- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02683395
A Study of PLX51107 in Advanced Malignancies
20. desember 2018 oppdatert av: 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
Studieoversikt
Status
Avsluttet
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
50
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
New York
-
New York, New York, Forente stater, 10032
- Columbia University Medical Center
-
-
Ohio
-
Columbus, Ohio, Forente stater, 43212
- The Ohio State University Stephanie Spielman Comprehensive Breast Center
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Forente stater, 19107
- Thomas Jefferson University
-
-
South Carolina
-
Charleston, South Carolina, Forente stater, 29425
- MUSC/ Hollings Cancer Center
-
-
Texas
-
San Antonio, Texas, Forente stater, 78229
- South Texas Accelerated Research Therapeutics
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
Confirmed diagnosis of a relapsed or refractory malignancy in 1 of 2 treatment groups:
- Group A: Subjects with any solid tumor (including lymphomas).
- 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.
- Age ≥18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2.
- Life expectancy ≥3 months in the judgment of the investigator.
- Adequate organ function.
- Group A subjects must have measurable or evaluable disease per the appropriate disease criteria.
- 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.
- 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.
- 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).
- Willingness and ability to provide written informed consent prior to any study-related procedures and to comply with all study requirements.
Exclusion Criteria:
- Prior exposure to a bromodomain inhibitor, such as OTX-015 or CPI-0610.
- 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.
- Known uncontrolled fungal, bacterial, and/or viral infection ≥Grade 2.
- Uncontrolled autoimmune hemolytic anemia or thrombocytopenia.
- 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.
- A diagnosis of acute promyelocytic leukemia (APL) or chronic myeloid leukemia (CML) in blast crisis.
- Known or suspected allergy to the investigational agent or any agent given in association with this trial.
- Women who are pregnant or are breast feeding.
- Clinically significant cardiac disease
- 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.
- 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.
- 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.
- Active secondary malignancy
- Major surgery or significant traumatic injury within 14 days prior to therapy
- Receipt of anti-cancer therapy 14 days prior to Cycle 1 Day 1
- 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).
- Subjects who have Burkitt's lymphoma or Burkitt-like lymphoma.
- Subjects on active anticoagulation therapy including warfarin, factor Xa inhibitors, thrombin inhibitors, or heparin.
- Subjects with documented hepatic metastases involving >50% of the hepatic parenchyma.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Treatment Group A
Open label, sequential PLX51107 dose escalation in approximately 30 solid tumor subjects.
|
|
|
Eksperimentell: Treatment Group B
Open label, sequential PLX51107 dose escalation in approximately 30 subjects with acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS).
|
Hva måler studien?
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 |
Tiltaksbeskrivelse |
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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2016
Primær fullføring (Faktiske)
1. september 2018
Studiet fullført (Faktiske)
1. september 2018
Datoer for studieregistrering
Først innsendt
12. februar 2016
Først innsendt som oppfylte QC-kriteriene
12. februar 2016
Først lagt ut (Anslag)
17. februar 2016
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
24. desember 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. desember 2018
Sist bekreftet
1. desember 2018
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i immunsystemet
- Neoplasmer etter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Lymfesykdommer
- Immunproliferative lidelser
- Benmargssykdommer
- Hematologiske sykdommer
- Forstadier til kreft
- Leukemi
- Lymfom
- Myelodysplastiske syndromer
- Leukemi, myeloid
- Leukemi, Myeloid, Akutt
- Lymfom, Non-Hodgkin
- Preleukemi
Andre studie-ID-numre
- PLX122-01
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
UBESLUTTE
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .