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A Study of the Histone-deacetylase Inhibitor JNJ-26481585 in Patients With Advanced or Refractory Leukemia or Myelodysplastic Syndrome

A Phase 1 Study of the Histone-deacetylase Inhibitor JNJ-26481585 in Subjects With Advanced or Refractory Leukemia or Myelodysplastic Syndrome

The purpose of this study is to explore the safety, pharmacokinetic (what the body does to the medication), pharmacodynamic (what the medication does to the body), and activity of JNJ-26481585 in patients with advanced or refractory leukemia and myelodysplastic syndrome (MDS).

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret beskrivelse

This is an open-label (all people know the identity of the intervention), Phase 1 dose escalation, 2-part study (Part I and Part II). In Part I of the study, the Maximum Tolerated Dose (MTD) defined as the highest dose with an observed incidence of dose limiting toxicity (DLT) in no more than 1 in 6 patients, will be determined using rapid escalation (Stage 1) followed by conventional escalation (Stage 2). In Stage 1, at least 2 patients will be enrolled at each dose level; dose increments of 100% will be applied. In Stage 2, at least 3 patients will be enrolled at each dose level and dose increments of 20-50% will be implemented. Decisions on dose escalation or de-escalation, changes in the timing of pharmacokinetic/pharmacodynamic sampling, and the exploration of an alternative schedule were to be made by the Study Evaluation Team (SET), which consisted of all principal investigators, the medical monitor, and 1 of the sponsor's clinical pharmacologists. Part II of the study will be the expansion phase, which will begin after the MTD had been determined in Part I and an additional cohort of patients with MDS will be enrolled to further explore the safety and activity of JNJ 26481585 in patients with MDS. The starting dose for patients enrolled in Part II of the study was to be the MTD established in Part I. Depending on the outcome, the SET may decide to continue at the MTD dose, or dose-de-escalate to the next lower level (25 50% decrement from MTD). The cohort for MDS will be expanded to consist of 16 evaluable patients. Safety will be evaluated throughout the study and will include evaluations of adverse events clinical laboratory tests, electrocardiogram (ECG), vital signs, 24 hours Holter ECG, physical examination, Eastern Cooperative Oncology Group performance status and Multiple Gated Acquisition scan or echocardiography.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

10

Fase

  • Fase 1

Kontakter og lokationer

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

Studiesteder

    • Maryland
      • Baltimore, Maryland, Forenede Stater
    • Texas
      • Houston, Texas, Forenede Stater

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:

  • Histologically or cytologically confirmed advanced or refractory acute myeloid leukemia, acute lymphocytic leukemia, chronic myeloid leukemia in blast phase, refractory chronic lymphocytic leukemia, myelodysplastic syndrome, or chronic myelomonocytic leukemia
  • For Part II, patients with myelodysplastic syndrome
  • Eastern Cooperative Oncology Group Performance Status Score 0, 1 or 2
  • Left Ventricular Ejection Fraction greater than or equal to 50%
  • Negative hepatitis B, C and human immunodeficiency virus (HIV) test within last 3 months
  • Adequate liver and kidney function

Exclusion Criteria:

  • Known or suspected involvement of the central nervous system
  • Chemotherapy (nitrosoureas and mitomycin C within 6 weeks), radiotherapy, immunotherapy or treatment with investigative agent within 3 weeks before study drug administration (except hydroxyurea which should be stopped at least 24 hours prior to first dose)
  • Unstable angina or myocardial infarction within the preceding 12 months; congestive heart failure
  • Poorly controlled hypertension or diabetes, ongoing active infection and psychiatric illness
  • Receiving medications known to have a risk of causing QTc prolongation

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: JNJ-26481585
In Part 1, Initial dose of JNJ-26481585 4 mg oral capsule is administered once daily on each day of a 21-day cycle. Dose will be escalated or de-escalated until Maximum tolerated dose (MTD) of JNJ-26481585 is determined in Part 1. MTD of JNJ-26481585 will be the initial dose in Part 2.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number of patients with adverse events
Tidsramme: Upto 14 days after last dose administration of study medication
Upto 14 days after last dose administration of study medication
Number of patients with dose limiting toxicity [DLT]
Tidsramme: From the date of dosing upto 3 months after the date the last patient enrolled in Part I of the study, received the first dose of study medication
Only toxicities that occur during Treatment Cycle 1 will be used for the purposes of defining DLT.
From the date of dosing upto 3 months after the date the last patient enrolled in Part I of the study, received the first dose of study medication
Maximum tolerated dose (MTD) of JNJ 26481585
Tidsramme: From the date of dosing upto 3 months after the date the last patient enrolled in Part I of the study, received the first dose of study medication
The MTD is defined as the highest dose with an observed incidence of DLT in no more than 1 in 6 patients.
From the date of dosing upto 3 months after the date the last patient enrolled in Part I of the study, received the first dose of study medication

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Maximum plasma concentration (Cmax) of JNJ 26481585
Tidsramme: Days 1, 2, 8, 15 and 21 of Cycle 1
Days 1, 2, 8, 15 and 21 of Cycle 1
Time to reach maximum plasma concentration (tmax) of JNJ-26481585
Tidsramme: Days 1, 2, 8, 15 and 21 of Cycle 1
Days 1, 2, 8, 15 and 21 of Cycle 1
Area under the plasma concentration-time curve from time 0 to 24 hours (AUC0-24)
Tidsramme: Days 1, 2, 8, 15 and 21 of Cycle 1
Days 1, 2, 8, 15 and 21 of Cycle 1
Elimination half-life (t1/2) of JNJ-26481585
Tidsramme: Days 1, 2, 8, 15 and 21 of Cycle 1
Days 1, 2, 8, 15 and 21 of Cycle 1
Cumulative amount of drug excreted in urine over 24 hours (Ae24)
Tidsramme: Days 1 and 21 of Cycle 1
Days 1 and 21 of Cycle 1
Renal clearance (CLR) of JNJ 26395018
Tidsramme: Days 1 and 21 of Cycle 1
Days 1 and 21 of Cycle 1
Concentration of biomarker histone acetylation
Tidsramme: Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Concentration of biomarker interleukin-6 (IL-6)
Tidsramme: Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Concentration of biomarker heat shock protein 90 (Hsp90)
Tidsramme: Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Days 1 and 21 of Cycle 1; Day 21 of Cycles 2 to 20
Complete Blood Count (CBC)
Tidsramme: Pre-treatment (within 4 weeks prior to first dose of JNJ-26481585); Days 1, 3, 8, 15 and 21 of Cycle 1; Days 8, 15 and 21 of Cycle 2; Day 21 of Cycle 3 to 20; follow up (within 14 days after last dose of JNJ-26481585)
Anticancer activity of JNJ-26481585 explored by assessment of response parameters such as CBC.
Pre-treatment (within 4 weeks prior to first dose of JNJ-26481585); Days 1, 3, 8, 15 and 21 of Cycle 1; Days 8, 15 and 21 of Cycle 2; Day 21 of Cycle 3 to 20; follow up (within 14 days after last dose of JNJ-26481585)
Assessment of Transfusion Record
Tidsramme: From Day 1 of Cycle 1 upto 14 days after last dose
Assessment of Transfusion Record is the parameter for assessment of response.
From Day 1 of Cycle 1 upto 14 days after last dose
Radiological Tumor Mass assessment
Tidsramme: Pre-treatment, Day 21 of Cycle 2 to 20 and follow up
Radiological Tumor Mass assessment is the parameter for assessment of response.
Pre-treatment, Day 21 of Cycle 2 to 20 and follow up
Bone marrow aspirate/biopsy assessment
Tidsramme: Pre-treatment, Day 21 of Cycles 1 to 20
Bone marrow aspirate/biopsy assessment is the parameter for assessment of response.
Pre-treatment, Day 21 of Cycles 1 to 20

Samarbejdspartnere og efterforskere

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

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

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

1. december 2008

Primær færdiggørelse (Faktiske)

1. september 2011

Studieafslutning (Faktiske)

1. september 2011

Datoer for studieregistrering

Først indsendt

8. maj 2008

Først indsendt, der opfyldte QC-kriterier

12. maj 2008

Først opslået (Skøn)

13. maj 2008

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

14. september 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

13. september 2012

Sidst verificeret

1. september 2012

Mere information

Begreber relateret til denne undersøgelse

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 .

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