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ClinicalMuscleOtherMonthly (trial)

Bimagrumab

BYM338

Fully human mAb against activin type-II receptors. Failed sarcopenia and sIBM endpoints; now developed by Lilly for obesity in combination with tirzepatide (BELIEVE trial).

◆ Editorial note

Fully human IgG1 monoclonal antibody. Not a peptide.

§ 01   Overview

Overview

Fully human mAb against activin type-II receptors. Failed sarcopenia and sIBM endpoints; now developed by Lilly for obesity in combination with tirzepatide (BELIEVE trial).

Failed primary endpoints in sarcopenia and sIBM. BELIEVE Phase 2 tests combination with tirzepatide.

§ 02   Mechanism

Mechanism of action

Bimagrumab blocks ActRIIA/B to prevent myostatin, activin A, and GDF-11 signaling. It drives muscle hypertrophy with simultaneous fat loss, which makes it interesting as an obesity adjunct that preserves lean mass while GLP-1 class drives caloric deficit.

  • 01Increases lean mass + decreases fat mass simultaneously
  • 02Attractive for muscle-preserving obesity therapy

§ 03   Dosing

Dosing protocol

Standard Protocol

Dose Range
10 mg/kg IV (trial)
Route
Other
Frequency
Monthly (trial)

§ 04   Evidence

Evidence & research

Clinical

Failed primary endpoints in sarcopenia and sIBM. BELIEVE Phase 2 tests combination with tirzepatide.

FDA Status

Not FDA-approved. In development for obesity in combination.

§ 06   News

In the news

8 articles from the last 12 months · updates hourly

§ 07   Sourcing

Sourcing & supply

Regulatory status

Investigational, no compounding path

Currently in active clinical trials. No compounding pathway. No brand product. The only US channels are RUO vendors that the FDA has targeted with warning letters. Assume any sourcing carries significant regulatory and quality risk.

No suppliers in our directory currently stock this compound. For investigational or research-only compounds, legitimate channels may not exist outside clinical trials.

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§ 09   Safety

Safety & side effects

Side effects

  • 01Muscle spasms
  • 02Diarrhea
  • 03Injection site reactions

Contraindications

None specified.

§ 10   Questions

Bimagrumab FAQ

What is Bimagrumab?
Fully human mAb against activin type-II receptors. Failed sarcopenia and sIBM endpoints; now developed by Lilly for obesity in combination with tirzepatide (BELIEVE trial). Bimagrumab blocks ActRIIA/B to prevent myostatin, activin A, and GDF-11 signaling. It drives muscle hypertrophy with simultaneous fat loss, which makes it interesting as an obesity adjunct that preserves lean mass while GLP-1 class drives caloric deficit.
What is Bimagrumab used for?
Reported uses include increases lean mass + decreases fat mass simultaneously and attractive for muscle-preserving obesity therapy. Evidence strength is rated Clinical — see the evidence section for detail.
How is Bimagrumab dosed?
Commonly referenced dosing is 10 mg/kg IV (trial), typically monthly (trial), administered Other. This is educational reference only; consult a licensed clinician before use.
What are the side effects of Bimagrumab?
Commonly reported side effects include muscle spasms, diarrhea, and injection site reactions. This list is not exhaustive.
Is Bimagrumab legal?
Currently in active clinical trials. No compounding pathway. No brand product. The only US channels are RUO vendors that the FDA has targeted with warning letters. Assume any sourcing carries significant regulatory and quality risk. FDA status: Not FDA-approved. In development for obesity in combination..

§ 11   References

Selected references

  1. 01

    Rooks sarcopenia trial

    PMID: 28653345 (NCT02333331)

  2. 02

    sIBM long-term

    PMID: 32737152

  3. 03

    BELIEVE — tirzepatide combo

    NCT05616013

This site is for educational and research purposes only. It does not constitute medical advice. Always consult a qualified healthcare provider before using any peptide or supplement.