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Last Updated: May 10, 2024

CLINICAL TRIALS PROFILE FOR HISTRELIN ACETATE


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All Clinical Trials for histrelin acetate

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01394263 ↗ Study of Histrelin Subdermal Implant in Patients With Prostate Cancer Completed Endo Pharmaceuticals Phase 3 2000-05-01 This trial was an open-label, multi-national, randomized, parallel treatment, active-control multicenter study in adult males with documented metastatic prostate cancer disease who were judged to be candidates for hormone therapy.
NCT01697384 ↗ Study to Evaluate Efficacy and Safety of Histrelin Subdermal Implant in Men With Advanced Prostate Cancer Completed Endo Pharmaceuticals Phase 3 2000-04-01 Objective was to evaluate the efficacy and safety of the histrelin acetate subdermal implant (originally versus Lupron Depot-3 Month) in male patients with advanced prostate cancer during 52 weeks of treatment with the implant. After consultation w/ FDA, design was modified to eliminate the Lupron arm and continued the study as an open-label non-randomized study. Primary endpoint was testosterone suppression, as assessed by the percent of patients whose testosterone indicated chemical castration levels (<=50 ng/dL) through 52 weeks of treatment with an implant.
NCT02278185 ↗ Enzalutamide Versus Standard Androgen Deprivation Therapy for the Treatment Hormone Sensitive Prostate Cancer Unknown status University of Colorado, Denver Phase 2 2015-11-11 This randomized phase II trial compares enzalutamide with standard androgen deprivation therapy in reducing incidence of metabolic syndrome in patients with prostate cancer that has spread to other places in the body. Metabolic syndrome is defined as changes in cholesterol, blood pressure, circulating sugar levels, and body weight. Previous studies have shown that patients with prostate cancer, who have been treated with standard medical therapy that lowers testosterone levels, have an increased risk of these changes. Hormone therapy using enzalutamide may fight prostate cancer by blocking the use of testosterone by the tumor cells instead of lowering testosterone levels. It is not yet known whether prostate cancer patients who receive enzalutamide will have reduced incidence of metabolic syndrome than patients who receive standard androgen deprivation therapy.
NCT03678025 ↗ Standard Systemic Therapy With or Without Definitive Treatment in Treating Participants With Metastatic Prostate Cancer Recruiting National Cancer Institute (NCI) Phase 3 2018-09-17 This phase III trial studies how well standard systemic therapy with or without definitive treatment (prostate removal surgery or radiation therapy) works in treating participants with prostate cancer that has spread to other places in the body. Addition of prostate removal surgery or radiation therapy to standard systemic therapy for prostate cancer may lower the chance of the cancer growing or spreading.
NCT03678025 ↗ Standard Systemic Therapy With or Without Definitive Treatment in Treating Participants With Metastatic Prostate Cancer Recruiting Southwest Oncology Group Phase 3 2018-09-17 This phase III trial studies how well standard systemic therapy with or without definitive treatment (prostate removal surgery or radiation therapy) works in treating participants with prostate cancer that has spread to other places in the body. Addition of prostate removal surgery or radiation therapy to standard systemic therapy for prostate cancer may lower the chance of the cancer growing or spreading.
NCT04513717 ↗ Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial Suspended National Cancer Institute (NCI) Phase 3 2020-12-15 This phase III trial compares less intense hormone therapy and radiation therapy to usual hormone therapy and radiation therapy in treating patients with high risk prostate cancer and low gene risk score. This trial also compares more intense hormone therapy and radiation therapy to usual hormone therapy and radiation therapy in patients with high risk prostate cancer and high gene risk score. Abiraterone acetate may help fight prostate cancer by lowering the amount of testosterone made by the body. Apalutamide may help fight prostate cancer by blocking the use of androgen by the tumor cells. Radiation therapy uses high energy rays to kill tumor cells and shrink tumors. Giving a shorter hormone therapy treatment may work the same at controlling prostate cancer compared to the usual 24 month hormone therapy treatment in patients with low gene risk score. Adding abiraterone acetate and apalutamide to the usual treatment may increase the length of time without prostate cancer spreading as compared to the usual treatment in patients with high gene risk score.
NCT04513717 ↗ Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial Suspended NRG Oncology Phase 3 2020-12-15 This phase III trial compares less intense hormone therapy and radiation therapy to usual hormone therapy and radiation therapy in treating patients with high risk prostate cancer and low gene risk score. This trial also compares more intense hormone therapy and radiation therapy to usual hormone therapy and radiation therapy in patients with high risk prostate cancer and high gene risk score. Abiraterone acetate may help fight prostate cancer by lowering the amount of testosterone made by the body. Apalutamide may help fight prostate cancer by blocking the use of androgen by the tumor cells. Radiation therapy uses high energy rays to kill tumor cells and shrink tumors. Giving a shorter hormone therapy treatment may work the same at controlling prostate cancer compared to the usual 24 month hormone therapy treatment in patients with low gene risk score. Adding abiraterone acetate and apalutamide to the usual treatment may increase the length of time without prostate cancer spreading as compared to the usual treatment in patients with high gene risk score.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for histrelin acetate

Condition Name

Condition Name for histrelin acetate
Intervention Trials
Adenocarcinoma of the Prostate 3
Stage IVA Prostate Cancer AJCC v8 2
Prostate Cancer 2
Metastatic Prostatic Adenocarcinoma 1
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Condition MeSH

Condition MeSH for histrelin acetate
Intervention Trials
Prostatic Neoplasms 5
Adenocarcinoma 4
Neoplasms 1
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Clinical Trial Locations for histrelin acetate

Trials by Country

Trials by Country for histrelin acetate
Location Trials
United States 69
Mexico 1
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Trials by US State

Trials by US State for histrelin acetate
Location Trials
Louisiana 2
Colorado 2
Massachusetts 2
Michigan 2
Iowa 2
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Clinical Trial Progress for histrelin acetate

Clinical Trial Phase

Clinical Trial Phase for histrelin acetate
Clinical Trial Phase Trials
Phase 3 4
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for histrelin acetate
Clinical Trial Phase Trials
Completed 2
Suspended 1
Unknown status 1
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Clinical Trial Sponsors for histrelin acetate

Sponsor Name

Sponsor Name for histrelin acetate
Sponsor Trials
National Cancer Institute (NCI) 2
Endo Pharmaceuticals 2
University of Colorado, Denver 1
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Sponsor Type

Sponsor Type for histrelin acetate
Sponsor Trials
Other 3
NIH 2
Industry 2
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