Onvansertib in Combination With Nanoliposomal Irinotecan, Leucovorin, and Fluorouracil for Second-Line Treatment of Participants With Metastatic Pancreatic Ductal Adenocarcinoma

NCT ID: NCT04752696

Last Updated: 2025-12-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

41 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-25

Study Completion Date

2024-12-24

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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 pancreatic ductal adenocarcinoma (PDAC).

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pancreatic Ductal Adenocarcinoma

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Pancreatic Ductal Adenocarcinoma Onvansertib Nanoliposomal irinotecan Leucovorin Fluorouracil PLK1 PLK Inhibitor

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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).

Group Type EXPERIMENTAL

Onvansertib

Intervention Type DRUG

Oral capsule

Nanoliposomal irinotecan

Intervention Type DRUG

Intravenous infusion

Leucovorin

Intervention Type DRUG

Intravenous infusion

Fluorouracil

Intervention Type DRUG

Intravenous infusion

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).

Group Type EXPERIMENTAL

Onvansertib

Intervention Type DRUG

Oral capsule

Nanoliposomal irinotecan

Intervention Type DRUG

Intravenous infusion

Leucovorin

Intervention Type DRUG

Intravenous infusion

Fluorouracil

Intervention Type DRUG

Intravenous infusion

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Onvansertib

Oral capsule

Intervention Type DRUG

Nanoliposomal irinotecan

Intravenous infusion

Intervention Type DRUG

Leucovorin

Intravenous infusion

Intervention Type DRUG

Fluorouracil

Intravenous infusion

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

PCM-075 Onivyde Nal-IRI 5-FU

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cardiff Oncology

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Mayo Clinic Phoenix

Phoenix, Arizona, United States

Site Status

Mayo Clinic Jacksonville

Jacksonville, Florida, United States

Site Status

University of Kansas Medical Center

Westwood, Kansas, United States

Site Status

Mayo Clinic Rochester

Rochester, Minnesota, United States

Site Status

University of Nebraska Medical Center

Omaha, Nebraska, United States

Site Status

Inova Schar Cancer Institute

Fairfax, Virginia, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CRDF-001

Identifier Type: -

Identifier Source: org_study_id