Dose-Seeking Trial of PCK3145 in Asymptomatic, Castrate Metastatic Prostate Cancer Patients.

A Phase I Randomized Dose-Seeking Trial of PCK3145 in Asymptomatic, Castrate Metastatic Prostate Cancer Patients.

The purpose of this study is to find out whether giving a drug called PCK3145 can reduce the level of a protein in the blood called MMP-9 as well as to find out how long the drug will remain in your system over time. This drug has been tested previously in prostate cancer patients abroad and has been shown to be safe with minimal side effects. However, we do not know whether changes in MMP-9 levels correlate with tumor shrinkage or symptom improvement. We would also like to evaluate the potential pain relief (analgesic) effect of PCK3145 at 15mg/m² i.v. weekly for 12 weeks on patients with both symptomatic and asymptomatic castrate metastatic prostate cancer who are dependent on opioid analgesics. We would also like to monitor pain through a brief pain questionaire, and determine the impact on markers of bone turnover.

Study Overview

• Status: Completed
• Conditions: Prostate Cancer
• Intervention / Treatment: Drug: PCK3145; Drug: PCK3145

• Study Type: Interventional
• Enrollment (Actual): 36
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • New York
    • New York, New York, United States, 10065
      • Memorial Sloan Kettering Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patients who have castrate metastatic prostate cancers are eligible based on the following criteria.
• Patients with prostate cancer must have castrate metastatic disease (i.e. disease progression following castration or treatment with a gonadotropin releasing hormone analog. Patients with prostate cancer may have progressing metastatic disease on imaging studies (bone scan, CT scan or MRI) in addition to a rising PSA.
• Biochemical progression will be defined as: A minimum of three rising PSA values from a baseline that are obtained 1 week or more apart, or two rising PSA values more than one month apart, where the percentage increase over the range of values is at least 25%.
• Maintaining castrate status: Patients who have not undergone surgical orchiectomy should continue on medical therapies [i.e. gonadotropin releasing hormone analogs] to maintain castrate levels of serum testosterone. Patients who are receiving an anti-androgen as part of first line hormonal therapy must have shown progression of disease off the anti-androgen prior to enrollment.
• Histologically confirmed diagnosis of prostate cancer per MSKCC review.
• No limitations on the duration of or number of prior therapies.
• Age ≥ 18 years
• Karnofsky performance status ≥ 70% (ECOG ≤ 1.0).
• Life expectancy of greater than 6 months.
• Hematologic: WBC ≥ 3000K/μl.
• Absolute neutrophil count ≥ 1500 K/μl
• Platelet count ≥ 100,000 K/μl.
• Hepatic: Total Bilirubin - within normal institutional limits
• AST < 1.5 x ULN, ALT < 1.5 x ULN.
• Renal: Creatinine < 2.0 or creatinine clearance > 55 mL/min
• Coagulation: Prothrombin time - Less than or equal to the ULN (upper limit of normal) unless patient is taking anticoagulants
• Patients must have recovered from the acute toxicities of any prior therapy, and not received chemotherapy, radiation therapy or other investigational anticancer therapeutic drugs for at least 4 weeks prior to entry.
• Ability to understand and the willingness to sign a written informed consent document.
• Testosterone < 50 ng/dl
• Patients may be symptomatic and must be dependent on opioid analgesics or nonsteroidal anti-inflammatory drugs

Exclusion Criteria:

• Patients who have had chemotherapy or radiotherapy within 4 weeks prior to entering the study or those who have not recovered from the adverse events due to agents administered more than 4 weeks earlier.
• Patients may not be receiving any other investigational agents.
• Patients with active brain metastases or epidural disease
• Uncontrolled intercurrent illness including but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• No current therapy with alternative/complementary drugs such as PC Plus, saw palmetto or Zyflamend.
• No rectal bleeding except that seen following radiation proctitis or known history of hemorrhoids.
• Non-prostate primary carcinoma except for non-melanoma skin cancer within previous 5 years.
• No uncontrolled cardiac arrhythmias.
• Patient taking steroids for cord compression or pain control are excluded. Patient on steroids for chronic conditions such as arthritis or asthma or on chronic hydrocortisone post ketoconazole will be permitted.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 1; 15 mg/m2 weekly of PCK3145	Drug: PCK3145; i.v. bolus either 15 mg/m2 weekly of PCK3145.; Drug: PCK3145; by i.v. bolus 7.5 mg/m2 twice per week of PCK3145
Experimental: 2; 7.5 mg/m2 twice per week of PCK3145	Drug: PCK3145; i.v. bolus either 15 mg/m2 weekly of PCK3145.; Drug: PCK3145; by i.v. bolus 7.5 mg/m2 twice per week of PCK3145

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To explore the PK profiles and their association with two dosing schedules of PCK3145 given iv bolus in patients with asymptomatic castrate metastatic prostate cancer.	conclusion of the study

Secondary Outcome Measures

Outcome Measure	Time Frame
To explore the association of 2 dosing schedules of PCK3145 with MMP-9 levels in asymptomatic pts with castrate metastatic prostate cancer. The results of this analysis will be used to establish a dose on which to build a phase II randomized trial.	conclusion of the study
To assess the safety and toxicity of PCK3145 at a dose of 150mg/m² i.v. bolus given weekly for 16 weeks.	conclusion of the study

Collaborators and Investigators

• Sponsor: Memorial Sloan Kettering Cancer Center
• Collaborators: Ambrilia Biopharma, Inc.

Publications and helpful links

Helpful Links

• Memorial Sloan-Kettering Cancer Center

Study record dates

Study Major Dates

• Study Start: March 1, 2005
• Primary Completion (Actual): March 1, 2009
• Study Completion (Actual): March 1, 2009

Study Registration Dates

• First Submitted: June 10, 2008
• First Submitted That Met QC Criteria: June 11, 2008
• First Posted (Estimate): June 12, 2008

Study Record Updates

• Last Update Posted (Estimate): March 30, 2009
• Last Update Submitted That Met QC Criteria: March 27, 2009
• Last Verified: March 1, 2009

More Information

Terms related to this study

• Keywords: Prostate; PCK3145
• Additional Relevant MeSH Terms: Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Genital Neoplasms, Male; Prostatic Diseases; Prostatic Neoplasms
• Other Study ID Numbers: 05-019