A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493 in Patients With Advanced or Refractory Solid Tumors or Lymphoma
2019年5月13日 更新者:Janssen Research & Development, LLC
A Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493, a Pan-Fibroblast Growth Factor Receptor (FGFR) Tyrosine Kinase Inhibitor, in Subjects With Advanced or Refractory Solid Tumors or Lymphoma
The purpose of this study is to determine a dose for future development and to evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy profiles of JNJ-42756493 in Japanese and other Asian patients with advanced or refractory solid tumors or lymphoma.
調査の概要
詳細な説明
This is an open-label (identity of assigned study drug will be known), multicenter, 2-part, Phase 1 dose escalation/expansion to evaluate the safety, pharmacokinetics (study of what the body does to a drug), pharmacodynamics (study of what a drug does to the body) and clinical activity of JNJ-42756493 administered orally once daily in 21-day cycles or 28 days cycles of intermittent dosing regimen (7 days on/7 days off) to Japanese and Asian participants >=20 years of age with advanced or refractory solid tumors or lymphoma who are not candidates for approved or available therapies.
Approximately 40 participants will be enrolled.
In Part 1 Participants will be required to be hospitalized after the first dose on Day 1 of Cycle 1 until Day 2 of Cycle 2 (for daily continuous dosing) or until Day 14 of Cycle 1 (for intermittent dosing), however extension of hospitalization will be allowed until Day 2 of Cycle 2 according to investigators clinical judgment.
The Part 1 dose-escalation phase is designed to determine the recommended Phase 2 dose (RP2D) based on safety, pharmacokinetic, and pharmacodynamic data of JNJ-42756493.
Participants will be enrolled in sequential cohorts based on the 3+3 dose-escalation scheme; the first cohort will receive the starting dose and subsequent cohorts will receive increased doses of JNJ-42756493.
After the last participants in each cohort completes Cycle 1, the Safety Evaluation Team (SET) will evaluate the safety and pharmacokinetic data according to protocol-defined criteria and make the decision whether to escalate the dose in a new cohort.
To determine the recommended Phase 2 dose, the SET will review all safety, pharmacokinetic, and pharmacodynamic data from Part 1 before initiation of Part 2. The total number of participants enrolled in Part 1 will depend on the dose level at which the recommended Phase 2 dose is established.
After the recommended Phase 2 dose is established, the Part 2 dose-expansion phase will be opened.
Part 2 study will be done in a molecularly-defined subset of Participants with gastric adenocarcinoma including gastroesophageal junctions at the RP2D.
In Part2, Participants can be hospitalized until Day 8 of Cycle 1 as needed.
In addition, extension of hospitalization will be allowed until Day 15 of Cycle 1 according to investigator's clinical judgment.
In Part 2, approximately 25 participants will be treated at the recommended Phase 2 dose as 28 days cycles of intermittent dosing regimen in order to evaluate fibroblast growth factor receptor target modulation in tumor, to further elaborate safety, pharmacokinetics, and pharmacodynamics of JNJ-42756493, as well as to evaluate preliminary clinical responses.
Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
Serial pharmacokinetic and pharmacodynamic samples will be collected, and safety and efficacy will be monitored throughout the study.
研究の種類
介入
入学 (実際)
19
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
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Kashiwa、日本
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Matsuyama、日本
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Tokyo、日本
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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:
- Part 1: Histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative treatment is no longer effective
- Part 2: Histologically or cytologically confirmed gastric adenocarcinoma including gastroesophageal junctions that is metastatic, locally advanced or unresectable, and for which standard treatment is no longer effective or tolerable
- Eastern Cooperative Oncology Group performance status score 0 or 1
- Adequate bone marrow, liver, and renal function according to protocol-defined criteria within the 7 days prior to Day 1 of Cycle 1
- Laboratory values within protocol -defined parameters
- Agrees to protocol-defined use of effective contraception
- Negative urine pregnancy test (urine or serum beta human chorionic gonadotropin [beta-HCG]) at screening for women of child bearing potential
Exclusion Criteria:
- Has had chemotherapy, radiotherapy, immunotherapy, or treatment with an investigational anticancer agent within 3 weeks (nitrosoureas and mitomycin C within 6 weeks) before the first administration of study drug (localized radiation therapy for palliative purposes and ongoing luteinizing hormone-releasing hormone agonists and antagonists for patients with prostate cancer, bisphosphonates and denosumab are permitted
- History or current condition of uncontrolled cardiovascular disease as defined in the protocol
- Taking medications known to have a risk of causing QTc prolongation and Torsades de Pointes or known as strong CYP3A inhibitors or inducers
- Left ventricular ejection fraction less than (<) 50 percent (%) as assessed by echocardiography (or multi-gated acquisition [MUGA]) performed at screening
- Uncontrolled intercurrent illness including, but not limited to, poorly controlled hypertension or diabetes, ongoing active infection, psychiatric illness, or a risk of gastrointestinal perforation
Woman who is pregnant, breast-feeding, or planning to become pregnant or is a man who plans to father a child, while the participant is enrolled in this study and is within 3 or 5 months, respectively, after the last dose of the study drug
- Not recovered from reversible, clinically significant toxicity of prior anticancer therapy
- Presence of any medical condition that requires intact wound healing capacity and is expected to endanger participant safety if wound healing capacity would be severely reduced during administration of the investigational agent
- Major surgery within 4 weeks before enrollment
- Known human immunodeficiency virus infection
- Known hepatitis B or C (except hepatocellular carcinoma)
- Active, symptomatic, or untreated brain metastasis
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 |
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実験的:Part 1: Dose Escalation (Daily Dosing)
Dose escalation of JNJ-42756493 is to occur until a dose at which <33 percent of participants experience a dose-limiting toxicity, the maximum concentration of JNJ-42756493 is less than the protocol-defined cardiovascular threshold, and JNJ-42756493 is biologically active.
Participants will receive study drug once day on Day 1 of Cycle 1 followed by a 2-day drug-free period (Days 2 and 3 of Cycle 1) and continues throughout the 21 day cycle.
For all subsequent cycles once a day for 21 days.
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JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
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実験的:Part 1: Dose Escalation (Intermittent Dosing)
Intermitting dosing regimen will be 28 days (7 days on and 7 days off).
Participants will receive JNJ-42756493 on Days 1 to 7 and Days 15 to 21 of each cycle; JNJ-42756493 will not be administered on Days 8 to 14 and Days 22 to 28 of each cycle.
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JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
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実験的:Part 2: Dose Expansion
Participants will receive the recommended Phase 2 JNJ-42756493 dose determined in Part 1 as Intermitting dosing regimen (28 days, 7 days on and 7 days off).
Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
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Recommended Phase 2 JNJ-42756493 dose determined in Part 1 administered orally for 28-days cycles (Intermitting dosing regimen).
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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 |
時間枠 |
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MedDRA システム臓器クラス (SOC) および優先用語 (PT) による有害事象の影響を受けた参加者の数
時間枠:治験薬の最終投与後30日まで
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治験薬の最終投与後30日まで
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Maximum observed plasma concentration of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Minimum observed plasma concentration of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Time correspondent to the maximum observed plasma concentration of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Area under the plasma concentration-time curve from time 0 to 24 hours of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Half-life of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Apparent volume of distribution of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Total clearance of drug of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Accumulation index of JNJ-42756493
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Number of participants with complete response
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with partial response
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with stable disease
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with progressive disease
時間枠:Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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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。
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
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)
2013年8月21日
一次修了 (実際)
2016年1月28日
研究の完了 (実際)
2016年1月28日
試験登録日
最初に提出
2013年7月26日
QC基準を満たした最初の提出物
2013年10月10日
最初の投稿 (見積もり)
2013年10月14日
学習記録の更新
投稿された最後の更新 (実際)
2019年5月15日
QC基準を満たした最後の更新が送信されました
2019年5月13日
最終確認日
2019年5月1日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- CR102388
- 42756493GAC1001 (その他の識別子:Janssen Research & Development, LLC)
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。