Research Chemical Designation & Liability
Compounds indexed in the MinMaxMuscle archive are strictly for laboratory research and development. They are NOT approved for human consumption. Theoretical dosing data is aggregated from clinical literature and must not be construed as medical instruction. Professional medical consultation is mandatory prior to any research application.
Pegbelfermin
Metabolic & Weight Loss
Molecular Dossier
- Rank Index: 48
- Status: Phase 2 Clinical
- What does this mean?
- Molecular Structure: MW: ~42 kDa (FGF-21 + PEG) | PEGylated protein analogue
About Pegbelfermin
Pegbelfermin (BeiGene, formerly Intercept) is a PEGylated FGF-21 analogue designed for sustained hepatic signaling. Phase 2b trials in MASH patients showed liver fat reduction and improvement in fibrosis markers. Unlike efruxifermin (Roche's fatty-acid conjugate), pegbelfermin uses polyethylene glycol conjugation for half-life extension. Phase 2 trials in alcoholic liver disease (ALD) and NASH are ongoing as of May 2026. Once-weekly or every-two-weeks subcutaneous injection. The FGF-21 mechanism is particularly attractive for MASH because it activates PPARγ-like signaling, improving adiponectin and reducing hepatic inflammation without appetite suppression.
Clinical Focus
PEG-Conjugated FGF-21 — Liver-Targeted Metabolic Therapy
Archival Aliases
BEI011, FGF-21-PEG, Intercept FGF-21
Frequently Asked Questions
Clinical Data Matrix
| Parameter | Clinical Value |
|---|---|
| Molecular Weight | MW: ~42 kDa (FGF-21 + PEG) | PEGylated protein analogue |
| Primary Pathway | Metabolic & Weight Loss |
| Research Phase | Phase 2 Clinical |
Clinical Pros
- Highly selective receptor modulation
- Documented efficacy in Phase II trials
- Minimal systemic cross-reactivity
Research Limitations
- Limited long-term human data
- Strict storage and reconstitution requirements
- Potential for acute homeostatic feedback loops
Community Discussion
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Data Verified: 2026-05-07