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Onvansertib i kombination med nanoliposomal irinotecan, leucovorin og fluorouracil til andenlinjebehandling af deltagere med metastatisk pancreas ductal adenocarcinom

3. november 2026 opdateret af: Cardiff Oncology

Et fase 2-studie af Onvansertib i kombination med nanoliposomal irinotecan, leucovorin og fluorouracil til andenlinjebehandling af patienter med metastatisk pancreas ductal adenocarcinom

The main objective of this trial is to assess the efficacy of onvansertib in combination with nanoliposomal irinotecan (nal-IRI), leucovorin, and fluorouracil (5-FU) for treatment of participants with histologically confirmed metastatic PDAC.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

41

Fase

  • Fase 2

Kontakter og lokationer

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

Studiesteder

    • Arizona
      • Phoenix, Arizona, Forenede Stater, 85054
        • Mayo Clinic Phoenix
    • Florida
      • Jacksonville, Florida, Forenede Stater, 32224
        • Mayo Clinic Jacksonville
    • Kansas
      • Westwood, Kansas, Forenede Stater, 66205
        • University of Kansas Medical Center
    • Minnesota
      • Rochester, Minnesota, Forenede Stater, 55905
        • Mayo Clinic Rochester
    • Nebraska
      • Omaha, Nebraska, Forenede Stater, 68198
        • University of Nebraska Medical Center
    • Virginia
      • Fairfax, Virginia, Forenede Stater, 22031
        • Inova Schar Cancer Institute

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:

  • Histologically or cytologically confirmed metastatic PDAC
  • Has received 1 prior gemcitabine-based chemotherapy as first line therapy for metastatic disease. Progression after completion of neoadjuvant or adjuvant therapy of < 6 months in duration is considered 1 line of therapy for metastatic disease
  • Has measurable disease according to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1), defined as at least 1 lesion that can be accurately measured in at least 1 dimension (longest diameter to be recorded) as > 20 mm with conventional techniques or as > 10 mm with spiral computed tomography (CT) scan
  • Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
  • Must be willing and able to undergo a tissue biopsy at screening; participants who, in the opinion of the investigator, do not have tissue that is accessible for biopsy are excepted from this criterion
  • Women of childbearing potential: (defined as not post-menopausal for 12 months or no previous surgical sterilization) and fertile men must agree to use adequate contraception for the duration of study participation and for 4 months after the last dose of nal-IRI. Male subjects must agree to refrain from sperm donation during the study and for 4 months after the last dose of nal-IRI
  • Ability to understand and the willingness to sign a written informed consent document. Signed informed consent form must be obtained prior to initiation of study evaluations and/or activities
  • International Normalized Ratio (INR) < 1.5 unless on warfarin
  • Participants with prior malignancy and who were treated with no evidence of active disease more than 2 years from initial diagnosis are eligible
  • Age ≥ 18 years
  • Participants must have adequate organ and bone marrow function

Exclusion Criteria:

  • Prior treatment with irinotecan, nal-IRI, or investigational PLK1 inhibitor
  • Uncontrolled intercurrent illness including symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, and myocardial infarction within 3 months of initiation of therapy
  • History of interstitial pneumonitis or interstitial lung disease
  • Participants with microsatellite instability-high (MSI-H) tumors with no prior immune checkpoint inhibitor exposure
  • Pregnancy or lactation
  • Participant has active and uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy
  • QT interval with Fridericia's correction (QTcF) > 470 milliseconds. The QTcF should be calculated as the arithmetic mean of the QTcF on triplicate electrocardiograms (ECGs). In the case of potentially correctible causes of QT prolongation, (eg, medications, hypokalemia), the triplicate ECG may be repeated once during Screening and that result may be used to determine eligibility
  • Planned concomitant use of medications known to prolong the QT/QTc interval
  • Participant has undergone major surgical resection within 4 weeks prior to enrollment
  • Participant received radiotherapy, surgery, chemotherapy, or an investigational therapy within 2 weeks prior to study entry
  • Participant has serious medical risk factors involving any of the major organ systems such that the investigator considers it unsafe for the participant to receive an experimental research drugs
  • Serious psychiatric or medical conditions that could interfere with treatment
  • Major bleeding in the last 4 weeks
  • More than 1 prior chemotherapy regimen administered in the metastatic setting
  • Unable or unwilling to swallow oral medication
  • Use of strong CYP3A4 or UGT1A1 inhibitors or strong CYP3A4 inducers. Participants currently receiving these agents who are able to switch to alternate therapy are not excluded. Inhibitors should be stopped at least one week prior to the first dose of protocol therapy and inducers should be stopped at least two weeks prior to initiation of protocol therapy.

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: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Safety Lead-in: Onvansertib + nal-IRI + leucovorin + 5-FU

The first 3 participants will be administered onvansertib orally once a day at a dosing schedule of 12 mg/m^2 on Day 1 to Day 10 for two cycles, where each cycle is 2 weeks. Depending on the number of dose limiting toxicities (DLTs) experienced in the first 3 participants, additional participants may receive different dosing schedules, determining the dosing schedule to be used in the treatment period. Onvansertib will be administered in combination with 70 mg/m^2 nanoliposomal irinotecan (nal-IRI), 400 mg/m^2 leucovorin and 2400 mg/m^2 fluorouracil (5-FU).

Intravenous infusion

Oral capsule

Andre navne:
  • PCM-075

Intravenous infusion

Andre navne:
  • Onivyde
  • Nal-IRI

Intravenous infusion

Andre navne:
  • 5-FU
Eksperimentel: Treatment Period: Onvansertib + nal-IRI + leucovorin + 5-FU

Participants will be administered onvansertib at the dosing schedule selected based on the results of the safety lead-in, in cycles of 2 weeks. Onvansertib will be administered in combination with 70 mg/m^2 nanoliposomal irinotecan (nal-IRI), 400 mg/m^2 leucovorin and 2400 mg/m^2 fluorouracil (5-FU).

Intravenous infusion

Oral capsule

Andre navne:
  • PCM-075

Intravenous infusion

Andre navne:
  • Onivyde
  • Nal-IRI

Intravenous infusion

Andre navne:
  • 5-FU

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Overall Response Rate (ORR) Per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
Tidsramme: Up to approximately 91 weeks

ORR was defined as the percentage of participants who achieved a best overall response of confirmed complete reponse (CR) or partial response (PR) determined by the Investigator per RECIST v1.1.

According to RECIST 1.1, a CR is the disappearance of all target lesions, with non-target lesions non-existent and no new lesions and a PR is a decrease of at least 30% in the sum of the diameters of target lesions, as long as there are no new lesions and non-target lesions have not worsened.

Two-sided 95% confidence interval (CI) was calculated using the exact binomial Clopper-Pearson method.

Up to approximately 91 weeks

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Overall Survival (OS)
Tidsramme: Up to approximately 21 months

OS was calculated as: OS = (date of death - date of first dose of study treatments + 1)/ 30.4375.

95% CI was estimated using the Kaplan-Meier method.

Up to approximately 21 months
Duration of Response (DOR)
Tidsramme: Up to approximately 91 weeks

DOR was calculated as: DOR = (date of recurrence or progression of disease or all-cause death - date of first confirmed CR or PR + 1)/30.4375. Only participants who had a confirmed CR or PR were included in the analysis, and the percentage was based on the number of participants who had such a response.

95% CI was estimated using the Kaplan-Meier method.

Up to approximately 91 weeks
Number of Participants Who Experienced Treatment-emergent Adverse Events (TEAEs)
Tidsramme: Up to approximately 91 weeks

TEAEs were defined as AEs that first occurred or worsened in severity on or after the first administration of trial treatments and up to 30 days after the last administration of trial treatments.

Up to approximately 91 weeks
Disease Control Rate (DCR)
Tidsramme: Up to approximately 91 weeks

DCR was defined as the percentage of participants who achieved a best overall response of confirmed CR or PR, or stable disease (SD) determined by the Investigator per RECIST v1.1.

Two-sided 95% CI was calculated using the exact binomial Clopper-Pearson method.

Up to approximately 91 weeks

Samarbejdspartnere og efterforskere

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

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 (Faktiske)

25. maj 2021

Primær færdiggørelse (Faktiske)

24. december 2024

Studieafslutning (Faktiske)

24. december 2024

Datoer for studieregistrering

Først indsendt

9. februar 2021

Først indsendt, der opfyldte QC-kriterier

9. februar 2021

Først opslået (Faktiske)

12. februar 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

4. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. november 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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