What are the available doses of Retatrutide (generic name) for patients with obesity or type 2 diabetes?

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Retatrutide Available Doses

Retatrutide is available in 1 mg, 4 mg, 8 mg, and 12 mg doses, administered as once-weekly subcutaneous injections. 1, 2, 3

Dosing Information from Clinical Trials

Available Dose Strengths

  • 1 mg weekly 1, 3
  • 4 mg weekly (with initial dose escalation starting at 2 mg or 4 mg) 1, 2, 3
  • 8 mg weekly (with initial dose escalation starting at 2 mg or 4 mg) 1, 2, 3
  • 12 mg weekly (with initial dose escalation starting at 2 mg) 1, 2, 3

Dose Escalation Strategies Studied

Multiple starting dose approaches have been evaluated in clinical trials to minimize gastrointestinal side effects: 2, 3

  • Lower starting doses (2 mg) followed by escalation were associated with better tolerability compared to starting at 4 mg directly 3
  • Dose-dependent increases in efficacy were observed across the range from 1 mg to 12 mg 1, 4, 3

Efficacy by Dose

Weight Loss Outcomes at 24 Weeks

  • 1 mg: -7.2% body weight reduction 1, 3
  • 4 mg: -12.9% body weight reduction 3
  • 8 mg: -17.3% body weight reduction 3
  • 12 mg: -17.5% body weight reduction 1, 3

Weight Loss Outcomes at 48 Weeks

  • 1 mg: -8.7% body weight reduction 3
  • 4 mg: -17.1% body weight reduction 3
  • 8 mg: -22.8% body weight reduction 3
  • 12 mg: -24.2% body weight reduction 3

Glycemic Control in Type 2 Diabetes (24 Weeks)

  • 4 mg: HbA1c reduction of -1.39% 2
  • 8 mg (slow escalation): HbA1c reduction of -1.99% 2
  • 12 mg: HbA1c reduction of -2.02% 2

Administration Details

Retatrutide is administered as a once-weekly subcutaneous injection, with pharmacokinetics supporting this dosing frequency 5, 3

The medication is currently in Phase 2 clinical trials and is not yet FDA-approved for clinical use 6, 1, 5

Safety Considerations

Gastrointestinal adverse events (nausea, diarrhea, vomiting) are dose-related and occur more frequently at higher doses, though most are mild to moderate in severity 1, 2, 3

Starting at lower doses (2 mg) and escalating gradually partially mitigates gastrointestinal side effects compared to starting at 4 mg 3

Dose-dependent increases in heart rate have been observed, peaking at 24 weeks and declining thereafter, with increases up to 6.7 beats/min 1, 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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