Efficacy and Safety of Leuprolide Acetate 22.5 mg Depot in Treatment of Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

Efficacy and Safety of a New Leuprolide Acetate 22.5 mg Depot Formulation in the Treatment of Prostate Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01415960
• Other study ID #: GP/C/05/PRO
• Status: Active, not recruiting
• Phase: Phase 3
• First received: August 11, 2011
• Last updated: August 26, 2013
• Start date: September 2011
• Est. completion date: August 2013

Study information

• Verified date: August 2013
• Source: GP-Pharm
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Some patients with prostate cancer benefit from androgen deprivation therapy which reduces levels of testosterone. Leuprolide is a synthetic Luteinizing hormone releasing hormone (LHRH) analogue which upon administration can decrease testosterone levels to ≤0.5 ng/mL. Leuprolide Acetate 22.5 mg Depot is a microencapsulated formulation of leuprolide which is released slowly over time and effectively reduces testosterone levels in many patients to ≤0.5 ng/mL for up to three months. In this study Leuprolide acetate 22.5 mg Depot will be administered by intramuscular injection twice over a period of 6 months. The proportion of patients with testosterone ≤0.5 ng/mL evaluated over a period of 168 days.

Description:

This in an open-label, multicenter, multiple-dose investigation of 2 doses of leuprolide acetate 22.5 mg administered with a 3-month interval to patients with histologically proven carcinoma of prostate who might benefit from medical androgen deprivation therapy. A total of up to 160 male patients will receive their first single intramuscular injection of leuprolide acetate 22.5 mg on Day 0 (after baseline assessment) and then after 3 months (Day 84). The study duration will be 6 months. Thirty(30) patients will be screened per protocol and enrolled at selected centers to form the PK cohort. The PK/PD analysis will be performed using plasma specimens from the first 20 of 30 patients enrolled in the study (and included in the PK/PD cohort). Patients not belonging to the PK cohort will be screened and enrolled per protocol and will follow the same study schedule as those enrolled in the PK portion of the study, except they will provide only sparse PK sampling.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 160
• Est. completion date: August 2013
• Est. primary completion date: May 2013
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Main selection criteria:

Patients with histologically documented prostate cancer who might benefit from medical androgen deprivation therapy (i.e., reduction of androgen levels) will be considered for enrollment in the study if they meet the following criteria:

Inclusion Criteria:

1. Males =18 years of age

2. Patients with histologically documented prostate carcinoma who might benefit from medical androgen deprivation therapy.

3. Life expectancy of at least 1 year.

4. WHO/ECOG performance status of 0, 1, or 2.

5. Adequate renal function at Screening as defined by serum creatinine =1.6 times the upper limit of normal (ULN) for the clinical laboratory.

6. Adequate and stable hepatic function as defined by bilirubin =1.5 times the ULN and transaminases (i.e., aspartate aminotransferase, alanine aminotransferase) =2.5 times the ULN for the clinical laboratory at Screening.

7. Ability to comprehend the full nature and purpose of the study, including possible risks and side effects; ability to cooperate with the investigator and to comply with the requirements of the entire study.

8. Following receipt of verbal and written information about the study,the patient must provide signed informed consent before any study related activity is carried out.

Exclusion Criteria:

1. Evidence of brain metastases, in the opinion of the investigator, taking into account medical history, clinical observations, and symptoms (rationale: to minimize possibility of serious acute flare reactions that would necessitate concomitant administration of other drugs).

2. Evidence of spinal cord compression, in the opinion of the investigator, taking into account medical history, clinical observations, and symptoms (rationale: see rationale in criterion 1).

3. 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 (rationale: see rationale in criterion 1).

4. Presence of any tumor in the immediate vicinity that could cause spinal cord compression, in the opinion of the investigator, taking into account medical history and clinical observations (rationale: see rationale in criterion 1).

5. Excruciating, severe pain from extensive osseous deposits, taking into account medical history, clinical observations, and symptoms (rationale: see rationale in criterion 1).

6. Testosterone levels <1.5 ng/mL at Screening, This testosterone level will be locally determined at the laboratory of each clinical site (rationale: to ensure that all patients have normal baseline testosterone levels).

7. Previous androgen ablative therapy lasting more than 6 months, such as LHRH analogues (e.g., Leuprolide acetate, Goserelin, Buserelin) or antagonists (degarelix). Also, therapy must have not occurred within 12 months before the screening visit. Any prior ADT must have not exceeded 6 months of therapy.

8. Previous treatment with androgen-receptor blockers, such as Bicalutamide, Flutamide, Megestrol acetate, Ciproterone will only be allowed after a 3 month washout prior to the screening visit (rationale: these therapies alter a patient's androgenic hormonal response for a sustained period).

9. Previous orchiectomy, adrenalectomy, or hypophysectomy (no washout allowed) (rationale: these therapies could have altered a patient's androgenic hormonal response).

10. Previous prostatic surgery (e.g., radical prostatectomy, transurethral resection of the prostate) within 2 weeks before Baseline (rationale: these therapies could have altered a patient's androgenic hormonal response and/or adverse reaction profile).

11. Previous local therapy to the primary tumor with a curative attempt other than surgery (external beam radiotherapy, brachytherapy, thermotherapy, cryotherapy) within 2 weeks before Baseline (rationale: these therapies could have altered a patient's adverse reaction profile).

12. Previous cancer systemic therapy such as chemotherapy, immunotherapy (e.g., antibody therapies, tumor vaccines), biological response modifiers (e.g., cytokines).

13. Any investigational drug within 5 half-lives of its physiological action or 3 months, whichever is longer, before Baseline (rationale: to prevent adverse effects of another drug being attributed to study drug and to prevent potential interactions).

14. Administration of 5-a-reductase inhibitors (Finasteride, Dutasteride) within 3 months before Baseline (rationale: alters PSA levels and androgen metabolism of the prostate cells). Prior use of 5-a-reductase inhibitors will be allowed with a 3 month washout.

15. Over-the-counter or alternative medical therapies that have an estrogenic or antiandrogenic effect (i.e., PC-SPES, saw palmetto, Glycyrrhiza, Urinozinc, dehydroepiandrosterone) within the 3 months before Baseline.

16. Hematological parameters (red blood cells, total and differential white blood cell count, platelet count, hemoglobin, hematocrit) outside 20% of the ULN or lower limits of normal for the clinical laboratory at Screening (rationale: to render potential study drug-related laboratory abnormalities easier to observe).

17. Coexistent malignancy, in the opinion of the investigator (rationale: to decrease possibility of disease-caused or associated therapy-caused adverse effects being attributed to study drug).

18. 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 mm Hg) or symptomatic hypotension within 3 months before Baseline (rationale: to decrease possibility of disease-caused or associated therapy-caused adverse effects being attributed to study drug).

19. Venous thrombosis within 6 months of Baseline (rationale: influencing testosterone levels may be associated with increased likelihood of deep venous thrombosis).

20. Uncontrolled diabetes, in the opinion of the investigator (rationale:

patients with uncontrolled diabetes need to compensate the metabolic disorder before treatment with LHRH analogues).

21. History of drug and/or alcohol abuse within 6 months of Baseline (rationale: these patients are likely to have numerous medical abnormalities and are unlikely to comply with protocol).

22. 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 (rationale: to decrease possibility of disease-caused or associated therapy-caused adverse effects being attributed to study drug).

23. Patients on anticoagulative therapy including warfarin (Coumadin®), Dabigatran Etexilate (Pradaxa®) and heparin. Those patients on low-dose, low-molecular weight heparin may be enrolled in the study (rationale: to decrease possibility of disease-caused or associated therapy-caused adverse effects being attributed to study drug). Plavix and Aspirin are allowed for cardiac prophylaxis as long as all inclusion/exclusion criteria are met concerning coagulation parameters and thromboembolic history. Special care to avoid hematoma at the injection site must be observed.

24. Abnormal coagulation studies (prothrombin time [PT]/partial thromboplastin time [PTT]) at Baseline.

25. History of serious bleeding on injections, an elevated INR, concomitant medications or any other condition (i.e. significant thrombocytopenia) that in opinion of the investigator would render the subject at risk of significant bleeding with injections.

26. Blood donations/losses within 2 months of Baseline, apart from previous prostatic surgery patients (see exclusion 10 [rationale: to avoid excessive blood donations]).

27. Known hypersensitivity to GnRH, GnRH agonists, including any LHRH analogues, or any excipients of the study formulation (rationale: to minimize hypersensitivity reaction to study drug).

28. History of Immunization (within 4 weeks of Baseline) and specifically flu shots (within 1 week of Baseline or 1 week before and after study drug administration) (Rationale: to decrease the possibility of non treatment-related AEs being attributed to study drug).

29. Skin disease that would interfere with injection site evaluation.

30. Men not willing to use appropriate birth control methods such as surgical sterilization or barrier contraception or men with partners of child bearing potential not willing to use appropriate birth control methods, such as surgical sterilization, hormonal birth control (partner), an intrauterine device (partner) or double-barrier method for the entire study period.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• Leuprolide acetate 22.5 mg depot, GP-Pharm SA
Administered by im injection, twice during the study, three months apart

Locations

Country	Name	City	State
United States	The Urological Institute of Northeastern New York	Albany	New York
United States	Urologic Consultants of SE PA	Bala Cynwyd	Pennsylvania
United States	Brooklyn Urology Research Group	Brooklyn	New York
United States	Urology Health Specialists, LLC	Bryn Mawr	Pennsylvania
United States	Seattle Urology Research Center	Burien	Washington
United States	North Idaho Urology	Coeur d'Alene	Idaho
United States	Atlantic Urological Associates	Daytona Beach	Florida
United States	Mid Atlantic Clinical Research	Greenbelt	Maryland
United States	Greenville Health System	Greer	South Carolina
United States	First Urology	Jeffersonville	Indiana
United States	Premier Urology Associates, LLC	Lawrenceville	New Jersey
United States	Idaho Urologic Institute	Meridian	Idaho
United States	Carolina Urologic Research Center	Myrtle Beach	South Carolina
United States	Urology Associates, PC	Nashville	Tennessee
United States	Manhattan Medical Research	New York	New York
United States	Urology Health Team	Ocala	Florida
United States	Winter Park Urology Associates, PA	Orlando	Florida
United States	The Premier Medical Group of the Hudson Valley, PC	Poughkeepsie	New York
United States	Urology San Antonio Research, PA	San Antonio	Texas
United States	Genesis Research	San Diego	California
United States	Coastal Medical Center	Sarasota	Florida
United States	Staten Island Urological Research, PC	Staten Island	New York
United States	Urology of Virginia	Virginia Beach	Virginia
United States	PMG Research of Wilmington	Wilmington	North Carolina
United States	PMG Research of Winston Salem	Winston Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
GP-Pharm

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint is testosterone =0.5 ng/mL assessed at Days 28, 84, and 168.	The primary objective of this study is to determine the proportion of successful patients achieving chemical castration (defined as castrate testosterone levels =0.5 ng/mL) at Days 28, 84, and 168.	168 days	No
Secondary	Determination of serum luteinizing hormone (LH),		168 days	No
Secondary	follicle-stimulating hormone (FSH)		168 days	No
Secondary	prostate-specific antigen (PSA) concentrations		168 days	No
Secondary	Determination of leuprolide Cmax, Tmax, Cwk4, Cwk12, AUC0-t, AUC0-48h, AUC0-4wks, AUC0-12wks, Cavg (0-12wks).		168 days	No
Secondary	Safety endpoints	Safety endpoints adverse events (AEs), local tolerability, vital signs, performance status, bone pain, urinary pain, and urinary symptoms, occurrence of hot flushes and clinical laboratory and electrocardiogram (ECG) results.	168 Days	Yes