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

8 marzo 2018 aggiornato da: INSYS Therapeutics Inc

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

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)

Panoramica dello studio

Stato

Ritirato

Tipo di studio

Interventistico

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • District of Columbia
      • Washington, District of Columbia, Stati Uniti, 20007
        • Georgetown University Medical Center
    • Oregon
      • Portland, Oregon, Stati Uniti, 97213-2933
        • Providence Portland Medical Center

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Maschio

Descrizione

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).

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Liposome Entrapped Docetaxel (LE-DT)
Disease status and tumor responses/progression is assessed in accordance to the RECIST guideline
110 mg/m2 IV (in vein) on day 1 of each 21 day cycle, 6 cycles or until disease progression or unacceptable toxicity
Altri nomi:
  • LE-DT
  • Docetaxel liposomiale

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Assessment of serum PSA
Lasso di tempo: 1 year
Measure serum PSA after 2, 4 and 6 cycles of treatment
1 year

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
RECIST method assessment
Lasso di tempo: 1 year
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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Nancy A Dawson, M.D., Georgetown University
  • Investigatore principale: Brendan D Curti, M.D., Providence Health & Services

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 giugno 2010

Completamento primario (Anticipato)

1 settembre 2011

Completamento dello studio (Anticipato)

1 settembre 2011

Date di iscrizione allo studio

Primo inviato

19 agosto 2010

Primo inviato che soddisfa i criteri di controllo qualità

23 agosto 2010

Primo Inserito (Stima)

25 agosto 2010

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 marzo 2018

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 marzo 2018

Ultimo verificato

1 marzo 2018

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Cancro alla prostata

Prove cliniche su Liposome Entrapped Docetaxel (LE-DT)

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