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  2. ›drugs
  3. ›PLUVICTO
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PLUVICTO

updated 3mo ago
by $NVS NOVARTIS AG🔗 ChEMBL
community read0 votes

🐶 often sniffed alongside

top 4
  • tagApproval18 co-mentions · 5 sources
  • druglutetium Lu 177 vipivotide tetraxetan12 co-mentions · 5 sources
  • tagOncology4 co-mentions · 1 sources
  • tagProstate Cancer4 co-mentions · 1 sources

Protein drug with a maximum clinical stage of Approval (across all indications), with an approval for prostate cancer and 6 investigational indications.

targets

Glutamate carboxypeptidase 2

all catalysts(0)

nothing on the calendar yet

Trials studying PLUVICTO

  • phase1A Study of Pasritamig (JNJ-78278343) in Combination With Other Agents for Metastatic Prostate Cancerrecruitingn=300
  • EP1A Dosimetry Study of Lutetium (177Lu) rhPSMA-10.1 and Lutetium (177Lu) Vipivotide Tetraxetan (Pluvicto®) in Patients With Non-curative Metastatic Prostate Cancerterminatedn=17

News(10)

  • ITM neuroendocrine tumor drug spurned by FDA over manufacturing qualms
    The FDA has denied ITM Isotopes Technologies’ lead pipeline candidate for a rare group of tumors due to qualms over the drug’s manufacturing.
    fiercebiotech · 5d ago
  • J&J pharma leader to retire; Krystal slumps on gene therapy miss
    Jennifer Taubert will step down after a lengthy run leading J&J’s pharmaceutical business. Elsewhere, pricing issues hampered what Wall Street analysts view as an otherwise strong gene therapy launch.
    biopharma_dive · 10d ago
  • FDA expands Pluvicto label, making it available to most metastatic prostate cancer patients
    The FDA approved Novartis’ radiopharma drug Pluvicto for use alongside hormone therapy, making the drug available to many more patients. The approval nearly doubles the eligible patient population…
    endpoints · 11d ago
  • Curium strikes up to $8B deal for radiopharma rival Lantheus
    Months after reports first linked Curium to a potential Lantheus takeover, the radiopharma players have made it official with a deal worth up to $8 billion.
    fiercebiotech · 11d ago
  • Recon: AstraZeneca, BMS discuss merger; FDA broadens indication for Novartis’ Pluvicto
    Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
    raps · 12d ago
  • Novartis scraps mid-stage radiopharma asset as Pluvicto soars
    The discontinued asset, being trialed for breast cancer and solid tumors, had yielded disappointing data, leading to Novartis’ decision to abandon development, according to a company spokesperson.
    biospace · 24d ago
  • Novartis climbs on upbeat drug sales as key readouts loom
    A return to quarterly sales growth boosted shares higher on Tuesday, though a handful of coming study results will have a bigger impact on the company’s long-term outlook.
    biopharma_dive · 24d ago
  • Novartis stays 'geography-agnostic' in dealmaking amid flurry of China deals
    Novartis will continue to be on the lookout for bolt-on deals below $2 billion, CEO Vas Narasimhan said Tuesday on the pharma's second quarter earnings call—though major pickups aren’t completely o…
    biospace · 24d ago
  • Novartis drops phase 2 radioligand therapy, but CEO’s commitment to modality ‘unchanged’
    Novartis has dropped a phase 2-stage radioligand therapy after the candidate disappointed in the clinic.
    fiercebiotech · 25d ago
  • Radiopharma maker AdvanCell hauls in $315M for Pluvicto challenger
    AdvanCell raised a $315 million Series D to study a lead-based prostate cancer agent and shore up its US manufacturing of the radioactive treatment. The round marks one of the largest yet for a rad…
    endpoints · 1mo ago
view all news mentions →
brand
PLUVICTO
trade names
Pluvicto
generic
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN
MOA
12.1 Mechanism of Action Lutetium Lu 177 vipivotide tetraxetan is a radioligand therapeutic agent. The active moiety of lutetium Lu 177 vipivotide tetraxetan is the radionuclide lutetium-177 which is linked to a moiety that binds to PSMA, a transmembrane protein that is expressed in prostate cancer, including mCRPC. Upon binding of lutetium Lu 177 vipivotide tetraxetan to PSMA-expressing cells, the beta-minus emission from lutetium-177 delivers radiation to PSMA-expressing cells, as well as to surrounding cells, and induces DNA damage which can lead to cell death.
indication
1 INDICATIONS AND USAGE PLUVICTO is indicated for the treatment of adult patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor pathway inhibitor (ARPI) therapy, and are considered appropriate to delay taxane-based chemotherapy, or have received prior taxane-based chemotherapy. PLUVICTO is a radioligand therapeutic agent indicated for the treatment of adult patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor pathway inhibitor (ARPI) therapy, and are considered appropriate to delay taxane-based chemotherapy, or have received prior taxane-based chemotherapy. ( 1 )
Data sources
ClinicalTrials.gov · OpenTargets
last refreshed 10m ago
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