Study in Men With Prostate Cancer to Assess the Safety, Pharmacokinetics and Testosterone-Lowering Efficacy of TAK-448

NCT ID: NCT01132404

Last Updated: 2012-01-31

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 9 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-11-30
• Study Completion Date: 2011-12-31

Brief Summary

The phase 1 portion of this study is an open-label, multicenter, dose-escalation study of 1-month depot TAK-448 in adult males with prostate cancer who are either on gonadotropin releasing hormone (GnRH) therapy or who might be eligible for GnRH therapy in the future. The phase 2 portion of this study is an open-label, multicenter, randomized study in men with prostate cancer that will confirm the testosterone- and prostate specific antigen (PSA)- lowering potential of up to 2 dose levels of 1-month depot TAK-448.

Conditions

Prostate Cancer; Prostatic Neoplasms

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

TAK-448 Dose 1

Group Type: EXPERIMENTAL

TAK-448

Intervention Type: DRUG

Phase 1 portion of study:

Patients will be administered a single dose of depot formulation TAK-448 via subcutaneous abdominal injection and a single dose of placebo at a contralateral injection site

Phase 2 portion of the study:

Patients randomized to this arm will be administered depot formulation TAK-448 (up to 2 dose levels) via subcutaneous injection in the abdomen once per month for up to 6 months

TAK-448 Dose 2

Group Type: EXPERIMENTAL

TAK-448

Intervention Type: DRUG

Phase 1 portion of study:

Patients will be administered a single dose of depot formulation TAK-448 via subcutaneous abdominal injection and a single dose of placebo at a contralateral injection site

Phase 2 portion of the study:

Patients randomized to this arm will be administered depot formulation TAK-448 (up to 2 dose levels) via subcutaneous injection in the abdomen once per month for up to 6 months

Leuprorelin

Group Type: ACTIVE_COMPARATOR

Leuprorelin

Intervention Type: DRUG

Phase 2 portion of study: patients randomized to this arm will receive a subcutaneous injection of depot Leuprorelin in the abdomen once per month for up to 6 months

Interventions

Leuprorelin

Phase 2 portion of study: patients randomized to this arm will receive a subcutaneous injection of depot Leuprorelin in the abdomen once per month for up to 6 months

Intervention Type: DRUG

TAK-448

Phase 1 portion of study:

Patients will be administered a single dose of depot formulation TAK-448 via subcutaneous abdominal injection and a single dose of placebo at a contralateral injection site

Phase 2 portion of the study:

Patients randomized to this arm will be administered depot formulation TAK-448 (up to 2 dose levels) via subcutaneous injection in the abdomen once per month for up to 6 months

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male 40 to 72 years of age
• Histologically-confirmed adenocarcinoma of the prostate having completed primary local treatment at least 6 months prior to screening
• Meet all laboratory evaluation values at screening as specified in protocol
• For phase 1 of the study only: Concurrent gonadotropin releasing hormone (GnRH) therapy with generally indolent or stable disease OR a potential candidate of GnRH at some time in the future. Patients with metastatic disease must be asymptomatic with only bone scan positive evidence of metastases. Patients with recurrent local disease will be asymptomatic without bladder, bowel or obstructive symptoms
• For phase 2 portion of the study only: evidence of progressive prostate cancer, which in the opinion of the referring physician and/or study investigator warrants the initiation of GnRH analog therapy. Such patients may have either elevated or rising PSA at least 6 months following primary local therapy (ies) or have evidence of metastatic disease not previously treated with GnRH analog therapy.
• Provision of informed consent and for the phase 1 portion of the study only, willing to participate with no expectation of therapeutic benefit
• Generally fit medical condition, with no acute or chronic medical conditions other than prostate cancer, affecting 2-year life expectancy
• Ability to understand and comply with protocol requirements
• Agreement to, even if surgically sterilized but not surgically castrated, practice effective barrier contraception OR abstain from heterosexual intercourse
• Suitable venous access for blood sampling

Exclusion Criteria

• Advanced or symptomatic metastatic prostate cancer requiring immediate GnRH or additional hormone therapy or requiring chemotherapy
• History of surgical castration
• History of nonskin cancer, other than prostate cancer, requiring active treatment within 2 years of screening
• History of cardiac surgery, within the previous 6 months or any planned elective surgeries, other than skin surgery, during the ensuing 6 months
• Compromise of bone marrow function that would reduce tolerance to repeated blood draws
• History of osteoporosis, unless actively controlled with treatment, or history of vertebral or femoral fracture within the past year
• History of seizures or currently on anticonvulsant medications
• History of major psychiatric illness (diagnosed psychosis or psychiatric illness requiring hospitalization)
• History of drug or significant alcohol abuse
• Participation in clinical trials or receipt of experimental therapy within 2 months of screening
• Serious infection within 14 days before first dose of study drug
• Known history of human immunodeficiency (HIV) infection, hepatitis B, or hepatitis C infection
• History of significant cardiovascular condition

• Participation in the phase 1 portion of the study
• Prior or current use of a GnRH analog or androgen receptor antagonist as first-line hormone therapy (other than as neoadjuvant/adjuvant use)
• History of use of GnRH analog or antagonist (as adjuvant or neoadjuvant therapy) within the 6 months prior to screening
• History of known or documented primary failure of GnRH analog therapy
• History of rising PSA or disease progression while on a GnRH analog or combined androgen blockade (CAB) therapy

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 72 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Millennium Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Monitor

Role: STUDY_DIRECTOR

Millennium Pharmaceuticals, Inc.

Locations

Hôpital Edouard Herriot, 5, Place d'Arsonval, Pavillon V - Urologie et chirurgie de la transplantation

Lyon, , France

Countries

France

Other Identifiers

2009-017668-18

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

C18002

Identifier Type: -

Identifier Source: org_study_id