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Lutetium Lu-177 vipivotide tetraxetan

Lutetium Lu 177 vipivotide tetraxetan is a PSMA-targeted radioligand that carries therapeutic radiation to selected prostate-cancer cells.

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At a glance

Evidence stage
Approved use
Regulatory status
PLUVICTO has FDA-approved PSMA-positive metastatic prostate-cancer indications, including a July 2026 expansion to androgen-pathway-modulation-naive/sensitive disease with ARPI therapy.
Research context
Lutetium Lu 177 vipivotide tetraxetan is a PSMA-targeted radioligand that carries therapeutic radiation to selected prostate-cancer cells.

What this is

  • Lutetium Lu 177 vipivotide tetraxetan is a PSMA-targeted radioligand that carries therapeutic radiation to selected prostate-cancer cells.

What this isn't

  • A recommendation to use, prepare, combine, or administer a product
  • Evidence that a related molecule or a differently formulated product has the same effects

Key terms

Lutetium Lu 177 vipivotide tetraxetan is a PSMA-targeted radioligand that carries therapeutic radiation to selected prostate-cancer cells.

The targeting component binds prostate-specific membrane antigen, while lutetium-177 delivers beta radiation that damages nearby cells. Selection depends on PSMA imaging and the clinical disease state. This is a radiopharmaceutical, not an interchangeable supplement peptide; it is also distinct from lutetium-177 products targeting somatostatin receptors in other tumors. Current FDA prescribing information.

Evidence limits

How to read the evidence

The July 2026 FDA expansion is broader than older summaries restricted to resistant disease after prior therapies. Nevertheless, PSMA positivity, disease category, and accompanying therapy remain essential boundaries. The reported progression endpoint should not be restated as established overall-survival improvement or cure, and the interim follow-up cannot define every late radiation-related risk. FDA expansion announcement; trial report.

Sources appraised 2026-10-28. Educational information; not medical advice. Study findings apply to the populations, preparations and outcomes described.

External sources and citations

  1. PLUVICTO FDA prescribing information, July 2026
  2. FDA July 2026 PLUVICTO indication expansion
  3. PSMAddition randomized phase 3 results

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