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Trevogrumab Dosing Calculator

Trevogrumab (REGN1033): anti-myostatin antibody by Regeneron for lean mass preservation during GLP-1 weight loss.

Pre-filled with the most-reported clinical reconstitution protocol for Trevogrumab. See how 1 mL and 2 mL of bacteriostatic water change concentration and syringe-draw volume, then adjust the calculator below for your own vial.

Quick answer · Clinical protocol

A 15 mg vial of Trevogrumab reconstituted with 2 mL of bacteriostatic water yields a concentration of 7.50 mg/mL. At that concentration, a 200 mg dose of Trevogrumab equals 2666.7 units on a U-100 insulin syringe (26.667 mL). Trevogrumab is typically administered once daily.

Trevogrumab reconstitution: 1 mL vs 2 mL bac water

Bacteriostatic water volume is flexible. Less water means higher concentration and smaller injection volumes; more water means lower concentration and easier dose precision. Both options below are valid for a 15 mg vial.

BAC water addedConcentrationVolume per 200 mg doseDraw on U-100 syringe (units)
1 mL15.00 mg/mL13.333 mL1333.3 units
2 mL7.50 mg/mL26.667 mL2666.7 units
Based on a 15 mg vial of Trevogrumab reconstituted with bacteriostatic water. Insulin-syringe units assume a standard U-100 syringe (100 units = 1 mL).

Calculate your Trevogrumab dose

Alternative Trevogrumab protocols

Beyond the default above, Trevogrumab is also reported in the following protocols. Use these as starting points and recalculate with the tool above.

COURAGE Phase 2 Trial Protocol

Community
Dose
Dose details from ongoing trial
Frequency
Every 4 weeks
Duration
26 weeks (interim) to 52 weeks (full trial)
Route
Subcutaneous injection

Phase 2 combination trial with semaglutide; not yet commercially available

Obesity Triplet Therapy (COURAGE Phase 2, with Garetosmab)

Clinical
Dose
Trevogrumab 400 mg SC + garetosmab 10 mg/kg IV in combination with semaglutide 2.4 mg SC weekly. At 26 weeks, the triplet preserved 80.9% of lean mass and increased fat loss 27.3% vs semaglutide alone, but had a 28.3% discontinuation rate.
Frequency
Subcutaneous (trevogrumab) + IV (garetosmab) + SC weekly (semaglutide)
Duration
26-week weight-loss phase

The triplet therapy showed superior lean mass preservation and fat loss but had significantly higher discontinuation rates (28.3% vs 4-10% in other groups) and two deaths. This arm may not advance in its current form.

Phase 1 Dose-Finding (Postmenopausal Women)

Clinical
Dose
Single and multiple doses of trevogrumab SC alone or in combination with escalating doses of garetosmab IV. Dose-dependent increases in MRI-quantitated thigh muscle volume observed with combination therapy.
Frequency
Single dose and multiple-dose regimens tested
Duration
Variable duration across two study parts

Phase 1 trial (NCT02943239) in 82 subjects. Specific doses tested not fully disclosed in public reports. Combination blockade showed greater muscle gains than either antibody alone.

COURAGE Weight-Maintenance Phase

Clinical
Dose
After the 26-week weight-loss phase, participants are randomized to higher-dose trevogrumab monotherapy or placebo through week 52. This phase evaluates whether trevogrumab alone can maintain body composition improvements without concurrent semaglutide.
Frequency
Higher-dose trevogrumab SC monotherapy
Duration
26 weeks (weeks 27-52)

Results from the weight-maintenance phase have not been reported. This phase will provide important data on trevogrumab's standalone effects on lean mass and body composition.

Trevogrumab reconstitution & storage

Trevogrumab is supplied as a sterile solution for subcutaneous injection in clinical trial settings. The formulation is designed for SC administration and does not require reconstitution by end users. All preparation and administration occurs within clinical trial sites.

As a monoclonal antibody, trevogrumab requires refrigerated storage (2-8 degrees C) and protection from light. It must not be frozen. Storage and handling are managed by clinical trial sites per sponsor protocols. The drug is not available for self-administration or home storage outside of clinical trials.

Trevogrumab dosing FAQ

How much bacteriostatic water should I add to a 15 mg vial of Trevogrumab?

The community standard is 2 mL of bacteriostatic water for a 15 mg Trevogrumab vial. That gives a concentration of 7.50 mg/mL, so a 200 mg dose is 2666.7 units on a U-100 insulin syringe. Adding 1 mL instead doubles the concentration to 15.00 mg/mL and halves the draw to 1333.3 units. Less water = smaller injection volume but harder to measure precisely.

How many syringe units is a 200 mg dose of Trevogrumab?

On a standard U-100 insulin syringe, a 200 mg dose of Trevogrumab is 2666.7 units when the 15 mg vial is reconstituted with 2 mL of bacteriostatic water (7.50 mg/mL). If you use 1 mL of bac water instead, draw 1333.3 units (15.00 mg/mL).

What is the standard Trevogrumab dose?

Clinical protocols for Trevogrumab typically use 200 mg–400 mg once daily via subcutaneous injection. 200 mg is a common starting dose. Both 200 mg and 400 mg doses showed similar lean mass preservation (50.8% vs 51.3%). The higher dose showed modestly greater weight loss and fat loss. Specific dosing interval (Q2W or Q4W) should be confirmed from full trial publication.

Where do you inject Trevogrumab?

Trevogrumab is typically administered subcutaneously. Common subcutaneous sites are the lower abdomen (at least an inch from the navel), the outer thigh, and the love handles. Rotate sites with each injection to reduce localized irritation and bruising.

Can I use sterile water instead of bacteriostatic water for Trevogrumab?

Bacteriostatic water (containing 0.9% benzyl alcohol as a preservative) is strongly preferred for multi-dose vials like Trevogrumab because it inhibits microbial growth and lets a single vial be used over multiple weeks. Sterile water has no preservative and should generally be reserved for single-use preparations only.

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This website is for educational and informational purposes only. The information provided is not intended to diagnose, treat, cure, or prevent any disease. Always consult with a qualified healthcare professional before using any peptide or supplement.