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Dose Escalation, Safety and Pharmacokinetic Study of SAR103168 in Patients Refractory/ Relapsed Acute Leukemias or High-risk Myelodysplastic Syndromes

26. marts 2012 opdateret af: Sanofi

A Dose Escalation Safety and Pharmacokinetic Study of SAR103168 Administered as a Single Agent by Intravenous Infusion, Once Daily for 5 Consecutive Days to Patients With Refractory/ Relapsed Acute Leukemias or High-risk Myelodysplastic Syndromes.

Primary objectives:

  • To determine the maximum tolerated dose (MTD) of SAR103168 and to characterize the dose limiting toxicities (DLTs) in the proposed dose regimen
  • To evaluate the pharmacokinetic (PK) profile of SAR103168

Secondary objectives:

  • To characterize the global safety profile of SAR103168
  • To evaluate preliminary anti-leukemia activity
  • To investigate the potential induction effect on CYP3A4 and persistence of this effect by using oral midazolam as a probe substrate in patients enrolled into the expanded cohort at the MTD
  • To determine the metabolic pathways of SAR103168 and identify the chemical structures of metabolites
  • To determine the potential impact of SAR103168 on the QTc interval in patients enrolled at the MTD

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret beskrivelse

Patients will receive the study drug until unacceptable toxicity, clinically significant disease progression, withdrawal of consent or investigator's decision, and for a maximum of 1 year.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

30

Fase

  • Fase 1

Kontakter og lokationer

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

Studiesteder

    • Georgia
      • Atlanta, Georgia, Forenede Stater, 30322
        • Sanofi-Aventis Investigational Site Number 840003
    • New York
      • New York, New York, Forenede Stater, 10021
        • Sanofi-Aventis Investigational Site Number 840002
    • Texas
      • Houston, Texas, Forenede Stater, 77030
        • Sanofi-Aventis Investigational Site Number 840001

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:

  • Patients with refractory/relapsed acute leukemias or high-risk myelodysplastic syndromes with no curative option available including any of the following:

    • Patients with de novo or secondary acute myelogenous leukemia (AML) (except acute promyelocytic leukemia), meeting one of the following conditions:
    • Refractory or relapsed AML; In case of first relapse the CR duration should be less than 12 months. If the relapse failed at least one prior salvage attempt, the CR duration may be more than 12 months.
    • Into the expanded cohort at the MTD, previously untreated AML patients over age 60 with poor- risk cytogenetics who are not eligible for or do not accept induction chemotherapy may also be included.
  • Patients with refractory/relapsed acute lymphoblastic leukemia (ALL)
  • Patients with high-risk myelodysplastic syndrome (MDS) as defined by the International Prognostic Scoring System
  • Patients with chronic myeloid leukemia in blast phase (CML-BP)

Exclusion Criteria:

  • performance status > 2
  • Active uncontrolled central nervous system leukemia
  • Cytotoxic therapy within 2 weeks prior to the first dose of SAR103168. For the non cytotoxic agents/investigational drugs this washout period should be at least 2 weeks or at least 5 half-lives whichever is longer. Hydroxyurea must be stopped at least 24 hours prior to the first dose of SAR103168
  • Lack of recovery from toxicities from prior therapies to grade < 1
  • White blood cells > 30 x 10^9/L prior to the first dose of SAR103168
  • Prior allogeneic stem cell transplantation or donor lymphocytes infusion within 3 months preceding the first dose of SAR103168
  • Any of the following within 6 months prior to the first dose of SAR103168:

    • Myocardial infarction, congestive heart failure, documented angina pectoris, arrhythmia requiring medication (in particular atrial fibrillation or flutter), severe conduction disorder (second or third atrio-ventricular block, pacemaker), coronary/peripheral artery bypass graft surgery
    • Arterial or venous thromboembolism, deep venous thrombosis
  • Left ventricular ejection fraction < 50% by echocardiography or multiple gated acquisition scan
  • Cardiac ischemia on 12-lead ECG
  • Baseline QTc-interval > 500 msec
  • Hypertension uncontrolled with appropriate therapy
  • Active infection (viral, bacterial or fungal) uncontrolled with appropriate therapy
  • Major surgery within 6 weeks prior to the first dose of SAR103168
  • Poor organ function defined by one of the following:

    • Total bilirubin > 1.5 x upper limit of normal (ULN) unless related to leukemia (i.e. hemolysis) or Gilbert's syndrome
    • Aspartate aminotransferase (AST), alanine aminotransferase (ALT) > 2.5 x ULN
    • Serum creatinine > 1.5 x ULN or calculated creatinine clearance < 50 mL/min
  • Patients under treatment with potent inhibitors of CYP3A4 unless these treatments may be stopped at least 3 days prior to the first dose of SAR103168
  • Patients under treatment with CYP3A4 or CYP2C9 inducers, unless these treatments may be stopped at least 3 days prior to the first dose of SAR103168
  • Pregnant or breast-feeding women or refusal to use adequate contraceptive method, when applicable.

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: Ikke-randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Dose escalation
Cohorts of 3 to 6 patients will be included at each dose level. The starting dose is 1.2mg/m2/day. The dose will be increased in new cohorts of patients according to toxicities observed during the first 4-week treatment period. The escalation process will continue until the MTD is determined. Additional 15 patients will be included at the MTD.

Pharmaceutical form: Concentrate for solution for infusion

Route of administration: Intravenous infusion

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Incidence of DLTs during the initial 4-week period of treatment
Tidsramme: 4 weeks
4 weeks
Pharmacokinetic parameters of SAR103168
Tidsramme: First course: Days 1, 2, 5, 6, and 8; Second and subsequent courses: Day 5 only
First course: Days 1, 2, 5, 6, and 8; Second and subsequent courses: Day 5 only

Sekundære resultatmål

Resultatmål
Tidsramme
Global safety profile of SAR103168 based on treatment emergent adverse events (TEAEs), serious adverse events (SAEs), deaths, laboratory abnormalities
Tidsramme: Treatment period up to 1 year
Treatment period up to 1 year
Preliminary evidence of anti-leukemia activity
Tidsramme: Treatment period up to 1 year
Treatment period up to 1 year
Pharmacokinetic parameters of midazolam in the absence and the presence of SAR103168.
Tidsramme: During second (Day-1 and Day 5) and forth course (Day 5)
During second (Day-1 and Day 5) and forth course (Day 5)

Samarbejdspartnere og efterforskere

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

Sponsor

Efterforskere

  • Ledende efterforsker: Farhad Ravandi-Kashani, MD, M.D. Anderson Cancer Center, Houston, Texas

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. september 2009

Primær færdiggørelse (Faktiske)

1. januar 2012

Studieafslutning (Faktiske)

1. februar 2012

Datoer for studieregistrering

Først indsendt

21. september 2009

Først indsendt, der opfyldte QC-kriterier

21. september 2009

Først opslået (Skøn)

22. september 2009

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

27. marts 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

26. marts 2012

Sidst verificeret

1. marts 2012

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 .

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