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NCT06033001

Expanded Access Treatment with [Lu-177]-PNT2002 for Adult Patients with Prostate-Specific Membrane Antigen (PSMA)-Positive Metastatic Castration-Resistant Prostate Cancer (mCRPC)

TEMPORARILY NOT AVAILABLE Last updated 13 January 2025
What this trial tests

trial testing [Lu-177]-PNT2002 in Castration-Resistant Prostatic Cancer. Temporarily not available.

Quick facts

Lead sponsorLantheus Medical Imaging
StatusTEMPORARILY NOT AVAILABLE
Study typeEXPANDED_ACCESS
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Lantheus Medical Imaging — full company profile →

Who can join

18 and older, male only, with Castration-Resistant Prostatic Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this program is to provide access to \[Lu-177\]-PNT2002 to patients who have been diagnosed with prostate-specific membrane antigen (PMSA)-positive castration-resistant prostate cancer (mCRPC). Patients must have received at least 1 prior androgen pathway inhibitor (ARPI) and cannot be treated by currently available drugs or clinical trials. In this program participants will be administered \[Lu-177\]-PNT2002 intravenously every 8 weeks (about every 2 months) for 4 cycles, or 8 months of total treatment. During treatment, participants will be monitored with routine laboratory tests such as: * Hematology blood tests * Clinical Chemistry blood tests * Testosterone/Prostate Antigen levels blood test * Vital signs * Imaging * ECG

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Castration-Resistant Prostatic Cancer

Currently open trials in the same condition.

Other Lantheus Medical Imaging trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06033001.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing