Retatrutide

Description

• Certificate of Analysis
• HPLC
• Mass Spectrometry

Retatrutide: The Next Generation Triple-Agonist Therapy for Weight Loss (Phase 3)

Retatrutide is an investigational, first-in-class triple-agonist therapy currently in Phase 3 clinical trials. Developed by Eli Lilly, this cutting-edge injectable medication targets three metabolic hormone receptors—GLP-1 (glucagon-like peptide-1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon—to deliver unprecedented effects on weight loss, glucose control, and energy metabolism.

Mechanism of Action: Triple Hormone Synergy

Retatrutide represents a major leap beyond existing GLP-1 and GIP dual agonists like Tirzepatide. Its three-hormone activation approach is designed to deliver enhanced metabolic outcomes through:

• GLP-1 activation – suppresses appetite, slows gastric emptying, and improves glucose regulation

• GIP activation – boosts insulin sensitivity and promotes efficient fat metabolism

• Glucagon receptor activation – increases resting energy expenditure and supports fat burning

Together, these actions help the body burn more fat while preserving lean muscle, providing a balanced and sustained weight loss effect.

Clinical Trial Data (SURMOUNT Phase 2 Results)

In the SURMOUNT-Phase 2 trial, Retatrutide demonstrated remarkable results compared to Tirzepatide (Mounjaro):

These findings suggest that Retatrutide may deliver 3–5% greater total weight loss and improved metabolic efficiency over currently approved GLP-1/GIP dual agonists.

Proposed Dosing & Administration

Administration:

• Form: Weekly subcutaneous injection (prefilled pen)

• Sites: Abdomen or thigh (rotate injection sites)

• Frequency: Once weekly, same day each week

Titration Schedule:

• Weeks 1–4: 2 mg

• Weeks 5–8: 4 mg

• Weeks 9–12: 6 mg

• Weeks 13–16: 8 mg

• Week 17+: 10 mg maintenance

A monthly maintenance dose is currently under evaluation for future convenience.

Potential Advantages Over Current Therapies

Retatrutide shows several key benefits compared to existing agents like Tirzepatide and Semaglutide:

• Greater Fat Loss: Up to 62% fat reduction (vs. 58% with Tirzepatide)

• Improved Liver Health: 22% higher reduction in liver fat content

• Increased Metabolic Rate: 15% boost in resting metabolic rate (RMR)

• Preserved Muscle Mass: Balanced fat loss with minimal muscle depletion

These combined effects position Retatrutide as a potential game-changer for obesity and metabolic disease treatment.

Safety & Tolerability

Interim safety data from clinical trials show Retatrutide is well-tolerated, with side effects similar to other incretin-based therapies.

⚠️ Warning: As with other GLP-1 receptor agonists, preclinical studies suggest a possible risk of thyroid C-cell tumors. Retatrutide should not be used in individuals with a history of medullary thyroid carcinoma (MTC) or MEN-2 syndrome.

Ideal Patient Profile

Best suited for:

• Individuals with BMI ≥35 and comorbidities

• Non-responders to GLP-1 or GLP-1/GIP dual agonists

• Patients requiring >15% total body weight reduction

Contraindicated for:

• History of thyroid cancer or MEN type 2

• Severe renal or hepatic impairment

Monitoring Guidelines

To ensure safety and optimal results, patients may require the following evaluations:

Baseline:

• Calcitonin level

• Thyroid ultrasound

• Pancreatic enzyme assessment

• Cardiac evaluation

Ongoing:

• Monthly weight and BMI tracking

• Quarterly metabolic blood panels

• Annual DEXA scans for body composition

Projected Pricing & Access

Pending FDA and MHRA approval, Retatrutide is expected to be priced between $1,200–$1,500 per month.
Likely approved indications will include:

• Obesity (BMI ≥30)

• Overweight with comorbidities (BMI ≥27)

• NASH with fibrosis

• Treatment-resistant Type 2 Diabetes

Access may require documentation of prior medication trials and lifestyle interventions.