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

NCT01188408 | Withdrawn Phase 2 DMC

• 1 other identifier: LE-DT 201
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 2

Brief 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. 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. 2.To evaluate the measurable soft tissue disease response using the response evaluation criteria in solid tumor (RECIST) methodology
3. 3.To evaluate the progression-free survival (PFS) and overall survival (OS)
4. 4.To correlate PSA expression with tumor response
5. 5.To evaluate the safety of LE-DT at 110 mg/m2 level, in particular peripheral neuropathy, water retention as well as myelotoxicity
6. 6.To evaluate the quality of life (QOL)

Conditions

Prostate Cancer

Outcome Measures

Primary Outcomes (1)

• Assessment of serum PSA

  Measure serum PSA after 2, 4 and 6 cycles of treatment

  1 year

Secondary Outcomes (1)

• RECIST method assessment

  1 year

Study Arms (1)

Liposome Entrapped Docetaxel (LE-DT)

EXPERIMENTAL

Disease status and tumor responses/progression is assessed in accordance to the RECIST guideline

Drug: Liposome Entrapped Docetaxel (LE-DT)

Interventions

Liposome Entrapped Docetaxel (LE-DT) DRUG

110 mg/m2 IV (in vein) on day 1 of each 21 day cycle, 6 cycles or until disease progression or unacceptable toxicity

Also known as: LE-DT, Liposomal Docetaxel

Liposome Entrapped Docetaxel (LE-DT)

Eligibility Criteria

• Age: 18 Years+
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Be 18 years or older and male.
• Have histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate.
• Patients without evidence of PSA progression must have clinical or radiographic evidence of metastatic disease.
• 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.
• 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.
• For patients on an antiandrogen (flutamide, nilutamide, bicalutamide)
• 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.
• 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.
• Chemotherapy-naïve patients (unlimited prior regimens of hormonal therapy are acceptable).
• Have no other malignancy within the past five years, except non-melanoma, skin cancer.
• Have recovered from acute toxicities of prior treatment:
• 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).
• Greater than or equal to 4 weeks must have elapsed since receiving any radiotherapy
• Greater than or equal to 2 weeks must have elapsed since any prior surgery or granulocyte-stimulating growth factor therapy.
• Have the following hematology levels at Baseline:

You may not qualify if:

• Patient has radiographic evidence of active (symptomatic, untreated) intraparenchymal brain metastases; any meningeal metastases; or asymptomatic untreated intraparenchymal brain metastases requiring treatment.
• Patient has received prior chemotherapy for metastatic prostate cancer.
• Patient has a known infection with human immunodeficiency virus or active viral hepatitis.
• Patient has active heart disease including myocardial infarction or congestive heart failure within the previous 6 months, symptomatic coronary artery disease, or uncontrolled arrhythmias.
• 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).
• Any active infection requiring parenteral or oral antibiotics.
• Patient treated with any of the following:
• Taxol, Taxotere or Abraxane for prostate cancer or any prior malignancy
• Concurrent radiation therapy (except for palliative radiotherapy for symptomatic bone metastasis which can be administered as clinically indicated)
• 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).

Sponsors & Collaborators

• INSYS Therapeutics Inc: lead

Study Sites (2)

Georgetown University Medical center

Washington D.C., District of Columbia, 20007, United States

Location

Providence Portland Medical center

Portland, Oregon, 97213-2933, United States

Location

MeSH Terms

Conditions

Prostatic Neoplasms

Condition Hierarchy (Ancestors)

Genital Neoplasms, Male; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Genital Diseases, Male; Genital Diseases; Urogenital Diseases; Prostatic Diseases; Male Urogenital Diseases

Study Officials

• Nancy A Dawson, M.D.

  Georgetown University

  PRINCIPAL INVESTIGATOR

• Brendan D Curti, M.D.

  Providence Health & Services

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: August 19, 2010
• First Posted: August 25, 2010
• Study Start: June 1, 2010
• Primary Completion: September 1, 2011
• Study Completion: September 1, 2011
• Last Updated: March 12, 2018

Record last verified: 2018-03

Locations

US (2)