degarelix
Drugsubcutaneous
Other names: ASP3550
NCT Number: NCT01964170
To compare the efficacy and safety of ASP3550 to goserelin acetate in patients with prostate cancer.
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Notify Me20 year and older
Male
Interventional
Phase 3
Chugoku, Japan
This study consists of two parts. The purpose of PART 1 is to test non-inferiority of ASP3550 to goserelin acetate with respect to the cumulative castration rate in terms of serum testosterone when ASP3550 or goserelin acetate is administered for one-year in patients with prostate cancer.
The patients assigned to receive ASP3550 and completed the treatment in PART 1 are eligible for the treatment in PART 2, and will receive ASP3550 maintenance dose subcutaneously for additional term. The long-term safety, efficacy and PK of the continued ASP3550 treatment will be assessed in PART 2.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
subcutaneous
Other names: ASP3550
subcutaneous
Time frame: Up to one year of the treatment
Time frame: Up to one year of the treatment
Time frame: Baseline and Days 3, 7, and 28
Time frame: Up to one year of the treatment
Time frame: up to the end of treatment. approximately for 2 years
Astellas Pharma Inc
Industry
ASP3550 Phase III Study - An Open-Label, Active-Controlled, Parallel-Arm Study, Comparing ASP3550 With Goserelin Acetate in Patients With Prostate Cancer -
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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