転移性膵管腺癌の参加者の二次治療のためのナノリポソームイリノテカン、ロイコボリン、およびフルオロウラシルと組み合わせたオンバンセルチブ
転移性膵管腺癌患者の二次治療のためのナノリポソームイリノテカン、ロイコボリン、およびフルオロウラシルと組み合わせたオンバンセルチブの第2相試験
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.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- フェーズ2
連絡先と場所
研究場所
-
-
Arizona
-
Phoenix、Arizona、アメリカ、85054
- Mayo Clinic Phoenix
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-
Florida
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Jacksonville、Florida、アメリカ、32224
- Mayo Clinic Jacksonville
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Kansas
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Westwood、Kansas、アメリカ、66205
- University of Kansas Medical Center
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Minnesota
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Rochester、Minnesota、アメリカ、55905
- Mayo Clinic Rochester
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Nebraska
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Omaha、Nebraska、アメリカ、68198
- University of Nebraska Medical Center
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-
Virginia
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Fairfax、Virginia、アメリカ、22031
- Inova Schar Cancer Institute
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-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的: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
他の名前:
Intravenous infusion
他の名前:
Intravenous infusion
他の名前:
|
|
実験的: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
他の名前:
Intravenous infusion
他の名前:
Intravenous infusion
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Response Rate (ORR) Per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
時間枠: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
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Survival (OS)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- CRDF-001
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。