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Peptide Therapy GuideClear peptide education

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Body Recomposition Peptides 2026 Update: Compound Comparison

Below is a comparison of the peptides most commonly referenced in body recomposition research as of 2026. This table synthesizes published trial data, documented mechanisms, and practical considerations. Survodutide GLP-1/glucagon dual agonist. Enhances lipoly

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This page preserves a source comparison for education. It does not add a rating, recommendation or clinical judgment.

  • Below is a comparison of the peptides most commonly referenced in body recomposition research as of 2026. This table synthesizes published trial data, documented mechanisms, and practical considerations.
  • Survodutide
  • GLP-1/glucagon dual agonist. Enhances lipolysis while preserving mTOR signaling in muscle tissue
  • +2.1% lean mass vs baseline (Phase III)
  • −14.3% total body weight, ~92% from fat
  • Subcutaneous injection, weekly
  • Strongest evidence for lean tissue preservation during aggressive deficit. Nausea common during titration.
  • Mazdutide
  • GLP-1/GIP/glucagon tri-agonist. Amino acid partitioning favors muscle over adipose
  • +1.8% lean mass despite 16.8% total weight loss
  • −16.8% body weight, 85% adipose tissue
  • Superior fat-to-lean ratio in clinical trials. GIP component may enhance insulin sensitivity more than survodutide.
  • Follistatin-344
  • Myostatin antagonist. Blocks GDF-8 inhibition of satellite cell proliferation
  • +3.2kg lean mass in older adults without structured training
  • Minimal direct fat loss (indirect via increased RMR)
  • Intramuscular injection, bi-weekly
  • Requires pharmaceutical-grade sourcing. Most effective in populations with elevated baseline myostatin.
  • CJC-1295 + Ipamorelin
  • GHRH analog + selective GH secretagogue. Increases endogenous GH and IGF-1
  • +1.6–2.2kg lean mass with resistance training
  • −3.8% body fat percentage over 16 weeks
  • Subcutaneous injection, daily or 5 days/week
  • Effect amplifies training stimulus but doesn't replace it. Minimal impact without structured hypertrophy protocol.
  • MK 677
  • Non-peptide ghrelin mimetic. Oral GH secretagogue
  • +1.2–1.8kg lean mass over 6 months
  • Modest (−2.1% body fat)
  • Oral capsule, once daily
  • Oral bioavailability is the advantage. Insulin resistance risk above 25mg/day. Water retention common.