ABT-510

Thrombospondin 1 Mimetic NonapeptideRx: InvestigationalCompound: Investigational

Also known as: ABT-510, ABT‑510, thrombospondin mimetic, Thrombospondin‑1 mimetic peptide, TSP-1 mimetic peptide

Educational Only — Not medical advice. Consult a qualified clinician before using any peptide.

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Summary

ABT‑510 is a synthetic 9‑amino‑acid peptide that acts as an anti‑angiogenic agent by engaging the CD36 receptor, investigated in phase II oncology trials.

Mechanism of Action

Mimics the type I repeat of thrombospondin‑1 and binds CD36 on endothelial cells, suppressing VEGF‑driven angiogenesis

Routes of Administration

IntravenousSubcutaneous

Goals & Uses

  • Solid tumor treatmentOncologyLow
  • solid tumor cancer therapyOncologyModerate
  • anti‑angiogenic cancer therapyOncologyModerate
  • Tumor angiogenesis inhibitionOncology / AntiangiogenicModerate
  • ocular neovascular diseaseOphthalmologyLow
  • Combination antiangiogenic therapyOncology / CombinationLow

Contraindications

  • known hypersensitivity to peptideImmunologicModerate
  • Known hypersensitivity to ABT-510 or peptide excipientsAllergyHigh
  • hypersensitivity to peptide componentsAllergyModerate
  • PregnancyPopulationHighPotential fetal risk or insufficient safety data

Adverse Effects

  • HypertensionCardiovascularUncommonHigh blood pressure
  • Injection site reactionsLocalCommon
  • Injection site painLocalCommonPain at the injection site
  • ThrombocytopeniaHematologicUncommonLow platelet count
  • NauseaGastrointestinalUncommonFeeling of sickness or urge to vomit
  • FatigueGeneralCommonLow energy or tiredness
  • Injection site erythemaLocalCommonRedness at the injection site

Drug Interactions

  • Cytotoxic chemotherapy agentsModerate
  • none identifiedLow
  • Anticoagulants / antiplatelet agentsModerate
  • other anti‑angiogenic agents (e.g., bevacizumab)Moderate

Population Constraints

  • Severe hepatic or renal impairmentOrgan ImpairmentRelative
  • Pediatric patientsAgeRelative
  • Pregnant or lactating womenReproductiveAbsolute
  • Pregnant womenReproductiveAbsolute

Regulatory Status

  • European UnionInvestigationalUnder clinical investigation; not authorized
  • United StatesInvestigationalInvestigational New Drug (IND) status; no FDA approval
  • United KingdomInvestigationalNo marketing authorization

Not approved by FDA or EMA; studied in Phase II trials for melanoma, renal cell carcinoma, and sarcoma.

Evidence & Sources

No sources recorded yet.

Frequently Asked Questions

What is ABT-510?

ABT‑510 is a synthetic 9‑amino‑acid peptide that acts as an anti‑angiogenic agent by engaging the CD36 receptor, investigated in phase II oncology trials.

What is ABT-510 used for?

ABT-510 is educationally associated with: Solid tumor treatment, solid tumor cancer therapy, anti‑angiogenic cancer therapy, Tumor angiogenesis inhibition, ocular neovascular disease, Combination antiangiogenic therapy. Educational only — not medical advice.

How is ABT-510 administered?

Recorded routes of administration: Intravenous, Subcutaneous.

What are the potential side effects of ABT-510?

Reported adverse effects include: Hypertension, Injection site reactions, Injection site pain, Thrombocytopenia, Nausea, Fatigue, Injection site erythema. This list is not exhaustive — consult a qualified clinician.

Who should avoid ABT-510?

Recorded contraindications: known hypersensitivity to peptide, Known hypersensitivity to ABT-510 or peptide excipients, hypersensitivity to peptide components, Pregnancy. Consult a qualified clinician before use.