A Study to Monitor the Safety of Enzalutamide in Patients With Progressive Castration-Resistant Prostate Cancer Previously Treated With Docetaxel-Based Chemotherapy

NCT ID: NCT02124668

Last Updated: 2024-11-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-09-23
• Study Completion Date: 2017-05-25

Brief Summary

The purpose of this study is to monitor the safety of enzalutamide in patients with progressive castration-resistant prostate cancer previously treated with docetaxel-based chemotherapy.

Conditions

Castration-Resistant Prostate Cancer; Prostate Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Enzalutamide

Enzalutamide

Group Type: EXPERIMENTAL

Enzalutamide

Intervention Type: DRUG

oral

Interventions

Enzalutamide

oral

Intervention Type: DRUG

Other Intervention Names

Xtandi; MDV3100

Eligibility Criteria

Inclusion Criteria

• Subject has histologically or cytologically confirmed adenocarcinoma of the prostate
• Subject has ongoing androgen deprivation therapy with a gonadotropin-releasing hormone (GnRH) analogue (agonist or antagonist) and plans to maintain throughout the study period or has had a prior orchiectomy (i.e., surgical or medical castration)
• Subject has had at least one prior chemotherapy regimen for metastatic castration-resistant prostate cancer with at least one regimen containing docetaxel
• Subject has progressive disease and indication for change of antineoplastic regimen
• Subject has no known or suspected brain metastasis
• Subject has an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
• Subject is able to swallow the study drug and comply with study requirements
• There is no comparable or satisfactory alternative therapy to treat the subject's disease
• Subject agrees not to participate in another interventional study while on treatment

Exclusion Criteria

• Subject has severe concurrent disease, infection, or co-morbidity that would make the subject inappropriate for enrollment
• Subject's absolute neutrophil count is < 1000/μL, or platelet count < 100,000/μL, or hemoglobin < 6.2 mmol/L (or < 10 g/dL)
• Subject's total bilirubin is ≥ 1.5 x upper limit of normal (ULN) (except for subjects with documented Gilbert's disease) or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) is ≥ 2.5x ULN
• Subject's estimated creatinine clearance is less than 30 mL/min by the Cockcroft and Gault formula
• Subject has albumin ≤ 30 g/L (or ≤ 3.0 g/dL)
• Subject has received anti-androgen therapy (e.g. bicalutamide), chemotherapy, or biologic therapy for prostate cancer (other than bone targeted agents such as bisphosphonates or denosumab, gonadotropin-releasing hormone (GnRH) analogue therapy, or glucocorticoids which are allowed) within 4 weeks of Day 1
• Subject has had prior use of abiraterone
• Subject has prior use, or participation in a clinical trial, of an investigational agent that blocks androgen synthesis (e.g. TAK-700) or targets the androgen receptor (e.g. ARN-509, ODM-201)
• Subject has:

1. A history of seizure, including any febrile seizure or any condition that may predispose to seizure including, but not limited to underlying brain injury, stroke, primary brain tumors, brain metastases,

2. A history of loss of consciousness or transient ischemic attack within 12 months of Screening

• Subject has clinical signs suggestive of high or imminent risks for pathological fracture, spinal cord compression and/or cauda equina syndrome
• Subject has a significant cardiovascular disease
• Subject has received investigational therapy within 28 days or 5 half lives, whichever is longer, prior to Screening
• Subject has undergone major surgery within 4 weeks prior to Screening
• Subject has shown a hypersensitivity reaction to the active pharmaceutical ingredient or any of the capsule components, including Labrasol, butylated hydroxyanisole, and butylated hydroxytoluene
• Subject has used or plans to use, from 30 days prior to enrollment through the end of the study, medications known to lower the seizure threshold or prolong the QT interval

• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Medivation LLC, a wholly owned subsidiary of Pfizer Inc.

INDUSTRY

Sponsor Role: collaborator

Astellas Pharma Europe B.V.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Astellas Pharma Europe B.V.

Locations

Site GE99503

Tbilisi, , Georgia

Site GE99502

Tbilisi, , Georgia

Site RU70002

Moscow, , Russia

Site RU70003

Moscow, , Russia

Countries

Georgia; Russia

Related Links

https://astellasclinicalstudyresults.com/study.aspx?ID=250

Link to results on the Astellas Clinical Study Results website

Other Identifiers

9785-CL-0122

Identifier Type: -

Identifier Source: org_study_id