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Cancer & Diagnostics
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Clinical

Motixafortide

Also known as: Aphexda, BL-8040, BKT140

A cyclic peptide CXCR4 antagonist used with filgrastim to mobilize stem cells in multiple myeloma. FDA-approved as Aphexda (2023). Hospital medication.

Last updated

Mechanism of Action

Motixafortide is a synthetic cyclic peptide that binds the CXCR4 chemokine receptor with high affinity and slow dissociation. CXCR4 and its ligand CXCL12 (SDF-1) anchor hematopoietic stem cells in the bone marrow; blocking this interaction releases stem cells into the blood. Combined with G-CSF (filgrastim), it increases the number of CD34+ cells that can be collected by apheresis for autologous transplant.

Half-life
~2 hours
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Stem cell mobilization before autologous transplant in multiple myeloma
  • More patients reached collection targets in fewer apheresis sessions (GENESIS)
  • Used together with filgrastim

Potential Side Effects

  • Injection-site reactions (pain, redness, itching)
  • Pruritus, flushing and back pain
  • Anaphylactic shock and hypersensitivity reactions (label warning; premedication used)

Common Dosing

Aphexda is given by clinicians as a single weight-based subcutaneous injection after several days of filgrastim, timed before apheresis, with premedication to reduce reactions; a second dose may be given if needed. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • History of serious hypersensitivity to motixafortide
  • Not for mobilizing leukemic cells (label limitation)

No documented stacking partners for Motixafortide yet.

  • Motixafortide and G-CSF to mobilize hematopoietic stem cells for autologous transplantation in multiple myeloma: a randomized phase 3 trial

    2023

    View
  • Motixafortide: First Approval

    2023

    View

Yes. The FDA approved motixafortide as Aphexda in September 2023, in combination with filgrastim, to mobilize hematopoietic stem cells for collection and autologous transplantation in patients with multiple myeloma.

Both block CXCR4, but motixafortide is a peptide with longer receptor occupancy, while plerixafor is a small molecule. They have not been compared head to head in a large randomized trial; GENESIS compared motixafortide plus filgrastim with placebo plus filgrastim.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.