Real-World data reveals early use of prostate cancer drug in thousands of patients
NCT ID NCT07450157
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study examined medical records of over 6,400 prostate cancer patients who received a treatment called 177Lu-PSMA-617. Researchers wanted to understand the patients' characteristics, treatment patterns, and survival outcomes. The study did not test a new treatment but instead analyzed existing data to see how the drug was being used in real-world settings.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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6,448 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Feb 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with electronic health care records in multiple databases who were treated with 177Lu-PSMA-617.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Phase I inclusion criteria: 1. Patients with ≥1 claim in the open-source medical claims data with a Healthcare Common Procedure Coding System (HCPCS) code of A9607 or ≥1 claim in the open-source medical or pharmacy claims data with a National Drug Code (NDC) code for 177Lu-PSMA-617 during the patient selection window. The date of the first such claim is the index date. 2. For patients identified via NDC code, ≥1 claim with one of the following procedure codes on the same date as the 177Lu-PSMA-617 NDC claim: HCPCS - A9699, J3590; CPT 79191; or ≥1 claim with HCPCS code A9595 or A9597 occurring within 14 days before or after the index date. 3. At least 18 years of age at index date. 4. Patients with ≥2 medical claims ≥180 days prior to the index date. For the treatment response analysis, the following additional criteria were applied: 5. Patients with linkage to lab data. 6. Patients with ≥1 PSA result available on or within 6 months prior to the index date. The PSA result closest to the index date was defined as the baseline PSA level. 7. Patients with ≥1 PSA result available after the index date. Phase II inclusion criteria: 1. ≥2 medical claims (≥30 days apart) with a diagnosis of prostate cancer observed during the patient selection period. 2. ≥1 medical claim with a diagnosis code for metastatic disease occurring on or after the first observed prostate cancer diagnosis. The date of the first such claim was defined as the date of metastasis. 3. Evidence of castration resistance observed during the study period. The date of mCRPC diagnosis was defined as the latest of the date of metastasis and the date of castration resistance and must have occurred during the index window. 4. ≥12 months of continuous data availability prior to the mCRPC diagnosis date. 5. ≥1 claim for 177Lu-PSMA-617 after mCRPC diagnosis and continuous data availability between diagnosis and the date of 177Lu-PSMA-617 initiation. Exclusion criteria 1\. Standard data cleaning processes were applied to remove patients with data quality issues. Specific data quality issues included missing or invalid age or sex.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Novartis
East Hanover, New Jersey, 07936, United States
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Other studies related to the condition(s) this trial covers.
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