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Ein DNAJB1-PRKACA-Fusionskinase-Peptidimpfstoff kombiniert mit dem Glutamin-Antagonisten DRP-104, Nivolumab und Ipilimumab bei Patienten mit fortgeschrittenem Fibrolamellärem Karzinom (FLC)

Eine Phase-1b-Studie eines DNAJB1-PRKACA-Fusionskinase-Peptidimpfstoffs in Kombination mit dem Glutamin-Antagonisten DRP-104, Nivolumab und Ipilimumab für Patienten mit fortgeschrittenem fibrolamellären hepatozellulären Karzinom (FLC)

The purpose of this study is to determine whether the combination of a neoantigen vaccine targeting the DNAJB1-PRKACA fusion kinase in combination with DRP-104, Nivolumab and Ipilimumab is safe and yields a clinically compelling antitumor activity measured as based on objective response rate (ORR, assessed by RECIST 1.1). Secondary objectives include progression-free survival (PFS) and overall survival (OS).

Studienübersicht

Status

Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

27

Phase

  • Phase 1

Kontakte und Standorte

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

Studienkontakt

Studienorte

    • Maryland
      • Baltimore, Maryland, Vereinigte Staaten, 21231
        • Rekrutierung
        • Johns Hopkins SKCCC
        • Kontakt:
        • Hauptermittler:
          • Marina Baretti, MD

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

12 Jahre und älter (Kind, Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Must have histologically confirmed FLC that is metastatic or unresectable.
  • Presence of DNAJB1-PRKACA fusion transcript, assessed by RNA-sequencing, DNA-sequencing, or in situ hybridization in the archival tissue.
  • Must have demonstrated radiographic progression on prior or current immunotherapy.
  • Age ≥ 12 years.
  • Patients < 18 years old must have a body weight ≥ 40 kg.
  • ECOG (Eastern Cooperative Oncology Group) performance status of ≤2
  • Patients must have adequate organ and marrow function defined by study-specified laboratory tests.
  • Patients must have adequate kidney and liver function defined by study-specified laboratory tests.
  • Must have measurable disease per RECIST 1.1
  • Willingness to provide tissue and blood samples for mandatory translational research.
  • Women of childbearing potential (WOCBP) must have a negative urine or serum pregnancy test.
  • For both Women and Men, must use acceptable form of birth control while on study.
  • Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria:

  • Patients with a history of prior treatment with checkpoint inhibitors, such as anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, anti-OX-40, anti-CD40, anti-CTLA-4, or anti-LAG-3 antibodies.

  • Must have had chemotherapy or other systemic therapy or radiotherapy, as follows:

    • Patients who have had chemotherapy, biological cancer therapy, or radiation 14 days prior to the first dose of study drug.
    • Patients who have had surgery within 28 days of dosing of investigational agent, excluding minor procedures.
    • Patients who have received other approved or investigational agents or device within 28 days of the first dose of study drug.
  • Patients who have not recovered from acute adverse events to grade ≤1 or baseline due to agents administered, with exception of grade 2 fatigue, rash, and endocrinopathy successfully managed hormone replacement therapy, or alopecia or stable neuropathy, unless approved by the IND Sponsor.

  • Patients who have received any non-oncology live vaccine therapy used for prevention of infectious diseases within 28 days of study treatment.

  • Known sensitivity to or history of allergic reactions attributed to compounds of similar chemical or biologic composition of polyinosinic-polycytidylic acid (Poly-ICLC) and/or DRP-104 and/or nivolumab and/or ipilimumab.

  • History of severe hypersensitivity reaction to any monoclonal antibody.

  • Has an active autoimmune disease.

  • Prior allogeneic stem cell transplantation or organ transplantation.

  • Has a diagnosis of immunodeficiency.

  • Systemic corticosteroids at immunosuppressive doses.

  • Subjects with interstitial lung disease that is symptomatic or may interfere with the detection or management of suspected drug-related pulmonary toxicity.

  • Has a pulse oximetry of <92% on room air or is on supplemental home oxygen.

  • Active or untreated brain metastases or leptomeningeal metastases.

  • Uncontrolled intercurrent active medical and/or psychiatric illness/social psychosocial problems that that would limit compliance with study requirements.

  • Uncontrolled intercurrent illness including, but not limited to, uncontrolled infection, symptomatic congestive heart failure, unstable angina, cardiac arrhythmia, metastatic cancer, or psychiatric illness/social situations that would limit compliance with study requirements.

  • Pregnant or breastfeeding.

  • Has a known history of Human Immunodeficiency Virus (HIV)/AIDS.

  • Has active hepatitis B. Patients with chronic or acute HBV infection.

  • Have had evidence of active or acute diverticulitis, intra-abdominal abscess, or GI obstruction which are known risk factors for bowel perforation should be evaluated for the potential need for additional treatment before coming on study.

  • Unwilling or unable to follow the study schedule for any reason.

  • Patient is at the time of signing informed consent a regular user (including "recreational use") of any illicit drugs or had a recent history (within the last year) of substance abuse (including alcohol).

  • Evidence of clinical ascites.

  • Patients with QTc prolongation > 470 ms according to Fridericia formula.

  • Patients receiving potent inducers of CYP 3A4/5 (including but not limited to apalutamide, carbamazepine, enzalutamide, mitotane, phenytoin, rifampin and St. John's Wort) who cannot safely discontinue drug at least 14 days prior to Cycle 1 Day 1.

  • Have had an allergen hyposensitization therapy within 2 weeks prior to initiation of study treatment.

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: Arm A - DNAJB1-PRKACA-Peptidimpfstoff mit poly-ICLC-Adjuvans, DRP-104, Nivolumab und Ipilimumab
  1. Patients will receive treatment on Day 1, 8 and 15 of cycle 1 and on Day 1 of cycle 2, 3, and 4 (Prime Phase). Boost vaccinations will be administered every 3 cycles beginning from C5D1.
  2. Drug: 0.3 mg DNAJB1-PRKACA peptide vaccine + 0.5 mg Poly-ICLC
Andere Namen:
  • Hiltonol® (Poly-ICLC)
  1. Patients will receive treatment on Day 1, 4, 8, 11, 15, and 18 of cycle 1-4 (Prime Phase) then on Days 1, 4, 8, 11, 15, 18, 22 and 25 of each cycle starting on Day 1 of Cycle 5 (Boost/maintenance Phase). DRP-104 will be administered as a subcutaneous injection twice a week (BIW) on a continuous schedule for up to two years.
  2. Drug: 145 mg
  1. Patients will receive treatment on Day 1 of each Cycle. Nivolumab 3mg/kg will be administered every 3 weeks as a 30 minute IV infusion (-10/+15min) on Day 1 of Cycle 1-4 (Prime Phase). Nivolumab infusions will be administered as a flat dose of 480mg every 4 weeks starting on Day 1 of Cycle 5 (Boost/maintenance).
  2. Drug: 3mg/kg and 480mg IV
Andere Namen:
  • OPDIVO
  1. Patients will receive treatment on Day 1 of Cycle 1-4 (Prime Phase). Ipilimumab (1 mg/kg) will be administered. Ipilimumab (1 mg/kg) will be administered as a 30 minute IV infusion (-10/+15min).
  2. Drug: 1mg/kg IV
Andere Namen:
  • YERVOY®

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of participants experiencing grade 3 or above drug-related toxicities
Zeitfenster: 4 years

When calculating the incidence of AEs, each AE (as defined by NCI CTCAE v6.0) will be counted only once for a given subject.

4 years
Objective response rate (ORR) using immune Response Evaluation Criteria for Solid Tumors (RECIST 1.1)
Zeitfenster: 4 years

ORR is defined as the percentage of patients achieving a complete response (CR) or partial response (PR) to DRP-104 in combination with DRP-104, Nivolumab and Ipilimumab, based on the immune Response Evaluation Criteria in Solid Tumors (RECIST 1.1) at any time during the study. CR = disappearance of all target lesions, PR is =>30percent decrease in sum of diameters of target lesions, progressive disease (PD) is >20percent increase in sum of diameters of target lesions, stable disease (SD) is <30percent decrease or <20percent increase in sum of diameters of target lesions.

4 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Progression-free Survival (PFS) number of months according to RECIST (1.1) criteria.
Zeitfenster: 4 years

PFS is defined as the number of months from the date of first treatment to disease progression (progressive disease [PD] or relapse from complete response [CR] as assessed using RECIST 1.1 criteria) or death due to any cause. Per RECIST 1.1 criteria, CR = disappearance of all target lesions, Partial Response (PR) is =>30% decrease in sum of diameters of target lesions, Progressive Disease (PD) is >20% increase in sum of diameters of target lesions, Stable Disease (SD) is <30% decrease or <20% increase in sum of diameters of target lesions.

4 years
Overall survival (OS) of patients treated with study drug combination
Zeitfenster: 4 years

OS is defined as the number of months from the first dose of study treatment to death from any cause. (OS will be censored on the date the subject was last known to be alive for subjects without documentation of death at the time of analysis). Estimation based on the Kaplan-Meier curve.

4 years

Mitarbeiter und Ermittler

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

Sponsor

Mitarbeiter

Ermittler

  • Hauptermittler: Marina Baretti, MD, SKCCC • Johns Hopkins Medical Institution

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)

28. Oktober 2026

Primärer Abschluss (Geschätzt)

1. Oktober 2030

Studienabschluss (Geschätzt)

1. Oktober 2030

Studienanmeldedaten

Zuerst eingereicht

18. Februar 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

18. Februar 2026

Zuerst gepostet (Tatsächlich)

24. Februar 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

30. Oktober 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

29. Oktober 2026

Zuletzt verifiziert

1. Oktober 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • J2622
  • IRB00541955 (Andere Kennung: Johns Hopkins Medicine Institutional Review Board)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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