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Developer: Eli Lilly and Company Classification: Triple Agonist (GIP/GLP-1/Glucagon receptors) Administration: Once-weekly subcutaneous injection Development Status: Phase 3 clinical trials Expected FDA Approval: Q3 2026 to Q1 2027 Developer: Boehringer Ingelheim Classification: Dual Agonist (Glucagon/GLP-1 receptors) Administration: Once-weekly subcutaneous injection Development Status: Phase 3 clinical trials (SYNCHRONIZE program) Regulatory Status: FDA Breakthrough Therapy designation for MASH Retatrutide emerged from Eli Lillys research into multi-receptor agonism

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This collaborative approach between you, your prescribing clinician, and nutrition professionals ensures that calorie intake supports both your treatment goals and overall health, maximising the benefits of GLP-1 therapy whilst minimising potential risks

readers should verify current details directly with altRx and, for regulatory questions, consult FDA.gov

When you choose Primary Care Center of Clear Lake for your weight loss journey, your care begins with a comprehensive assessment by one of our experienced providers