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Obinutuzumab With High-dose Ibrutinib for the Treatment of Patients With Chronic Lymphocytic Leukemia With Progressive Disease on Single Agent Ibrutinib.

23. januar 2019 oppdatert av: Michael Choi

A Phase 1 Clinical Trial to Evaluate Obinutuzumab With High-dose Ibrutinib for the Treatment of Patients With Chronic Lymphocytic Leukemia With Progressive Disease on Single Agent Ibrutinib.

The purpose of the study is to investigate whether the combination of obinutuzumab and ibrutinib (administered up to 840 mg per day) might be useful for the treatment of CLL or SLL that is not responding or no longer responding to treatment with ibrutinib alone. The study will evaluate whether this regimen can reduce the amount of cancerous cells in the body. Subjects will be treated with ibrutinib at a dose of up to 840 mg a day by mouth, as well as obinutuzumab infusions. Although both of these agents are approved by the FDA for the treatment of CLL or SLL, the combination and the dosing schedule of ibrutinib are considered experimental.

Studieoversikt

Status

Tilbaketrukket

Detaljert beskrivelse

This is phase 1 study for patients with CLL or small lymphocytic lymphoma (SLL) experiencing disease progression on single ibrutinib. This study will evaluate the optimal ibrutinib dose (including doses higher than 420 mg) when combined with obinutuzumab.

During the screening period, patients will continue on ibrutinib at their previous tolerated dose, unless required to stop (e.g.: by a preceding clinical trial).

On cycle 1, day 1, the dose of ibrutinib will be assigned based on the dose cohort. Patients in cohort 1 will receive ibrutinib 420 mg PO daily. Patients in cohort 2 will receive ibrutinib 560 mg PO daily. Cohort 3 will be 700 mg PO daily. Cohort 4 will be 840 mg PO daily.

On cycle 1, day 1, patients will also initiate treatment with obinutuzumab (100 mg on day 1, 900mg on day 2, 1000mg day 8, 15, 28 then q 28 days for a total of 8 doses).

The primary safety endpoint is determination of DLTs during the first 28 days. The primary efficacy endpoint of overall response rate will be assessed 2 months after the final dose of obinutuzumab.

Studietype

Intervensjonell

Fase

  • Fase 1

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:

  • Clinical and phenotypic verification of B cell CLL or SLL and measurable disease.
  • Prior therapy: Patients must have been receiving single agent ibrutinib therapy at the time of disease progression. Patient may have received other therapy in combination with ibrutinib earlier in the their treatment course. Prior obinutuzumab therapy is also permitted.
  • Progressive disease on current single agent ibrutinib therapy (but not within the first 2 months of initiating ibrutinib therapy). Progression is based on 2008 iwCLL definition.
  • ECOG performance status of 0-2.
  • Adequate hematologic function.
  • Adequate renal function.
  • Adequate hepatic function.

Exclusion Criteria:

  • Known CNS lymphoma or leukemia
  • History of Richter's or prolymphocytic transformation.
  • Primary ibrutinib resistance, defined by progressive disease within the first 2 months of first initiating ibrutinib therapy.
  • Uncontrolled autoimmune hemolytic anemia (AIHA) or idiopathic thrombocytopenia purpura (ITP)
  • CLL therapy, with the exception of ibrutinib within the following timeframes:

    1. Chemotherapy, external beam radiation therapy, anticancer antibodies within 30 days prior to the first dose of drug on this study.
    2. Corticosteroid use 20mg prednisone within 1 week prior to first dose on this study.
    3. Radio- or toxin-conjugated antibody therapy within 10 weeks prior to first dose on this study.
    4. Allogeneic stem cell transplant within 6 months prior to first dose on this study
  • History of major surgery within 4 weeks prior to first dose on this study.
  • History of prior malignancy, with the exception of adequately treated non-melanoma skin cancer, malignancies treated with curative intent and with no evidence of active disease for more than 3 years, or adequately treated cervical carcinoma in situ without current evidence of disease.
  • Currently active clinically significant cardiovascular disease or history of myocardial infarction within 6 months of first dose.
  • Serologic status and/or PCR testing reflecting active hepatitis B or C infection.
  • Known history of infection with human immunodeficiency virus (HIV).
  • Unable to swallow capsules or disease significantly affecting gastrointestinal function.
  • History of stroke or intracranial hemorrhage within 6 months of first dose.
  • Requires anticoagulation with warfarin or other Vitamin K antagonists.
  • Requires treatment with a strong CYP 3A inhibitor.
  • Pregnant or breast-feeding women
  • Women of child-bearing age must obtain a pregnancy test and pregnant or breast feeding females
  • Patients who are currently receiving another investigational therapy
  • Current infection requiring parenteral antibiotics.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: ibrutinib +obinutuzumab
Cohort 1 420 mg PO daily Cohort 2 560 mg PO daily Cohort 3 700 mg PO daily Cohort 4 840 mg PO daily
Andre navn:
  • Imbruvica
obinutuzumab 100 mg IV on day 1, 900mg IV on day 2, 1000mg IV day 8, 15, 28 then q 28 days for a total of 8 doses.
Andre navn:
  • Gazyva

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Maksimal tolerert dose
Tidsramme: 2 måneder
2 måneder

Sekundære resultatmål

Resultatmål
Tidsramme
Treatment-emergent adverse events
Tidsramme: 2 years
2 years
samlet svarprosent
Tidsramme: 2 måneder
2 måneder
progresjonsfri overlevelse
Tidsramme: 2 måneder
2 måneder
stable disease rate
Tidsramme: 2 months
2 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

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. juni 2016

Primær fullføring (Forventet)

1. november 2019

Studiet fullført (Forventet)

1. november 2020

Datoer for studieregistrering

Først innsendt

19. november 2015

Først innsendt som oppfylte QC-kriteriene

19. november 2015

Først lagt ut (Anslag)

23. november 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

25. januar 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

23. januar 2019

Sist bekreftet

1. januar 2019

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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. .

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