Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

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

21. september 2018 opdateret af: 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.

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret beskrivelse

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

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

33

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Leuven, Belgien
        • University Hospital Leuven
      • Amsterdam, Holland
        • VUMC Amsterdam
      • Groningen, Holland
        • UMC Groningen
      • Rotterdam, Holland
        • Erasmus Medical Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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
Andre navne:
  • Docetaxel containing nanoparticles

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Part 1: Incidence of grade 3 or 4 adverse events (AEs) as a measure of safety and tolerability.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tidsramme
Early signs of anti-tumor efficacy (overall response rate [ORR]) of CriPec® docetaxel
Tidsramme: 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
Tidsramme: 18 months in total for part 1 and 2
18 months in total for part 1 and 2

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. august 2015

Primær færdiggørelse (Faktiske)

1. juli 2018

Studieafslutning (Faktiske)

1. juli 2018

Datoer for studieregistrering

Først indsendt

1. maj 2015

Først indsendt, der opfyldte QC-kriterier

8. maj 2015

Først opslået (Skøn)

13. maj 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

24. september 2018

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. september 2018

Sidst verificeret

1. juli 2018

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med CriPec® docetaxel

3
Abonner