A Study of Rocbrutinib in Combination With Lacutoclax in Patients With B-Cell Malignancies
A Phase Ib/II, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of BTK Inhibitor Rocbrutinib in Combination With BCL-2 Inhibitor Lacutoclax in Patients With B-Cell Malignancies
調査の概要
状態
条件
介入・治療
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Lugui Qiu
- 電話番号:+86-13821266636
- メール:qiulg@ihcams.ac.cn
研究場所
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-
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Tianjin、中国
- 募集
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
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コンタクト:
- Lugui Qiu
- 電話番号:+86-13821266636
- メール:qiulg@ihcams.ac.cn
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-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Age ≥18 years, regardless of sex.
Ib: Histologically confirmed diagnosis of CLL/SLL (per 2018 iwCLL criteria) or B-cell malignancies (per 2022 WHO classification), including: MCL, DLBCL, FL, and WM. Must have received at least one prior line of systemic therapy, with documented disease progression or intolerance.
II: For Treatment-naïve (TN) CLL/SLL patients: Must meet iwCLL treatment indications and no prior systemic therapy. For R/R CLL/SLL patients: at least one prior systemic therapy with documented disease progression or intolerance.
- Have at least one measurable lesion.
- Phase Ib: ECOG performance status ≤1; phase II: ECOG performance status ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of study treatment. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity or intolerance to Rocbrutinib, Lacutoclax, or any of their excipients; prior treatment with any BCL-2 inhibitor; or prior treatment with both covalent and non-covalent BTK inhibitors.
- Use of systemic corticosteroids at doses equivalent to >20 mg/day of prednisone for ≥3 days within 7 days prior to the first dose.
- History of or currently suspected Richter's syndrome.
- Known or suspected central nervous system (CNS) involvement.
- Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
- Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
- Received herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
- Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to prior to the first dose.
- History of other active malignancies within the past 3 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
- Any severe and/or uncontrolled systemic disease, or any other condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.
- Any of the following events within 6 months prior to the first dose: Symptomatic arrhythmia, myocardial infarction, intracranial hemorrhage, or Stroke.
- Impaired cardiac function.
- Any uncontrolled systemic infection.
- Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
- Unable to discontinue moderate or strong CYP3A inhibitors or inducers, P-gp (P-glycoprotein) inhibitors, sensitive substrates of OATP1B3 or CYP2C8 during the study period.
- Received vaccination with any live-attenuated vaccines within 4 weeks prior to the first dose of study treatment.
- Evidence of an active bleeding constitution or a history of significant hemorrhagic disorders.
- Requirement for ongoing therapy with warfarin or other vitamin K antagonists.
- Presence of an active, uncontrolled, or symptomatic autoimmune disease that requires systemic treatment.
- Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.
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:なし
- 介入モデル:単一グループの割り当て
- 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:Lacutoclax+Rocbrutinib
|
Phase Ib dose-escalation study of Rocbrutinib in combination with Lacutoclax. Rocbrutinib will be administered at a fixed dose of 150 mg once daily (QD), while Lacutoclax will be dose-escalated. Initial dose levels include Lacutoclax 200 mg QD and 400 mg QD in 28-day treatment cycles.Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. In phase II, participants will receive Rocbrutinib monotherapy for 8-12 weeks prior to combination treatment. Upon initiation of combination therapy, Lacutoclax will undergo dose ramp-up to the target dose and will then be administered continuously at the target dose. Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. |
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 |
|---|---|
|
Phase Ib: Dose-limiting toxicity (DLT)
時間枠:At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: Maximum Tolerated Dose (MTD)
時間枠:At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: Adverse events as assessed by CTCAE v5.0
時間枠:From the first administration to 28 days after the last administration
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From the first administration to 28 days after the last administration
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Phase Ib: Time to Maximum Plasma Concentration (Tmax)
時間枠:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Maximum Plasma Concentration (Cmax)
時間枠:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
時間枠:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Half-life (t1/2)
時間枠:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
|
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Phase II: Undetectable minimal residual disease (uMRD) rate assessed by flow cytometry
時間枠:Up to approximately three years
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Up to approximately three years
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Phase II: Maximum Plasma Concentration (Cmax)
時間枠:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
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Phase II: Time to Maximum Plasma Concentration (Tmax)
時間枠:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
Phase II: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
時間枠:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
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Phase II: Half-life (t1/2)
時間枠:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Overall Response Rate(ORR)
時間枠:Up to approximately three years
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Up to approximately three years
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Progression-free Survival(PFS)
時間枠:Up to approximately three years
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Up to approximately three years
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Overall Survival(OS)
時間枠:Up to approximately three years
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Up to approximately three years
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Phase II: Adverse events as assessed by CTCAE v5.0
時間枠:From the first administration to 28 days after the last administration
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From the first administration to 28 days after the last administration
|
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Complete Response Rate (CRR)
時間枠:Up to approximately three years
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Up to approximately three years
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Duration of Response (DOR)
時間枠:Up to approximately three years
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Up to approximately three years
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Phase Ib: Undetectable Minimal Residual Disease (uMRD) Rate assessed by flow cytometry
時間枠:Up to approximately three years
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Up to approximately three years
|
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)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
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
- LP-10822
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
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