Teduglutide (Gattex/Revestive) Dosage Calculator
Teduglutide (brand names Gattex in the US, Revestive in Europe) is an FDA-approved recombinant analog of glucagon-like peptide-2 (GLP-2) manufactured by Takeda for the treatment of adults and pediatric patients (1 year and older) with short bowel syndrome (SBS) who are dependent on parenteral support.
2,500mcg · Daily
Summary: Add 0mL BAC water to your 5mg vial. Draw to < 0.1 units on a U-100 syringe for a 2,500mcg dose. This vial will last 0 doses.
Cycle Planner
Teduglutide (Gattex/Revestive) Pharmacokinetics
Pharmacokinetics — Active Dose Over Time
t½ = ~2 hours (1.3h in SBS patients; range 0.9-3h depending on body weight)Disclaimer: This curve is a simplified first-order exponential decay model. Actual pharmacokinetics vary based on injection site, individual metabolism, body composition, and other factors. Half-life values are approximate and based on available preclinical and clinical literature. Many research peptides lack formal human pharmacokinetic studies. This is for educational purposes only — not medical advice.
Teduglutide (Gattex/Revestive) Dosing Protocol
| Level | Dose / Injection | Frequency |
|---|---|---|
| Beginner | 2,500mcg | Daily |
| Moderate | 3,500mcg | Daily |
| Aggressive | 5mg | Daily |
Note: FDA-approved GLP-2 analog for short bowel syndrome-associated intestinal failure. Weight-based dosing at 0.05 mg/kg/day SC. Supplied as 5mg lyophilized powder; reconstitute with 0.5mL sterile water for injection (10 mg/mL). Reduce dose to 0.025 mg/kg/day in patients with moderate-to-severe renal impairment (eGFR <60). Colonoscopy required within 6 months before starting treatment and at least every 5 years thereafter.
About Teduglutide (Gattex/Revestive)
Teduglutide (brand names Gattex in the US, Revestive in Europe) is an FDA-approved recombinant analog of glucagon-like peptide-2 (GLP-2) manufactured by Takeda for the treatment of adults and pediatric patients (1 year and older) with short bowel syndrome (SBS) who are dependent on parenteral support. It is a 33-amino acid peptide identical to native human GLP-2 except for a single substitution at position 2 (glycine replaced with alanine), which confers resistance to dipeptidyl peptidase-IV (DPP-IV) cleavage and extends the half-life to approximately 2 hours — enabling once-daily subcutaneous dosing. In the pivotal STEPS trial, 63% of patients receiving teduglutide 0.05 mg/kg/day achieved a clinically meaningful 20-100% reduction in parenteral support volume at 24 weeks, compared with 30% on placebo (p=0.002). Long-term extension studies (STEPS-2 and STEPS-3) demonstrated sustained reductions in parenteral nutrition requirements over 2+ years of continuous treatment.