A Study of Apalutamide in Participants With High‑Risk, Localized or Locally Advanced Prostate Cancer Who Are Candidates for Radical Prostatectomy
Status: | Not yet recruiting |
---|---|
Conditions: | Prostate Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/10/2019 |
Start Date: | February 28, 2019 |
End Date: | December 28, 2027 |
Contact: | Study Contact |
Email: | JNJ.CT@sylogent.com |
Phone: | 844-434-4210 |
A Randomized, Double-blind, Placebo-controlled, Phase 3 Study of Apalutamide in Subjects With High-risk, Localized or Locally Advanced Prostate Cancer Who Are Candidates for Radical Prostatectomy
The purpose of this study is to determine if treatment with androgen deprivation therapy
(ADT) plus apalutamide (with or without abiraterone acetate with prednisone [AAP]) before and
after radical prostatectomy in participants with high-risk localized or locally advanced
prostate cancer results in an improvement in pathological complete response (pCR) rate and
metastasis-free survival (MFS), as compared to ADT plus placebo.
(ADT) plus apalutamide (with or without abiraterone acetate with prednisone [AAP]) before and
after radical prostatectomy in participants with high-risk localized or locally advanced
prostate cancer results in an improvement in pathological complete response (pCR) rate and
metastasis-free survival (MFS), as compared to ADT plus placebo.
Inclusion Criteria:
- Histologically confirmed adenocarcinoma of the prostate
- Candidate for radical prostatectomy as per the investigator
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1
- Contraceptive (birth control) use by men (or female partners of men enrolled in the
study who are of childbearing potential or are pregnant) should be consistent with
local regulations regarding the acceptable methods of contraception for those
participating in clinical studies
- Able to receive androgen deprivation therapy (ADT) for up to 1 year, per the
investigator's assessment
Exclusion Criteria:
- Distant metastasis (clinical stage M1). Nodal disease below the iliac bifurcation
(clinical stage N1) is not an exclusion. Diagnosis of distant metastasis (clinical M
stage; M0 versus M1a, M1b, M1c) and pelvic nodal disease (clinical N stage; N1 versus
N0) will be assessed by central radiological review. Participants are considered
eligible only if the central radiological review confirms clinical stage M0
- Prior treatment with anti-androgen
- Prior treatment for prostate cancer
- Pathological finding consistent with small cell, ductal or neuroendocrine carcinoma of
the prostat
- History of any pelvic radiation
We found this trial at
33
sites
Orange, California 92868
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Cedars Sinai Med Ctr Cedars-Sinai is known for providing the highest quality patient care. Our...
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University of Southern California The University of Southern California is one of the world’s leading...
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Albany Medical College Albany Medical Center is northeastern New York's only academic health sciences center...
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Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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3855 Health Sciences Dr,
La Jolla, California 92093
La Jolla, California 92093
(858) 822-6100
UC San Diego Moores Cancer Center Established in 1978, UC San Diego Moores Cancer Center...
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823 82nd Parkway, Suite B
Myrtle Beach, South Carolina 29572
Myrtle Beach, South Carolina 29572
(843) 449-1010 ext.268
Carolina Urologic Research Center Carolina Urologic Research Center (CURC) has been recognized both nationally and...
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Florida Hospital Florida Hospital is one of the country
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