Efficacy and Safety Study of LE-DT to Treat Metastatic Castrate Resistant Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

A Multicenter, Open-Label, Phase II Study of LE-DT for Efficacy and Safety in Patients With Metastatic Castrate Resistant Prostate Cancer

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01188408
• Other study ID #: LE-DT 201
• Status: Withdrawn
• Phase: Phase 2
• First received: August 19, 2010
• Last updated: March 8, 2018
• Start date: June 2010
• Est. completion date: September 2011

Study information

• Verified date: March 2018
• Source: INSYS Therapeutics Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

LE-DT is a novel, proprietary delivery system of docetaxel developed by NeoPharm, Inc. Docetaxel (currently marketed as Taxotere) is an anti-microtubular network agent and is one of the most active agents in the treatment of metastatic castrate resistant prostate cancer (CRPC) and other variety of cancers. Taxotere has poor solubility and is designed to be administered with Tween 80 in ethanol. This vehicle causes acute hypersensitivity reaction. By removing toxic detergent used in Taxotere, the form of LE-DT, shows reduced toxicity and comparable therapeutic efficacy in pre-clinical study. The clinical evidence obtained from the NeoPharm Phase I study shows fewer side effects and possibly administered at higher dose to induce greater effectiveness of LE-DT. The current Phase II study is designed to accomplish the following objectives:

1. Assess the antitumor effect indicator serum prostate specific antigen (PSA) following the intravenous (IV) administration of 110 mg/m2 LE-DT every three weeks in patients with metastatic castrate resistant prostate cancer

2. To evaluate the measurable soft tissue disease response using the response evaluation criteria in solid tumor (RECIST) methodology

3. To evaluate the progression-free survival (PFS) and overall survival (OS)

4. To correlate PSA expression with tumor response

5. To evaluate the safety of LE-DT at 110 mg/m2 level, in particular peripheral neuropathy, water retention as well as myelotoxicity

6. To evaluate the quality of life (QOL)

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: September 2011
• Est. primary completion date: September 2011
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Be 18 years or older and male.

2. Have histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate.

3. Patients without evidence of PSA progression must have clinical or radiographic evidence of metastatic disease.

4. Must have castrate levels of testosterone (serum testosterone less than 50ng/dl) by either being on androgen ablation therapy with a luteinizing hormone-releasing hormone (LHRH) agonist or have had a prior bilateral orchiectomy.

5. Patients must have documented evidence of disease progression: progressive disease is defined as a minimum of three consecutive elevations in PSA each obtained a minimum of one week apart with the last value being greater than 2 ng/mL and/or new metastatic lesions on bone scan (minimum of 2) and/or new or progressive disease on CT or MRI scan.

6. For patients on an antiandrogen (flutamide, nilutamide, bicalutamide)

1. If given as part of first line therapy or for patients who did respond to antiandrogen second line therapy, the patient must demonstrate progression of disease at least 4 weeks beyond discontinuation of such agents to rule out an antiandrogen withdrawal response.

2. If given as a second line therapy and the patient did not respond or had a decline in PSA for less than 3 months, it is not required to observe for a withdrawal response.

7. Chemotherapy-naïve patients (unlimited prior regimens of hormonal therapy are acceptable).

8. Have no other malignancy within the past five years, except non-melanoma, skin cancer.

9. Have recovered from acute toxicities of prior treatment:

1. Greater than or equal to 4 weeks must have elapsed since receiving hormonal therapy (except for chronic non-investigational gonadotropin releasing hormone analogs or other primary androgen suppressive therapy which are required), biologic agents or any investigational agent (palliative bisphosphonate therapy for bone pain can be administered as clinically indicated).

2. Greater than or equal to 4 weeks must have elapsed since receiving any radiotherapy

3. Greater than or equal to 2 weeks must have elapsed since any prior surgery or granulocyte-stimulating growth factor therapy.

10. Have the following hematology levels at Baseline:

1. Absolute Neutrophil Count (ANC) greater than or equal to1,500 x 106 cells/L

2. Platelets greater than or equal to 100 x 109 cells/L

3. Hemoglobin greater than or equal to 9 g/L.

11. Have the following chemistry levels at Baseline:

1. AST (SGOT), ALT (SGPT) less than or equal to 1.5 x ULN

2. Total bilirubin less than or equal to 1.5 ULN

3. Creatinine less than or equal to 1.5 ULN; or 24-hour creatinine clearance greater than 60 mL/min

4. Normal serum electrolytes and magnesium levels

12. Have a life expectancy of greater than or equal to 12 weeks.

13. Have an Eastern Cooperative Oncology Group (ECOG) Performance status of 0-2.

14. Patient or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee (EC)/Institutional Review Board (IRB)-approved written informed consent form (ICF) prior to receiving any study related procedure.

Exclusion Criteria:

1. Patient has radiographic evidence of active (symptomatic, untreated) intraparenchymal brain metastases; any meningeal metastases; or asymptomatic untreated intraparenchymal brain metastases requiring treatment.

2. Patient has received prior chemotherapy for metastatic prostate cancer.

3. Patient has a known infection with human immunodeficiency virus or active viral hepatitis.

4. Patient has active heart disease including myocardial infarction or congestive heart failure within the previous 6 months, symptomatic coronary artery disease, or uncontrolled arrhythmias.

5. Any condition which in the Investigator's opinion deems the patient an unsuitable candidate to receive study drug (e.g., uncontrolled bleeding or bleeding diathesis).

6. Any active infection requiring parenteral or oral antibiotics.

7. Patient treated with any of the following:

1. Taxol, Taxotere or Abraxane for prostate cancer or any prior malignancy

2. Concurrent radiation therapy (except for palliative radiotherapy for symptomatic bone metastasis which can be administered as clinically indicated)

8. Patient has pre-existing peripheral neuropathy of Grade greater than 1 based on the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE).

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• Liposome Entrapped Docetaxel (LE-DT)
110 mg/m2 IV (in vein) on day 1 of each 21 day cycle, 6 cycles or until disease progression or unacceptable toxicity

Locations

Country	Name	City	State
United States	Providence Portland Medical center	Portland	Oregon
United States	Georgetown University Medical center	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
INSYS Therapeutics Inc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of serum PSA	Measure serum PSA after 2, 4 and 6 cycles of treatment	1 year
Secondary	RECIST method assessment	Measurable soft tissue disease response based on the RECIST method, PFS, and OS will also be assessed after 2, 4 and 6 cycle to determine the treatment effectiveness with LE-DT after treatment	1 year