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NCE-1 Intelligence & Market Opportunity

Pluvicto

Lutetium (177lu) Vipivotide Tetraxetan
Anticancer
Intravenous Solution

Pluvicto turned an unusually clean target into a therapy: prostate cancer expresses PSMA densely and almost uniquely, making it well suited to delivering radiation systemically.

It binds PSMA on tumor cells and delivers beta-emitting lutetium-177 directly to them, largely sparing healthy tissue. Given intravenously every six weeks, it treats adults with PSMA-positive metastatic castration-resistant prostate cancer previously treated with androgen receptor pathway inhibition and taxane-based chemotherapy.

Pluvicto’s launch was constrained by radiopharmaceutical manufacturing and supply capacity rather than demand, and it has since expanded into pre-chemotherapy use. Requiring companion PSMA PET imaging and nuclear medicine infrastructure, it is the reference asset for the radioligand therapy field.

Approval Date
23-Mar-22
NCE-1 Date
23-Mar-26
NCE Date
23-Mar-27
Commercial snapshot

Market performance & projections

Revenue ($M)
1,994
CAGR (%)
28.37%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
3,373
2027
4,183
2028
4,880
2029
5,415
2030
5,893
2031
6,379
2032
6,837
Molecule profile

Details & specifications

Molecule
Lutetium (177lu) Vipivotide Tetraxetan
Innovator
NOVARTIS PHARMACEUTICALS CORPORATION
Dosage Form
Intravenous Solution
Strength
27 mCi/mL
Therapeutic Category
Anticancer
Usage
To treat prostate-specific membrane antigen-positive metastatic castration-resistant prostate cancer following other therapies
Good to know

Frequently asked questions

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