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Healing & Recovery

Peptides studied in tissue-repair models — tendon, ligament, muscle, gut, skin and the vasculature — including BPC-157, TB-500, GHK-Cu, KPV and the combined blends, with the animal and early human literature behind each.

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Peptide profiles

6 research profiles in Healing & Recovery, listed alphabetically.

Compound Research area Overview Read the profile
BPC-157 A synthetic pentadecapeptide advancing from preclinical tissue-repair research into human trials. BPC-157 is a stable 15-amino-acid peptide studied for tendon, muscle, and gastrointestinal repair — now entering Phase 1 and Phase 2 human trials. Read →
BPC-157 + TB-500 (Repair Combo) The two leading tissue-repair peptides, paired for complementary mechanisms. A combination of BPC-157 and TB-500 — two complementary tissue-repair peptides. See each individual profile for mechanisms and human-trial status. Read →
GHK-Cu (Copper Peptide) A naturally occurring copper tripeptide with direct human trials in skin and wound repair. GHK-Cu, the copper tripeptide, is studied for collagen synthesis, wound healing, and skin repair — now in Phase 2 and Phase 4 human trials. Read →
KLOW (Peptide Repair Blend) A combination blend of GHK-Cu, BPC-157, TB-500, and KPV, formulated for tissue-repair research. KLOW is a combination blend of GHK-Cu, BPC-157, TB-500, and KPV — four peptides studied for tissue repair and anti-inflammatory activity. Read →
KPV (Lysine-Proline-Valine) The three-amino-acid tail of α-MSH that keeps the anti-inflammatory signal and drops the pigmentation. KPV is the C-terminal tripeptide of α-MSH, studied for NF-κB-mediated anti-inflammatory activity in colitis, airway and skin models, with well-characterized cellular uptake via the PepT1 transporter. Read →
TB-500 (Thymosin β-4) A Thymosin β-4 fragment — one of the more clinically advanced peptides in regenerative research. TB-500 reproduces the active region of Thymosin β-4, whose parent molecule has reached Phase 2 and Phase 3 human trials in cardiac, wound, and corneal repair. Read →

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