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OncologyIn Clinical Trials

Vantictumab

Intravenous
Written by Peptide Association Editorial TeamMedically reviewed by Ian Justl Ellis, MD, CPTLast reviewed Editorial policy

Overview

Vantictumab is a fully human monoclonal antibody that targets multiple Frizzled receptors involved in the Wnt signaling pathway. By blocking Frizzled receptors 1, 2, 5, 7, and 8, it inhibits Wnt-driven tumor growth and is designed to target cancer stem cells.

Mechanism of Action

The therapeutic rationale is based on dysregulated Wnt signaling in various solid tumors, particularly breast and pancreatic cancers. Inhibition of this pathway may reduce tumor recurrence and metastatic potential.

Research Summary & Key Findings

Phase I trials in solid tumors demonstrated dose-limiting bone toxicity including fractures, which restricted further development. A phase Ib study in metastatic pancreatic cancer combined with chemotherapy was terminated early due to safety concerns (2016). Despite promising preclinical activity against cancer stem cells, clinical development has been halted.

Clinical Status

In Clinical Trials

Vantictumab is currently undergoing clinical trials. It is not yet FDA-approved and is available only through clinical research settings or investigational protocols.

Administration Routes

Intravenous

References

Primary literature

Study-level citations for this compound are being verified against the primary sources before publication. The database queries above return the current indexed literature in the meantime.

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Disclaimer: This information is provided for educational and research purposes only. It is not intended as medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before starting any peptide therapy. The Peptide Association does not endorse or recommend any specific treatment protocol. See our editorial policy for how this content is produced and reviewed.