Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Apo e(130-149) mimetic peptide is a synthetic peptide derived from amino acids 130–149 of the low-density lipoprotein (LDL) receptor-binding domain of apolipoprotein E (apoE). It is designed to mimic the functional receptor-binding region of native apoE, specifically the amphipathic helix important for receptor interaction. This peptide can bind to apoE cell surface receptors—such as LDLR and LRP-1—and retain functional activity similar to the full-length protein. It has demonstrated potent anti-inflammatory, neuroprotective, and barrier-stabilizing effects in preclinical models, including reduction of pro-inflammatory cytokines (TNF, IL-6) and blood-brain barrier (BBB) disruption after brain injury. The mechanism involves modulation of inflammatory signaling cascades (such as the CypA-NF-κB-MMP-9 pathway), positive modulation of protein phosphatase 2A (PP2A) activity via SET binding antagonism, and suppression of neuronal cell apoptosis. The peptide has been investigated in mouse models for conditions including brain injury, subarachnoid hemorrhage, blood-brain barrier dysfunction, and experimental asthma via LDLR-dependent pathways[1][2][3]. It remains in preclinical or early clinical development.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on apo e(130-149) mimetic peptide.