Results & Expectations
    Retatrutide

    Retatrutide Weight Loss by Starting BMI

    Your starting BMI influences both the absolute pounds you lose and the health impact of that weight loss. Here is what Phase 2 data tells us about retatrutide outcomes across different BMI categories.

    Published: April 3, 202613 min read

    Patients come to retatrutide from different starting points -- BMI 28 with prediabetes, BMI 38 with type 2 diabetes, BMI 48 with multiple comorbidities. Phase 2 data (Jastreboff et al., NEJM 2023) showed that retatrutide produced significant weight loss across the BMI spectrum, but the absolute pounds lost and the clinical impact of that loss vary by where you start. Understanding these differences helps set realistic, personalized expectations.

    Data Limitations

    BMI-stratified results from Phase 2 are limited by small subgroup sizes. Phase 3 will provide more detailed analysis by starting BMI. Retatrutide is investigational.

    Percentage vs Absolute Weight Loss

    A crucial distinction: percentage weight loss tends to be relatively consistent across BMI categories (20-24% at the highest dose), but absolute weight loss in pounds varies dramatically. A 200-pound patient losing 24% loses 48 pounds. A 350-pound patient losing 24% loses 84 pounds. The percentage is the same; the practical impact differs.

    Outcomes by BMI Category

    For patients with BMI 27-30 (overweight): expected loss of approximately 15-20% body weight (30-45 pounds). This group may achieve normal BMI range. Health improvements include resolution of prediabetes, blood pressure normalization, and reduced joint stress. For patients with BMI 30-35 (class I obesity): expected loss of approximately 20-24% body weight (45-65 pounds). Many achieve overweight or normal BMI range. Diabetes risk drops dramatically. For patients with BMI 35-40 (class II obesity): expected loss of approximately 20-24% body weight (55-80 pounds). Most move to class I obesity or overweight category. Major improvements in mobility, sleep, and metabolic health. For patients with BMI 40+ (class III obesity): expected loss of approximately 20-24% body weight (70-100+ pounds). Significant BMI reduction but may remain in obesity category. Dramatic improvements in quality of life and comorbidity burden despite remaining elevated BMI.

    The Health Impact Varies by Starting BMI

    Interestingly, patients with lower starting BMIs may see the most dramatic health improvements relative to weight lost. Moving from BMI 33 to 25 crosses the threshold from obesity to normal weight, resolving many weight-related conditions entirely. Moving from BMI 48 to 37 provides enormous health benefit but still leaves the patient in the obesity category with ongoing health risks. This does not diminish the value of treatment for higher BMI patients -- the absolute health improvement from losing 80+ pounds is massive -- but it helps set appropriate expectations for what the final result looks like.

    To start your weight loss journey, visit our treatments page.

    Medical Disclaimer

    This article is for educational purposes only. Retatrutide is not FDA-approved. Results from Phase 2 data (Jastreboff et al., NEJM 2023). Individual results vary. Consult a healthcare provider.

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    Sources & References

    1. Wilding JPH et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. NEJM 2021;384:989-1002.
    2. Jastreboff AM et al. Tirzepatide Once Weekly for the Treatment of Obesity. NEJM 2022;387:205-216.
    3. Lincoff AM et al. Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes. NEJM 2023;389:2221-2232.
    4. FDA Prescribing Information for Wegovy (semaglutide) and Zepbound (tirzepatide).

    What does the published clinical evidence show for retatrutide?

    Peer-reviewed evidence: Retatrutide 12 mg produced a mean body weight reduction of approximately 24.2% at 48 weeks in adults with obesity in a Phase 2 trial, the highest published mean weight reduction for any GLP-1-class agent in obesity to date. (Source: Jastreboff et al. Phase 2 trial, NEJM 2023). Trimi is preparing for launch; compounded availability depends on FDA-cleared compounding pathways. Results vary by individual; eligibility is determined by a licensed clinician.

    Retatrutide 12 mg produced a mean body weight reduction of approximately 24.2% at 48 weeks in adults with obesity in a Phase 2 trial, the highest published mean weight reduction for any GLP-1-class agent in obesity to date., Jastreboff et al. Phase 2 trial, NEJM 2023
    Retatrutide 12 mg reduced HbA1c by approximately 2.02 percentage points at 36 weeks in patients with type 2 diabetes, compared with 1.41 points on dulaglutide 1.5 mg., Rosenstock et al. Phase 2 T2D trial, Lancet 2023

    Key Takeaways

    • Retatrutide 12 mg produced a mean body weight reduction of approximately 24.2% at 48 weeks in adults with obesity in a Phase 2 trial, the highest published mean weight reduction for any GLP-1-class agent in obesity to date. (Source: Jastreboff et al. Phase 2 trial, NEJM 2023)
    • Retatrutide 12 mg reduced HbA1c by approximately 2.02 percentage points at 36 weeks in patients with type 2 diabetes, compared with 1.41 points on dulaglutide 1.5 mg. (Source: Rosenstock et al. Phase 2 T2D trial, Lancet 2023)
    • Retatrutide is investigational and not FDA-approved as of publication. Trial findings reported here are from Phase 2 / Phase 3 studies in peer-reviewed sources cited below.
    • Eligibility requires evaluation by a licensed clinician: BMI ≥30, or BMI ≥27 with at least one weight-related comorbidity (type 2 diabetes, hypertension, dyslipidemia, obstructive sleep apnea, cardiovascular disease). Contraindications include personal or family history of medullary thyroid carcinoma, MEN 2 syndrome, pancreatitis, severe gastrointestinal disease, severe renal impairment, pregnancy, and breastfeeding.
    • Common GLP-1 receptor agonist adverse effects include nausea, vomiting, diarrhea, constipation, and gallbladder events. Dose titration over weeks improves tolerability. Severe gastrointestinal symptoms may cause dehydration and increase acute kidney injury risk.
    • This is general information based on the cited evidence, not medical advice. Treatment decisions require evaluation by a licensed clinician familiar with your individual medical history, BMI, and comorbidities.

    Medically Reviewed

    TMRT

    Trimi Medical Review Team

    Clinical review workflow for GLP-1 safety, dosing, and access content

    Team-based medical review process documented in Trimi's Medical Review Policy

    Last reviewed: February 7, 2026

    TCCT

    Written by Trimi Clinical Content Team

    Medical Writers & Healthcare Professionals

    Our clinical content team includes registered nurses, pharmacists, and medical writers who specialize in translating complex medical information into clear, actionable guidance for patients.

    Medically reviewed by Trimi Medical Review Team, Clinical review workflow for GLP-1 safety, dosing, and access content

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    Scientific References

    1. Jastreboff AM, Kaplan LM, Frías JP, et al. (2023). Triple-Hormone-Receptor Agonist Retatrutide for Obesity, A Phase 2 Trial. New England Journal of Medicine.Read StudyDOI: 10.1056/NEJMoa2301972
    2. Rosenstock J, Frias J, Jastreboff AM, et al. (2023). Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial. The Lancet.Read StudyDOI: 10.1016/S0140-6736(23)01053-X
    3. ClinicalTrials.gov (2024). A Study of Retatrutide (LY3437943) in Participants Who Have Obesity or Are Overweight (TRIUMPH-1), NCT05929066. ClinicalTrials.gov.Read Study
    4. Garvey WT, Mechanick JI, Brett EM, et al. (2024). American Association of Clinical Endocrinology / American College of Endocrinology Comprehensive Clinical Practice Guidelines for Medical Care of Patients with Obesity. Endocrine Practice.Read StudyDOI: 10.4158/EP161365.GL
    5. American Heart Association (2021). Obesity and Cardiovascular Disease: A Scientific Statement From the American Heart Association. Circulation.Read StudyDOI: 10.1161/CIR.0000000000000973
    6. Apovian CM, Aronne LJ, Bessesen DH, et al. (2015). Pharmacological Management of Obesity: An Endocrine Society Clinical Practice Guideline. Journal of Clinical Endocrinology & Metabolism.Read StudyDOI: 10.1210/jc.2014-3415

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