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

A Study of PLX51107 in Advanced Malignancies

20. december 2018 opdateret af: Plexxikon

A Phase 1b/2a, Two-Part, Dose Escalation and Expansion Study to Assess the Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of PLX51107 in Subjects With Advanced Hematological Malignancies and Solid Tumors

The purpose of this research study is to evaluate safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of the investigational drug PLX51107 in subjects with advanced solid tumors (including lymphoma), and advanced hematological malignancies

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

50

Fase

  • Fase 1

Kontakter og lokationer

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

Studiesteder

    • New York
      • New York, New York, Forenede Stater, 10032
        • Columbia University Medical Center
    • Ohio
      • Columbus, Ohio, Forenede Stater, 43212
        • The Ohio State University Stephanie Spielman Comprehensive Breast Center
    • Pennsylvania
      • Philadelphia, Pennsylvania, Forenede Stater, 19107
        • Thomas Jefferson University
    • South Carolina
      • Charleston, South Carolina, Forenede Stater, 29425
        • MUSC/ Hollings Cancer Center
    • Texas
      • San Antonio, Texas, Forenede Stater, 78229
        • South Texas Accelerated Research Therapeutics

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. Confirmed diagnosis of a relapsed or refractory malignancy in 1 of 2 treatment groups:

    1. Group A: Subjects with any solid tumor (including lymphomas).
    2. Group B: Subjects with relapsed or refractory AML, Subjects with relapsed or refractory high-risk MDS, defined as revised International Prognostic Scoring System (IPSS-R) intermediate or greater disease.
  2. Age ≥18 years.
  3. Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2.
  4. Life expectancy ≥3 months in the judgment of the investigator.
  5. Adequate organ function.
  6. Group A subjects must have measurable or evaluable disease per the appropriate disease criteria.
  7. Women of child-bearing potential must have a negative serum pregnancy test at Screening and must agree to use an effective form of contraception from the time of the negative pregnancy test up to 6 months after the last dose of study drug. Effective forms of contraception include abstinence, hormonal contraceptive in conjunction with a barrier method, or a double barrier method. Women of non-child-bearing potential may be included if they are either surgically sterile or have been postmenopausal for ≥1 year.
  8. Fertile men must agree to use an effective method of birth control during the study and for up to 6 months after the last dose of study drug.
  9. All associated clinically significant toxicity from previous cancer therapy must be resolved (to ≤Grade 1 or baseline) prior to study treatment administration (Grade 2 alopecia is allowed).
  10. Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.

Exclusion Criteria:

  1. Prior exposure to a bromodomain inhibitor, such as OTX-015 or CPI-0610.
  2. Allogenic or autologous transplant for hematological malignancy with infusion of stem cells within 90 days before Cycle 1 Day 1, or on active immunosuppressive therapy for graft-versus-host disease (GVHD) or GVHD prophylaxis within 2 weeks of Cycle 1 Day 1.
  3. Known uncontrolled fungal, bacterial, and/or viral infection ≥Grade 2.
  4. Uncontrolled autoimmune hemolytic anemia or thrombocytopenia.
  5. For Group A: Subjects with a history of brain metastases are ineligible. This includes previously treated brain metastases. For Group B (subjects with AML): Active symptomatic CNS involvement of AML. Subjects with previously treated leptomeningeal disease that has been effectively treated are eligible.
  6. A diagnosis of acute promyelocytic leukemia (APL) or chronic myeloid leukemia (CML) in blast crisis.
  7. Known or suspected allergy to the investigational agent or any agent given in association with this trial.
  8. Women who are pregnant or are breast feeding.
  9. Clinically significant cardiac disease
  10. Inability to take oral medication or significant nausea and vomiting, malabsorption, or significant small bowel resection that, in the opinion of the Investigator, would preclude adequate absorption.
  11. Subject with known human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) infection or is known to be a carrier of hepatitis B or C.
  12. Strong CYP3A4 and CYP2C8 inhibitors or inducers or CYP3A4 substrate drugs with a narrow therapeutic range taken within 14 days or 5 drug half-lives before start of study drug.
  13. Active secondary malignancy
  14. Major surgery or significant traumatic injury within 14 days prior to therapy
  15. Receipt of anti-cancer therapy 14 days prior to Cycle 1 Day 1
  16. Presence of any other medical, psychological, familial, sociological, or geographic condition potentially hampering compliance with the study protocol Subjects who are participating in any other therapeutic clinical study (observational or registry trials are allowed).
  17. Subjects who have Burkitt's lymphoma or Burkitt-like lymphoma.
  18. Subjects on active anticoagulation therapy including warfarin, factor Xa inhibitors, thrombin inhibitors, or heparin.
  19. Subjects with documented hepatic metastases involving >50% of the hepatic parenchyma.

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: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Treatment Group A
Open label, sequential PLX51107 dose escalation in approximately 30 solid tumor subjects.
Eksperimentel: Treatment Group B
Open label, sequential PLX51107 dose escalation in approximately 30 subjects with acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS).

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Safety of PLX51107 as measured by adverse events and serious adverse events.
Tidsramme: 1 year
1 year
Area under the concentration-time curve (AUC) of PLX51107.
Tidsramme: 1 year
1 year
Maximum observed concentration (Cmax) of PLX51107.
Tidsramme: 1 year
1 year
Time to peak concentration (Tmax) of PLX51107.
Tidsramme: 1 year
1 year
Half life (t1/2) of PLX51107.
Tidsramme: 1 year
1 year

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Overall Response Rate (ORR)
Tidsramme: 1 year
ORR is defined as the total number of patients with the best overall response according to standard criteria for the relevant malignancy divided by the total number of treated patients and expressed as a percentage.
1 year
Duration Of Response (DOR).
Tidsramme: 1 year
DOR is defined as the time from the initial objective response to disease progression or death, whichever occurs first.
1 year
Progression-Free Survival (PFS).
Tidsramme: 1 year
PFS time is defined as the time from the first dose of PLX51107 to disease progression or death, whichever occurs first.
1 year
Overall Survival (OS).
Tidsramme: 1 year
OS is defined as the first dose of study drug until the date of death from any cause.
1 year

Samarbejdspartnere og efterforskere

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

Sponsor

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. marts 2016

Primær færdiggørelse (Faktiske)

1. september 2018

Studieafslutning (Faktiske)

1. september 2018

Datoer for studieregistrering

Først indsendt

12. februar 2016

Først indsendt, der opfyldte QC-kriterier

12. februar 2016

Først opslået (Skøn)

17. februar 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

24. december 2018

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

20. december 2018

Sidst verificeret

1. december 2018

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

UBESLUTET

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 .

Abonner