база Phase 2/3 та статус trials.
- TRIUMPH-1 Phase 3 topline: -28.3% at 80 weeks (12 mg), -30.3% at 104 weeks (Lilly, May 2026)ClinicalTrials.gov · 2026
- Triple-Hormone-Receptor Agonist Retatrutide for Obesity — Phase 2 Trial (NEJM 2023)PubMed · 2023
Retatrutide is an investigational drug. Phase 3 TRIUMPH-1/2/3 topline results reported in 2026; US BLA planned Q1 2027. Not approved by FDA, EMA or МОЗ України as of August 2026.
View full клінічні дослідження database →Titration protocol to 40 mg (retatrutide (triple GLP-1 / GIP / glucagon agonist))
Starting dose for all Phase 3 TRIUMPH participants
First escalation (target dose for the 4 mg group)
Intermediate escalation step
Target dose for the 9 mg group
Maximum TRIUMPH-1 target dose (−28.3% at 80 weeks)
Injection once weekly (per study protocol), subcutaneous (abdomen, thigh or upper arm). Expected weight loss at the 12 mg/week dose: -28.3% over 80 weeks (Phase 3 TRIUMPH-1, topline 2026) (based on clinical studies).
Who is Retatrutide 40 mg for
- Retatrutide is an investigational drug (Phase 3), not yet approved by the FDA/EMA
- Triple GLP-1 / GIP / glucagon agonist — a unique mechanism of action
- For patients for whom single (Ozempic) or dual (Mounjaro) agonists did not deliver enough effect
- Strictly under medical supervision
Retatrutide 40 mg — compared to other doses
- Retatrutide 12 mg showed -28.3% weight loss over 80 weeks in Phase 3 TRIUMPH-1 (topline 2026, efficacy estimand); Phase 2 (NEJM 2023): ~24% over 48 weeks
- In separate trials the numeric result is higher than Mounjaro 15 mg (-22.5%, SURMOUNT-1), but a direct head-to-head trial (NCT06662383) is still ongoing — clinical superiority has not been established
- Key difference: retatrutide activates the glucagon receptor, increasing energy expenditure
- Phase 3 results are topline/press-release level — full peer-reviewed publications pending; BLA (US) planned Q1 2027
FAQ about Retatrutide 40 mg (ALLUVI)
1 ALLUVI Retatrutide injection pen (40 mg total, dial mechanism up to 10 mg per dose), 12 single-use ALLUVI needles and dosing instructions (Dosage Guide) with step-by-step schedule from 2.5 mg to 10 mg.
Valentyna Tytorenko
Diploma-certified endocrinologist, certified dietitian and nutritionist
Other Retatrutide dosages
DOZA client reviews for Retatrutide 40 mg (ALLUVI)
Retatrutide 40 mg (ALLUVI) — noticeable results in just 3 weeks. Cold chain delivery, everything neat. Thank you, DOZA!
Ordering Retatrutide 40 mg (ALLUVI) via DOZA — fast delivery across Ukraine. Consultant helped choose the right dose. Triple agonist works more effectively.
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Before/after photos · numbers · timelines · reviews
Other Retatrutide dosages
Buy Retatrutide 40 mg in Ukraine
Buy Retatrutide 40 mg (ALLUVI) — next-generation triple GLP-1/GIP/glucagon agonist from DOZA. Next-generation triple agonist · 40 mg pen · ALLUVI Healthcare. Dosage 40 mg — for optimal therapeutic effect. Order via DOZA online service, delivery 1–2 days.
Retatrutide 40 mg (ALLUVI) price — 18 000 ₴.Cold chain delivery in thermal box.
Free DOZA specialist consultation. Available 24/7.
Buy Retatrutide 40 mg (ALLUVI) in Ukraine — DOZA online service with delivery in 1–2 days. Specialist consultation included.
⚠️ Retatrutide is an investigational product currently undergoing Phase 3 clinical trials. Results may vary. Consult a specialist before starting the program. Retatrutide is currently undergoing large-scale Phase 3 clinical trials (the TRIUMPH program). Final regulatory approval is expected after the completion of trials.
