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CP-675,206 With Neoadjuvant Hormone Therapy in Patients With High Risk Prostate Cancer

Primary Purpose

Prostatic Neoplasms

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
CP-675,206 and leuprolide acetate and bicalutamide
leuprolide acetate and bicalutamide
Sponsored by
AstraZeneca
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostatic Neoplasms

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: Histologically confirmed adenocarcinoma of the prostate, previously untreated Potential candidate for radical prostatectomy on the basis of the patient's general medical condition, performance status, and life expectancy Potential candidate for NHT prior to prostatectomy, including high or intermediate risk of recurrence, based on an estimated risk of biochemical recurrence: High risk category: PSA >20 or Gleason score 8 or cT2c/cT3 OR Intermediate risk category: PSA >10 and d20 or Gleason score 7 or cT2b No evidence of metastatic disease by physical examination, bone scan, and computed tomography, or MRI, of the abdomen and pelvis Age > 18 years ECOG performance status 0-1 Adequate bone marrow, hepatic, and renal function determined within 2 weeks prior to starting therapy Availability of prostatectomy specimen for histological analysis at the Armed Forces Institute of Pathology Exclusion Criteria: Prior hormone therapy, radiation, chemotherapy, or immunologic therapy for prostate cancer History of, or significant risk for, chronic inflammatory or autoimmune disease Potential requirement for systemic corticosteroids before surgery based on prior history History of autoimmune colitis or chronic GI conditions associated with diarrhea or bleeding, or current acute colitis of any origin Any serious uncontrolled medical disorder or active infection which would impair ability to receive study treatment and subsequent prostatectomy Coexisting malignancies except basal or squamous cell carcinoma of the skin

Sites / Locations

  • Research Site
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Outcomes

Primary Outcome Measures

Assess safety of combination therapy and effectiveness as assessed by pathological response after 3 months of treatment follow for disease status for a maximum of 24 months

Secondary Outcome Measures

assess Pk during treatment monitor for human anti-human antibodies at the end of the study explore genetic influences on safety and/or immune response

Full Information

First Posted
January 5, 2004
Last Updated
June 5, 2012
Sponsor
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT00075192
Brief Title
CP-675,206 With Neoadjuvant Hormone Therapy in Patients With High Risk Prostate Cancer
Official Title
A Phase 1, Open Label, Non-Randomized, Dose Escalation Study to Evaluate the Safety of CP-675,206 in Combination With Neoadjuvant Androgen Ablation and a Phase 2, Open Label, Randomized Study to Evaluate the Efficacy of CP-675,206 in Combination With Neoadjuvant Androgen Ablation and Androgen Ablation Alone in Patients With High Risk Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca

4. Oversight

5. Study Description

Brief Summary
This is a multi-center, open label, randomized study. Patients will be randomized to one of the following arms with an allocation ratio of 3:1, respectively: Arm A: CP-675,206 + neoadjuvant hormone therapy (NHT) OR Arm B: neoadjuvant hormone therapy. After randomization, patients will receive study treatment for three cycles (one cycle is defined as 28 days). After completion of three cycles, patients will undergo a prostatectomy and pathology assessments will be completed at a central laboratory, the Armed Forces Institute of Pathology (AFIP) in Washington, DC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
CP-675,206 and leuprolide acetate and bicalutamide
Intervention Type
Drug
Intervention Name(s)
leuprolide acetate and bicalutamide
Primary Outcome Measure Information:
Title
Assess safety of combination therapy and effectiveness as assessed by pathological response after 3 months of treatment follow for disease status for a maximum of 24 months
Secondary Outcome Measure Information:
Title
assess Pk during treatment monitor for human anti-human antibodies at the end of the study explore genetic influences on safety and/or immune response

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed adenocarcinoma of the prostate, previously untreated Potential candidate for radical prostatectomy on the basis of the patient's general medical condition, performance status, and life expectancy Potential candidate for NHT prior to prostatectomy, including high or intermediate risk of recurrence, based on an estimated risk of biochemical recurrence: High risk category: PSA >20 or Gleason score 8 or cT2c/cT3 OR Intermediate risk category: PSA >10 and d20 or Gleason score 7 or cT2b No evidence of metastatic disease by physical examination, bone scan, and computed tomography, or MRI, of the abdomen and pelvis Age > 18 years ECOG performance status 0-1 Adequate bone marrow, hepatic, and renal function determined within 2 weeks prior to starting therapy Availability of prostatectomy specimen for histological analysis at the Armed Forces Institute of Pathology Exclusion Criteria: Prior hormone therapy, radiation, chemotherapy, or immunologic therapy for prostate cancer History of, or significant risk for, chronic inflammatory or autoimmune disease Potential requirement for systemic corticosteroids before surgery based on prior history History of autoimmune colitis or chronic GI conditions associated with diarrhea or bleeding, or current acute colitis of any origin Any serious uncontrolled medical disorder or active infection which would impair ability to receive study treatment and subsequent prostatectomy Coexisting malignancies except basal or squamous cell carcinoma of the skin
Facility Information:
Facility Name
Research Site
City
La Masa
State/Province
California
ZIP/Postal Code
91442
Country
United States
Facility Name
Research Site
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20307
Country
United States
Facility Name
Research Site
City
Gallatin
State/Province
Tennessee
ZIP/Postal Code
37066
Country
United States
Facility Name
Research Site
City
Hermitage
State/Province
Tennessee
ZIP/Postal Code
37076
Country
United States
Facility Name
Research Site
City
Lebanon
State/Province
Tennessee
ZIP/Postal Code
37087
Country
United States
Facility Name
Research Site
City
Murfreesboro
State/Province
Tennessee
ZIP/Postal Code
37130
Country
United States
Facility Name
Research Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37203
Country
United States
Facility Name
Research Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37205
Country
United States
Facility Name
Research Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37207
Country
United States
Facility Name
Research Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37211
Country
United States
Facility Name
Research Site
City
Smyrna
State/Province
Tennessee
ZIP/Postal Code
37167
Country
United States

12. IPD Sharing Statement

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CP-675,206 With Neoadjuvant Hormone Therapy in Patients With High Risk Prostate Cancer

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