Overview

A Positron Emission Tomography/Computed Tomography (PET/CT) Bone Imaging Study in Patients Receiving Enzalutamide for Castration-Resistant Prostate Cancer (CRPC)

Status:
Completed
Trial end date:
2019-05-03
Target enrollment:
0
Participant gender:
Male
Summary
The purpose of this study is to evaluate 18F-sodium fluoride positron-emission tomography / computed tomography (18F-NaF PET/CT) imaging as a method for determining treatment response in metastatic bone lesions in patients who are receiving enzalutamide for castration-resistant prostate cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Medivation, Inc.
Pfizer
Collaborators:
Astellas Pharma Inc
Medivation LLC, a wholly owned subsidiary of Pfizer Inc.
Criteria
Inclusion Criteria:

- Histologically or cytologically confirmed adenocarcinoma of the prostate without
neuroendocrine differentiation, or signet cell or small cell features;

- Presence of bone metastatic disease as assessed by at least two lesions on whole body
metastable technetium-methylene diphosphonate (99mTc-MDP) bone scintigraphy;

- Throughout the study, ongoing androgen deprivation therapy with a luteinizing
hormone-releasing hormone (LHRH) analogue or prior bilateral orchiectomy (medical or
surgical castration);

- Testosterone ≤ 1.73 nmol/L (≤ 50 ng/dL) at screening;

- Progressive disease on androgen deprivation therapy at screening defined as a minimum
of two sequentially rising prostate-specific antigen (PSA) values (PSA1 < PSA2 <
PSA3);

- The screening PSA (PSA3) must be ≥ 2 μg/L (≥ 2 ng/mL).

Exclusion Criteria:

- Prior enzalutamide, abiraterone acetate, aminoglutethimide, ketoconazole, radium Ra
223 dichloride or other bone-targeting radionuclides, or cytotoxic chemotherapy in the
CRPC setting for the treatment of prostate cancer or participation in a clinical trial
of an investigational agent that inhibits the androgen receptor or androgen synthesis
(unless treatment was placebo);

- Treatment with hormonal therapy (eg, androgen receptor inhibitors, 5-alpha reductase
inhibitors) or biologic therapy for prostate cancer (other than LHRH analogue therapy)
within 4 weeks before enrollment;

- Initiation of new treatment with denosumab, bisphosphonates, or systemic
corticosteroids for treatment of prostate cancer within 4 weeks before enrollment;

- Use of an investigational agent within 4 weeks before the screening visit;

- Radiation therapy to bone within 4 weeks before enrollment;

- Use of opiate analgesics for prostate cancer pain within 4 weeks before enrollment;

- Screening 99mTc-MDP bone scintigraphy showing a superscan;

- Visceral (eg, lung, liver) metastatic disease. Adenopathy is allowed;

- Current or previously treated brain metastasis or active leptomeningeal disease;

- History of seizure any time in the past for any reason or any condition that may
predispose to seizures.