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Completed

NCT Number: NCT01964170

A Study to Compare the Effect of ASP3550 With Goserelin in Patients With Prostate Cancer

To compare the efficacy and safety of ASP3550 to goserelin acetate in patients with prostate cancer.

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Key information

Age range

20 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 3

Primary location

Chugoku, Japan

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male patient with histologically confirmed prostate cancer (adenocarcinoma).
  • Patient in whom endocrine treatment is indicated. Patient having undergoing prostatectomy or radiotherapy with curative intention and has a rising serum PSA (PSA ≥ 2 ng/mL at screening) may be included.
  • Has a serum testosterone level above 2.2 ng/mL at screening.
  • Has an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 0 to 2 at screening.
  • Has a serum PSA ≥ 2 ng/mL at screening.
  • Has a life expectancy of at least 12 months.

Exclusion criteria

  • Previous or present endocrine treatment for prostate cancer. Example: surgical castration, GnRH agonists, GnRH antagonists, antiandrogens or oestrogens, and 5α-reductase inhibitors.
  • Received a 5α-reductase inhibitor within 25 weeks preceding screening.
  • Is a candidate for curative therapy, i.e., radical prostatectomy or radiotherapy within 12 months.
  • Has concurrent or a history of poorly controlled severe asthma, anaphylactic reactions, severe urticaria or angioedema.
  • Has hypersensitivity towards mannitol.
  • Has a marked prolongation of QT/QTc interval (two consecutive increases to >450 ms in QTc interval at retest) at screening.
  • Has concurrent or a history of a disease (heart failure, hypokalemia, a family history of QT prolongation syndrome, etc.) that may induce Torsade de Pointes.

Treatment and study plan

degarelix

Drug

subcutaneous

Other names: ASP3550

Goserelin

Drug

subcutaneous

Primary outcomes

  1. Cumulative castration rate of treatment in terms of serum testosterone level

    Time frame: Up to one year of the treatment

Secondary outcomes

  1. Proportion of castrated subjects in terms of serum testosterone level

    Time frame: Up to one year of the treatment

  2. Proportion of castrated subjects in terms of serum testosterone level

    Time frame: Baseline and Days 3, 7, and 28

  3. Changes in serum levels of prostate-specific antigen (PSA) over time

    Time frame: Up to one year of the treatment

  4. Safety assessed by the incidence of adverse events

    Time frame: up to the end of treatment. approximately for 2 years

Sponsors and collaborators

Lead sponsor

Astellas Pharma Inc

Industry

Registry information

Official study title

ASP3550 Phase III Study - An Open-Label, Active-Controlled, Parallel-Arm Study, Comparing ASP3550 With Goserelin Acetate in Patients With Prostate Cancer -

Important dates

Study start
2013
Primary completion
2015
Study completion
2016
First posted
Oct 17, 2013
Registry last updated
Oct 31, 2024

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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