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A Study of CriPec® Docetaxel Given to Patients With Solid Tumours (NAPOLY)

21 settembre 2018 aggiornato da: Cristal Therapeutics

A Phase I Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of CriPec® Docetaxel in Patients With Solid Tumours

The goal of this Phase1 clinical research study is to find the highest safe dose of CriPec® docetaxel that can be given in the treatment of patients with solid tumours.

Panoramica dello studio

Stato

Completato

Intervento / Trattamento

Descrizione dettagliata

The study is designed to explore the safety, tolerability, pharmacokinetics and pharmacodynamics of CriPec® docetaxel and to identify the Maximum Tolerated Dose (MTD).

Tipo di studio

Interventistico

Iscrizione (Effettivo)

33

Fase

  • Fase 1

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

      • Leuven, Belgio
        • University Hospital Leuven
      • Amsterdam, Olanda
        • VUMC Amsterdam
      • Groningen, Olanda
        • UMC Groningen
      • Rotterdam, Olanda
        • Erasmus 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

Tutto

Descrizione

Inclusion Criteria:

  1. At least 18 years old
  2. Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1
  3. Estimated life expectancy of at least 12 weeks
  4. Ability and willingness to give written informed consent and to comply with the requirements of the study

    For Part 1:

  5. Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive solid tumours that are refractory to standard therapy or for whom no standard therapy exists and with measurable or evaluable disease according to RECIST 1.1.

    For Part 2:

  6. Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive cancer with measurable disease according to RECIST 1.1 of a histological type that are refractory to standard therapy or for whom no standard therapy exists and where treatment with a taxane is an appropriate treatment option.

Exclusion Criteria:

  1. Less than 4 weeks since the last treatment of chemotherapy, biological therapy, immunotherapy or systemic radiotherapy (except palliative radiation delivered to <20% of bone marrow), and less than 6 weeks for nitrosoureas and mitomycin C prior to Cycle 1 Day 1.
  2. Current or recent (within 4 weeks prior to Cycle 1 Day 1) treatment with another Investigational Product or participation in another investigational interventional study.
  3. Symptomatic brain metastases.
  4. Toxicities incurred as a result of previous anticancer therapy (radiation therapy, chemotherapy, or surgery) that have not resolved to ≤ grade 2 (as defined by CTCAE version 4.03).
  5. Inadequate bone marrow function at screening as evidenced by any of the following:

    • Absolute Neutrophil Count (ANC) < 1.5 x 109/L.
    • Platelet count < 100 x 109/L.
    • Haemoglobin < 6.0 mmol/L (< 9.6 g/dL). The patient should not have received a transfusion or growth factors for these abnormalities in the 7 days prior to Cycle 1 Day 1.
  6. Serum (total) bilirubin > 1.5 x the Upper Limit of Normal (ULN) for the institution if no liver metastases (> 2 x ULN in patients with liver metastases).
  7. AST or ALT > 2.5 x ULN if no liver metastases (> 5x ULN in patients with liver metastases).
  8. Alkaline phosphatase levels > 2.5 x ULN if no liver metastases (> 5 x ULN in patients with liver metastases, or > 10 x ULN in patients with bone metastases).
  9. Increased plasma prothrombin time or International Normalized Ratio (INR), consequence of reduced hepatic production of Vitamin K.
  10. Hepatitis B surface antigen or hepatitis C positivity with abnormal liver function tests.
  11. Medical history of:

    • Nonalcoholic steatohepatitis (NASH).
    • History of human immunodeficiency virus (HIV) antibody positive or use of antiretroviral therapy.
    • Alcoholic and autoimmune hepatitis.
    • Ischemic hepatitis, Cardiovascular dysfunction or impaired liver oxygenation, including hypotension or right heart failure.
  12. Serum creatinine > 1.5 x ULN.
  13. Estimated Glomerular Filtration Rate of < 50 mL/min/1.73m2 calculated by Modification of Diet in Renal Disease (MDRD) formula or creatinine clearance of < 50 mL/min calculated by Cockcroft-Gault.
  14. Stroke within 6 months prior to Cycle 1 Day 1.
  15. Transient Ischemic Attack (TIA) within 6 months prior to Cycle 1 Day 1.
  16. Myocardial infarction within 6 months prior to Cycle 1 Day 1.
  17. Unstable angina.
  18. New York Heart Association (NYHA) Grade II or greater Congestive Heart Failure at screening.
  19. Serious cardiac arrhythmia requiring medication.
  20. Patients who are pregnant or breastfeeding.
  21. Absence of effective means of contraception in female patients of childbearing potential (defined as <2 years after last menstruation and not surgically sterile) or in male patients who are not surgically sterile and who have female partners of childbearing potential.
  22. Major surgical procedure (including open biopsy and excluding central line intravenous catheter) within 28 days prior to the first study treatment, or anticipation of the need for major surgery during the course of the study treatment.
  23. Grade ≥2 motor or sensory neuropathy symptoms (as defined by CTCAE version 4.03).
  24. Known hypersensitivity to any of the Investigational Product's excipients or taxanes.
  25. History of drug or alcohol abuse in the opinion of the investigator within 3 years before screening.
  26. Evidence of any other medical conditions (such as psychiatric illness, infectious diseases, physical examination or laboratory findings) that may interfere with the planned treatment, affect patient compliance or place the patient at high risk for treatment-related complications.

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: CriPec® docetaxel
Docetaxel containing nanoparticle
-3 weekly IV dose. Dose escalation; start dose 15 mg/m2. Number of cycles: 6 or until progression or unacceptable toxicity develops
Altri nomi:
  • Docetaxel containing nanoparticles

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Part 1: Incidence of grade 3 or 4 adverse events (AEs) as a measure of safety and tolerability.
Lasso di tempo: 9 months
Part 1: Incidence of grade 3 or 4 adverse events (AEs) will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 1: Incidence of clinical laboratory abnormalities as a measure of safety and tolerability.
Lasso di tempo: 9 months
Part 1: Incidence of laboratory abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 1: Incidence of electrocardiogram (ECG) abnormalities as a measure of safety and tolerability.
Lasso di tempo: 9 months
Part 1: Incidence of electrocardiogram (ECG) abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1.
Lasso di tempo: 9 months
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
Lasso di tempo: 9 months
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
Lasso di tempo: 9 months
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 1 and 2: Pharmacokinetic profile of CriPec® docetaxel following IV infusion
Lasso di tempo: First two cycles of CriPec® docetaxel (each cycle is 3 weeks)
Pharmacokinetic parameters such as time to peak concentration (Tmax), peak concentration (Cmax), volume of distribution (Vd), half life (t1/2), total body clearance (CL) and area under the concentration-time curve (AUC) will be determined using plasma concentration data.
First two cycles of CriPec® docetaxel (each cycle is 3 weeks)

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Early signs of anti-tumor efficacy (overall response rate [ORR]) of CriPec® docetaxel
Lasso di tempo: 18 months in total for part 1 and 2
18 months in total for part 1 and 2
Early signs of anti-tumor efficacy (duration of response) of CriPec® docetaxel
Lasso di tempo: 18 months in total for part 1 and 2
18 months in total for part 1 and 2

Collaboratori e investigatori

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

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 (Effettivo)

1 agosto 2015

Completamento primario (Effettivo)

1 luglio 2018

Completamento dello studio (Effettivo)

1 luglio 2018

Date di iscrizione allo studio

Primo inviato

1 maggio 2015

Primo inviato che soddisfa i criteri di controllo qualità

8 maggio 2015

Primo Inserito (Stima)

13 maggio 2015

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

24 settembre 2018

Ultimo aggiornamento inviato che soddisfa i criteri QC

21 settembre 2018

Ultimo verificato

1 luglio 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 .

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