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Study Evaluating Safety And Tolerability, Solid Tumor

2018年4月24日 更新者:Puma Biotechnology, Inc.

A Phase 1 Study Of Neratinib (HKI-272) In Combination With Paclitaxel In Subjects With Solid Tumors

This is an open-label, phase 1 study of ascending multiple oral doses of HKI-272 in combination with paclitaxel.

調査の概要

研究の種類

介入

入学 (実際)

10

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Shizuoka、日本
        • Investigational Site
      • Tokyo、日本
        • Investigational Site

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

20年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Subjects must have confirmed pathologic diagnosis of a solid tumor that is not curable with available therapy for which HKI-272 plus paclitaxel is a reasonable treatment option.
  • At least 1 measurable lesion as defined by RECIST criteria.
  • Eastern Cooperative Oncology Group (ECOG) 0 to 1
  • LVEF within institutional limits of normal (by MUGA or ECHO).
  • Screening laboratory values within the following parameters:

    • ANC: greater than or equal to 1.5 x 10E9 /L (1,500 /mm3)
    • Platelet count: 10 x 10E10 /L (100,000 /mm3)
    • Hemoglobin: greater than or equal to 9.0 g/dL
    • Serum creatinine: less than or equal to 1.5 x upper limit of normal (ULN)
    • Total bilirubin: less than or equal to 1.5 xULN · AST and ALT: less than or equal to 2.5 xULN (less than or equal to 5 x ULN if liver metastases are present)
  • For women of child bearing potential, a negative urine or serum pregnancy test result before study entry. A woman of childbearing potential is one who is biologically capable of becoming pregnant. This includes women who are using contraceptives or other means of birth control or whose sexual partners are either sterile or using contraceptives.
  • All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 28 days after the last dose of test article.

Exclusion Criteria:

  • Prior treatment with anthracyclines with a cumulative dose of doxorubicin of greater than 400 mg/m^2, epirubicin dose of greater than 800 mg/m^2, or the equivalent dose for other anthracyclines or derivatives.
  • Major surgery, chemotherapy, radical (curative intent) radiotherapy, investigational agents, or other cancer therapy within 2 weeks of treatment day 1 or non-recovery from all clinically significant acute adverse effects of prior therapies (excluding alopecia).
  • Subjects with bone or skin as the only site of disease.
  • Active central nervous system (CNS) metastases, as indicated by clinical symptoms, cerebral edema, and/or progressive growth (subjects with a history of CNS metastases or cord compression are allowable if they have been definitively treated and have been clinically stable for at least three months, and off steroids or anticonvulsants, before first dose of test article).
  • QTc interval greater than 0.47 second or known history of QTc prolongation or Torsade de Pointes (TdP).
  • Known hypersensitivity to paclitaxel or Cremophor EL (polyoxyethylated castor oil).
  • Pregnant or breast feeding women.
  • Significant chronic or recent acute gastrointestinal disorder with diarrhea as a major symptom (e.g., Crohn's disease, malabsorption, or Grade greater than or equal to 2 diarrhea of any etiology at baseline).
  • Inability or unwillingness to swallow the HKI-272.
  • Treatment with a taxane within 3 months of treatment day 1.
  • Pre-existing grade 2 or greater motor or sensory neuropathy.
  • Any other cancer within 5 years prior to screening with the exception of contralateral breast carcinoma, adequately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin.
  • Presence of clinically significant or uncontrolled cardiac disease, including congestive heart failure (New York Heart Association [NYHA] functional classification of greater than or equal to 2), angina requiring treatment, myocardial infarction within the past 12 months, or any clinically significant supraventricular arrhythmia or ventricular arrhythmia requiring treatment or intervention.
  • Evidence of significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, make the subject inappropriate for this study. Examples include, but are not limited to, serious active infection (ie, requiring intravenous antibiotic or antiviral agent), uncontrolled major seizure disorder, or significant pulmonary disorder (e.g. interstitial pneumonitis, pulmonary hypertension).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Nera 160 + Pac
Neratinib 160 mg + Paclitaxel 80 mg/m^2
Administered orally, continuous, once daily.
他の名前:
  • HKI-272
Administered IV, on days 1, 8, 15 of 28 day cycle.
実験的:Nera 240 + Pac
Neratinib 240 mg + Paclitaxel 80 mg/m^2
Administered orally, continuous, once daily.
他の名前:
  • HKI-272
Administered IV, on days 1, 8, 15 of 28 day cycle.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Dose Limiting Toxicity (DLT) - Percentage of Participants With DLT Events
時間枠:From first dose day through day 28.
The incidence of DLTs in subjects with advanced solid tumors, treated with neratinib in combination with paclitaxel 80 mg/m^2. DLT was defined as any neratinib plus paclitaxel related Grade 3 or 4 nonhematologic toxicity or Grade 4 hematologic toxicity with few exceptions.
From first dose day through day 28.
Maximum Tolerated Dose
時間枠:From first dose day through day 28.
The maximum tolerated dose of neratinib, as determined by the incidence of DLTs, in combination with paclitaxel 80 mg/m^2, in subjects with advanced solid tumors.
From first dose day through day 28.

二次結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate
時間枠:From first dose date to progression/death or last tumor assessment, up to 78 weeks.
Percentage of participants with partial response (PR) or complete response (CR) per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0: Complete Response (CR), disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
From first dose date to progression/death or last tumor assessment, up to 78 weeks.
Progression Free Survival
時間枠:From first dose date to progression/death, up to 78 weeks.
Number of weeks between the date of the first dose of test article and the first date of disease recurrence or progression, or death due to any cause, was documented, censored at the last evaluation, investigator assessment. Progression is defined using Response Evaluation Criteria in Solid Tumors Criteria (v1.0), as at least a 20% increase in the sum of the longest diameters (LD) of target lesions, taking as reference the nadir LD, meaning the smallest sum of the LDs recorded since the treatment started; or unequivocal progression of existing nontarget lesions; or the appearance of any new lesions.
From first dose date to progression/death, up to 78 weeks.
Duration of Response
時間枠:From start date of response to first disease progression, up to 71 weeks.
Number of weeks from the time at which measurement criteria are met for Complete Response (CR) or Partial Response (PR) (whichever status is recorded first) until the first date on which recurrence or progressive disease (PD) is objectively documented, taking as reference for PD the smallest measurements recorded since the treatment started, for responders only, per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0: CR, disappearance of all target lesions; PR, >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
From start date of response to first disease progression, up to 71 weeks.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2008年10月1日

一次修了 (実際)

2011年1月1日

研究の完了 (実際)

2011年1月1日

試験登録日

最初に提出

2008年10月7日

QC基準を満たした最初の提出物

2008年10月7日

最初の投稿 (見積もり)

2008年10月8日

学習記録の更新

投稿された最後の更新 (実際)

2018年11月19日

QC基準を満たした最後の更新が送信されました

2018年4月24日

最終確認日

2018年4月1日

詳しくは

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。

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