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Nivolumab and Bevacizumab in Patients With Advanced and or Metastatic Hepatocellular Carcinoma (NUANCE)

9. Dezember 2019 aktualisiert von: University of Utah

A Phase I Open Label Trial of a Combination of Nivolumab and Bevacizumab in Patients With Advanced and or Metastatic Hepatocellular Carcinoma

This is an open label, phase I study to test for maximum tolerated dose (MTD) or recommended phase II dose (RP2D) of the combination of nivolumab and bevacizumab. The study will use a 3+3 phase I study design using a fixed dose of nivolumab (240mg) and escalating doses of bevacizumab (1-10mg).

Studienübersicht

Status

Beendet

Studientyp

Interventionell

Einschreibung (Tatsächlich)

1

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Utah
      • Salt Lake City, Utah, Vereinigte Staaten, 84112
        • Huntsman Cancer Institute

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Confirmed unresectable or metastatic hepatocellular carcinoma. Confirmation either by histologic confirmation or accepted radiographic criteria.
  • Received at least one line of therapy with a TKI (including, but not limited to sorafenib, lenvatinib, and/or regorafenib) with evidence of disease progression clinically or radiographically as deemed by investigator, or refused therapy with a TKI. No more than two lines of prior therapy are allowed.
  • Measurable disease per RECIST1.1.
  • Age ≥18 years.
  • ECOG performance status of 0 to 1.
  • Life expectancy ≥ 12 weeks.
  • Childs Pugh A (5-6 points). Demonstrate adequate organ function as defined in the table below

Hematologic:

Absolute neutrophil count (ANC) ≥ 1.5 k/µL. Platelets ≥ 100 k/µL Hemoglobin ≥ 9 g/dL

Renal:

Creatinine < 2 × ULN OR

- Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.

Exclusion Criteria:

  • Prior treatment with anti-PD1 or anti-PD-L1 antibody therapy.
  • Subjects with a prior history of DVT/PE, who have not been on stable doses of anticoagulation with low molecular weight heparin or oral anticoagulant for at least two weeks.
  • History of arterial thromboembolic event in past 6 months (including CVA, MI).
  • Systemic anti-cancer treatment within 2 weeks, all ongoing adverse events related to previous systemic anti-cancer therapy resolved to grade ≤1.
  • Radiotherapy within 2 weeks of first dose of study medications.
  • Major surgery within 6 weeks of first dose of study medications. Minor procedures (e.g. port placement, endoscopy with intervention) within 4 weeks of first dose of study medications.
  • Presence of ≥ CTCAE grade 2 toxicity due to prior cancer therapy (except alopecia, peripheral neuropathy which are excluded if ≥ CTCAE grade 3).
  • Medical condition that requires chronic systemic steroid therapy, or any other form of immunosuppressive medication.
  • Active ongoing infection requiring therapy.
  • Active HIV infection.
  • History of severe hypersensitivity reaction to another monoclonal antibody.
  • Active central nervous system metastases and/or carcinomatous meningitis (stable treated brain metastases not requiring steroids >4 weeks allowed).
  • Cardiac conditions: class 3-4 New York Heart Association congestive heart failure, known baseline LVEF < 50%, transmural myocardial infarction, uncontrolled hypertension, angina pectoris requiring medication, clinically significant valvular disease, high-risk arrhythmia in the past 12 months.
  • Any history of autoimmune disease requiring treatment in the past 5 years or felt to be at risk to reactivate autoimmune disease. Patients who are felt to no longer be at risk of activating a known autoimmune disease (e.g. type 1 diabetes, ulcerative colitis s/p complete colectomy, autoimmune thyroiditis s/p thyroidectomy or medical ablation, etc.) may be allowed to participate after discussion with the PI
  • Pregnant, breast feeding, or planning to become pregnant.
  • Women of childbearing potential (WOCBP) must agree to follow instructions for method(s) of contraception for the duration of study treatment with nivolumab and 5 months after the last dose of study treatment i.e., 30 days (duration of ovulatory cycle) plus the time required for the investigational drug to undergo approximately five half-lives. Contraception as described in section 7.3
  • Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of study treatment with nivolumab and 7 months after the last dose of study treatment i.e., 90 days (duration of sperm turnover) plus the time required for the investigational drug to undergo approximately five half-lives. Contraception as described in section 7.3
  • Received any live vaccine within the last 30 days.
  • Other malignancy requiring treatment in the prior 2 years with the exception of locally treated squamous or basal cell carcinoma.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Nivolumab and bevacizumab, all patients

Nivolumab will be administered as a 240mg IV infusion given once every two weeks (+/- 3 days).

Subjects will remain on study treatment for up to two years or until progression or excessive toxicity

Andere Namen:
  • OPDIVO

Bevacizumab will be administered as an IV infusion from 1-10mg/kg in accordance with the appropriate subject cohort being examined as described below:

Dose level 1: 5 mg/kg intravenously once every two weeks Dose level 2: 10 mg/kg intravenously once every two weeks Dose level -1: 1 mg/kg intravenously once every two weeks

Dosing is based on actual body weight. There is no dose adjustment for obese or frail individuals. Dosing is recalculated if patient weight changes by more than 10% as reviewed by the principal investigator.

Subjects will remain on study treatment for up to two years or until progression or excessive toxicity

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Adverse Events that occur
Zeitfenster: Every 14 day cycle for up to 2 years - Patients are expected to be on treatment for an average of 6 months

Investigate the safety and tolerability of 14-day cycles of nivolumab plus bevacizumab.

Adverse events will be collected for each subject that received the study treatment combination.

Every 14 day cycle for up to 2 years - Patients are expected to be on treatment for an average of 6 months
Determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D)
Zeitfenster: The DLT period will begin at Cycle 1 Day 1 and continue through Cycle 1 Day 28 for each patient

Determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D).

Dose Limiting Toxicities (DLT) will define subsequent subject accrual and dose escalation

The DLT period will begin at Cycle 1 Day 1 and continue through Cycle 1 Day 28 for each patient

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Progression Free Survival (PFS)
Zeitfenster: 3 years after treatment stops

To examine the effect of the study treatment combination on the rate of progression-free survival (PFS).

Subjects will have regular imaging scans to measure disease status and response will be defined by RECIST1.1.

3 years after treatment stops
Overall Survival
Zeitfenster: 3 years after treatment stops
To examine the effect of the study treatment combination on the rate of overall survival.
3 years after treatment stops

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Mitarbeiter

Ermittler

  • Hauptermittler: Glynn W Gilcrease, MD, University of Utah

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

11. April 2018

Primärer Abschluss (Tatsächlich)

26. Juli 2018

Studienabschluss (Tatsächlich)

2. Juli 2019

Studienanmeldedaten

Zuerst eingereicht

19. Dezember 2017

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

19. Dezember 2017

Zuerst gepostet (Tatsächlich)

26. Dezember 2017

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

12. Dezember 2019

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

9. Dezember 2019

Zuletzt verifiziert

1. Dezember 2019

Mehr Informationen

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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