Efficacy and Safety Study of a New Leuprolide Acetate 17 mg Depot to Treat Prostate Cancer Patients
This study has been terminated.
Sponsor:
GP-Pharm
Information provided by:
GP-Pharm
ClinicalTrials.gov Identifier:
NCT00630799
First received: February 27, 2008
Last updated: September 7, 2010
Last verified: September 2010
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Purpose
This is a multi-center, open-label study of 2 doses of leuprolide acetate 17 mg depot, administered three months apart, in subjects with prostate cancer who might benefit from medical androgen deprivation therapy
| Condition | Intervention | Phase |
|---|---|---|
|
Prostate Cancer |
Drug: leuprolide acetate |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Supportive Care |
| Official Title: | Efficacy and Safety of a New Leuprolide Acetate 17 mg Depot Formulation, GP-Pharm S.A., When Given as Palliative Treatment to Prostate Cancer Patients |
Resource links provided by NLM:
Further study details as provided by GP-Pharm:
Primary Outcome Measures:
- Percent of successful patients achieving chemical castration [ Time Frame: Days 28, 84, and 168 ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- WHO/ECOG performance status [ Time Frame: Days 14, 28, 56, 84, 112, and 168 ] [ Designated as safety issue: No ]
- Serum LH concentration (mIU/mL) [ Time Frame: Days 2, 14, 28, 56, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Serum FSH concentration (mIU/mL) [ Time Frame: Days 2, 14, 28, 56, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Serum PSA concentration (ng/mL) [ Time Frame: Days 2, 14, 28, 56, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Frequency of bone pain [ Time Frame: Days 2, 14, 28, 56, 54, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- plasma testosterone concentration (ng/mL) in PK population [ Time Frame: week 4 and week 12 ] [ Designated as safety issue: No ]
- Occurrence of hot flushes [ Time Frame: Days 0, 2, 14, 28, 56, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Plasma leuprolide concentrations (pg/mL) in PK population [ Time Frame: Days 2, 14, 28, 56, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Frequency of urinary symptoms [ Time Frame: Days 2, 14, 28, 56, 54, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
- Frequency of urinary pain [ Time Frame: Days 2, 14, 28, 56, 54, 84, 86, 112, and 168 ] [ Designated as safety issue: No ]
| Enrollment: | 20 |
| Study Start Date: | May 2008 |
| Study Completion Date: | July 2009 |
| Primary Completion Date: | April 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
leuprolide acetate administered by i.m. injection as two doses of 17 mg each during a period of 6 months (one dose every 3 months)
|
Drug: leuprolide acetate
17 mg i.m.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Males 18 years of age, with histologically proven carcinoma of prostate, who might benefit from medical androgen deprivation therapy;
- life expectancy of at least 1 year;
- WHO/ECOG performance status of 0, 1, or 2;
- adequate renal function at screening as defined by serum creatinine <= 1.6 times the upper limit of normal (ULN) for the clinical laboratory;
- adequate and stable hepatic function as defined by bilirubin <= 1.5 times the ULN and transaminases (i.e. SGOT, SGPT) <= 2.5 times the ULN for the clinical laboratory at screening;
- ability to comprehend the full nature and purpose of the study, including possible risks and side effects; ability to co-operate with the Investigator and to comply with the requirements of the entire study;
- signed written informed consent prior to inclusion in the study.
Exclusion Criteria:
- Evidence of brain metastases, in the opinion of the Investigator, taking into account medical history, clinical observations and symptoms;
- evidence of spinal cord compression, in the opinion of the Investigator, taking into account medical history, clinical observations and symptoms;
- evidence of severe urinary tract obstruction with threatening urinary retention, in the opinion of the Investigator, taking into account medical history, clinical observations and symptoms;
- presence of any tumor in the immediate vicinity which could cause cord compression, in the opinion of the Investigator, taking into account medical history and clinical observations;
- excruciating, severe pain from extensive osseous deposits, in the opinion of the Investigator, taking into account medical history, clinical observations and symptoms;
- testosterone levels <= 1.5 ng/mL at screening, locally determined at the laboratory of each clinical site;
- previous cancer systemic therapy such as chemotherapy, immunotherapy (e.g. antibody therapies, tumor-vaccines), biological response modifiers (e.g. cytokines) within 3 months of baseline;
- previous hormonal therapy for treatment of prostate cancer, such as LHRH analogues (e.g. Lupron®, Zoladex®, etc.) (no wash-out allowed);
- previous treatment with AR-receptor blockers, such as Casodex®, Fugerel®, Megace®, Androcur®(no wash-out allowed);
- previous orchiectomy, adrenalectomy or hypophysectomy;
- previous prostatic surgery (e.g. radical prostatectomy, transurethral resection of the prostate (TUR-P) within 2 weeks prior to or after baseline;
- previous local therapy to the primary tumor with a curative attempt other than surgery (external beam radiotherapy, brachytherapy, thermotherapy, cryotherapy) within 2 weeks prior to or after baseline;
- any investigational drug within 5 half-lives of its physiological action or 3 months, whichever is longer, before baseline;
- administration of 5-α-reductase inhibitors (Proscar®, Avodart®, Propecia®) within 3 months before baseline;
- over-the-counter (OTC) or alternative medical therapies which have an estrogenic or anti-androgenic effect (i.e., PC-SPES, saw palmetto, Glycyrrhiza®, Urinozinc®, DHEA) within the 3 months before baseline;
- hematological parameters (RBC, total and differential WBC count, platelet count, hemoglobin, hematocrit) outside 20% of the upper or lower limits of normal (ULN, LLN) for the clinical laboratory at screening;
- co-existent malignancy, according to the Investigator's opinion;
- uncontrolled congestive heart failure, myocardial infarction or a coronary vascular procedure (e.g. balloon angioplasty, coronary artery bypass graft) or significant symptomatic cardiovascular disease(s) within 6 months before baseline; resting uncontrolled hypertension: >=160/100 mmHg) or symptomatic hypotension within 3 months before baseline;
- venous thrombosis within 6 months of baseline;
- uncontrolled diabetes (patients with uncontrolled diabetes need to compensate the metabolic disorder before treatment with LH-RH analogues);
- history of drug and/or alcohol abuse within 6 months of baseline;
- serious concomitant illness(es) or disease(s) (e.g., hematological, renal, hepatic, respiratory, endocrine, psychiatric) that may interfere with, or put patients at additional risk for, their ability to receive the treatment outlined in the protocol;
- patients on anticoagulative therapy including warfarin (Coumadin®) and heparin. Those patients on low dose low molecular weight heparin may be enrolled in the study;
- Abnormal coagulation studies (PT/PTT) at baseline.
- blood donations/losses within 2 months of baseline, apart from previous prostatic surgery patients (see exclusion 10);
- known hypersensitivity to GnRH, GnRH agonist, including any LHRH analogues, or any excipients of the study formulation;
history of the following prior to the study:
- immunization (within 4 weeks of baseline);
- flu shots (within 1 week of baseline or 1 week prior to and after study drug administration);
- anaphylaxis;
- skin disease which would interfere with injection site evaluation;
- dermatographism will be documented at screening and followed up while on treatment.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00630799
Locations
| United States, Florida | |
| Advanced Research Institute | |
| New Port Richey, Florida, United States, 34655 | |
| United States, New Jersey | |
| Lawrenceville Urology | |
| Lawrenceville, New Jersey, United States, 08648 | |
| United States, New York | |
| Hudson Valley Urology | |
| Poughkeepsie, New York, United States, 12601 | |
| United States, North Carolina | |
| Piedmont Medical Research | |
| Winston-Salem, North Carolina, United States, 27103 | |
| United States, Pennsylvania | |
| Center for Urologic Care | |
| Bryn Mawr, Pennsylvania, United States, 19010 | |
| United States, South Carolina | |
| Carolina Urologic Research Center | |
| Myrtle Beach, South Carolina, United States, 29572 | |
| United States, Tennessee | |
| Urology Associates | |
| Nashville, Tennessee, United States, 37209 | |
| United States, Texas | |
| Urology San Antonio Research, PA | |
| San Antonio, Texas, United States, 78229 | |
Sponsors and Collaborators
GP-Pharm
More Information
No publications provided
| Responsible Party: | Claudio Savulsky/Director, Global Medical Affairs, GP Pharm S.A. |
| ClinicalTrials.gov Identifier: | NCT00630799 History of Changes |
| Other Study ID Numbers: | GP/C/04/PRO |
| Study First Received: | February 27, 2008 |
| Last Updated: | September 7, 2010 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by GP-Pharm:
|
prostate cancer |
Additional relevant MeSH terms:
|
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site Neoplasms Genital Diseases, Male Prostatic Diseases Leuprolide |
Antineoplastic Agents, Hormonal Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Fertility Agents, Female Fertility Agents Reproductive Control Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 16, 2013