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Mitoxantrone Hydrochloride Liposome Injection, Bortezomib and Dexamethasone in the Treatment of R/R MM

A Phase Ⅰ Clinical Study of Mitoxantrone Hydrochloride Liposome Injection in Combination With Bortezomib and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

The purpose of this study is to evaluate the safety and efficacy of mitoxantrone hydrochloride liposome injection in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma.

調査の概要

詳細な説明

This is a multicenter, open-label, phase I study aimed to evaluate the safety and efficacy of mitoxantrone hydrochloride liposome injection in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma. In the study, 60 patients will be recruited into three dose groups. All patients will receive the treatment for the planned 8 cycles(28 days per cycle)until disease progression or unacceptable drug-related adverse events

研究の種類

介入

入学 (予想される)

60

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。

研究連絡先

研究場所

    • Beijing
      • Beijing、Beijing、中国
        • 募集
        • Beijing Chaoyang Hospital, Capital Medical University
        • コンタクト:

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

18年~75年 (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:

  1. Patients fully understand and voluntarily participate in this study and sign informed consent;
  2. Aged 18-75 years, without gender limitation;
  3. Patients with relapsed or refractory multiple myeloma(confirmed by histologically or cytologically) who had received at least one prior line regular treatment;
  4. Patients have at least one of the following conditions:(1)Serum M protein≥10g/L;(2)Urine M protein≥200 mg/24h; (3)Serum free light chain(sFLC): κ/λ FLC ratio is abnormal and affected FLC ≥100mg /L
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2;
  6. Laboratory tests meet the following conditions:

    • Absolute neutrophil count (ANC) ≥1.5x10^9/L (No G-CSF treatment within 1 week prior to the laboratory test);
    • Platelet count ≥ 75x10^9/L (No platelet transfusion within 1 week prior to the laboratory test);
    • Total bilirubin ≤1.5upper limit of normal (ULN);
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 ULN;
    • Creatinine clearance(Ccr) ≥30mL/min.
  7. Females of childbearing potential must have a negative serum beta human chorionic gonadotrophin (β-hCG) pregnancy test result prior to enrollment and must agree to use an effective contraception method for the duration of the study treatment and 7 months after the last dose of study therapy.
  8. Males patients and their partners must agree to use an effective contraceptive method for the duration of the study treatment and 4 months after the last dose of study therapy.

    -

Exclusion Criteria:

  1. Patients with amyloidosis or central nervous system invasion or on dialysis treatment.
  2. Life expectancy < 3 months.
  3. History of allergy to mitoxantrone hydrochloride or liposomes;or previous treatment with adriamycin or other anthracyclines, with the total cumulative dose (doxorubicin equivalent) ≥350 mg/m^2.
  4. History of allergy (except local injection reaction) or intolerance to bortezomib;or one of the following conditions occurred with prior bortezomib regimens: no treatment response (not reach MR),disease progression within 6 months after the end of last dose.
  5. History of contraindications or intolerance to dexamethasone.
  6. Any anti-myeloma drug treatment or radiotherapy within 4 weeks prior to the first dose; or enrolled in any other clinical trials of anti-myeloma drug within 3 months prior to the first dose.
  7. History of autologous hematopoietic stem cell transplantation within 6 months prior to screening.
  8. History of allogeneic hematopoietic stem cell transplantation or solid organ transplantation.
  9. Adverse events from the previous treatment have not resolved to ≤ Grade 1 (except for alopecia, hyperpigmentation).
  10. Patients with persistent Grade≥2 peripheral neuropathy or Grade 1 peripheral neuropathy with pain.
  11. Patients with impaired cardiac function or significant cardiac disease.
  12. HBsAg/HBcAb positive with HBV-DNA titer higher than the lower limit of the test value of the research center, or HCV antibody positive with HCV-RNA titer higher than the lower limit of the test value of the research center,or human immunodeficiency virus (HIV) antibody positive.
  13. Patients with obvious digestive system dysfunction, which may affect intake, transport and absorption of the study drug.
  14. Active bacterial, fungal or viral infections that require systemic treatment within 1 week prior to the first dose
  15. Patients underwent major surgery within 6 weeks prior to the first dose, or had a surgical schedule during the study period;
  16. History of additional malignant tumor within 5 years, except for locally curable cancer that has been cured.
  17. Other medical conditions that, in the judgment of the investigator, may affect the patient's participation in this study.
  18. Pregnant or breastfeeding women;
  19. Not suitable for this study as decided by the investigator due to other reasons.

    -

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: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:12 mg/m ^ 2 dose group (ArmA)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 12 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
他の名前:
  • ミトキサントロン塩酸塩リポソーム
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
他の名前:
  • ボルテゾミブ
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
他の名前:
  • デキサメタゾン
実験的:16 mg/m ^ 2 dose group (ArmB)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 16 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
他の名前:
  • ミトキサントロン塩酸塩リポソーム
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
他の名前:
  • ボルテゾミブ
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
他の名前:
  • デキサメタゾン
実験的:20 mg/m ^ 2 dose group (ArmC)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 20 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
他の名前:
  • ミトキサントロン塩酸塩リポソーム
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
他の名前:
  • ボルテゾミブ
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
他の名前:
  • デキサメタゾン

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
Treatment-emergent adverse events (TEAEs)
時間枠:From the initiation of the first dose to 28 days after the last dose
To indentify the incidence of TEAEs
From the initiation of the first dose to 28 days after the last dose

二次結果の測定

結果測定
メジャーの説明
時間枠
Objective response rate (ORR)
時間枠:Throughout the study treatment(Up to 32 weeks)
ORR is defined as the proportion of patients who have a best overall response of partial response (PR),very good partial response(VGPR), complete response (CR) or stringent complete response (sCR) as per International Myeloma Working Group (IMWG)
Throughout the study treatment(Up to 32 weeks)
Clinical Benefit Rate(CBR)
時間枠:Throughout the study treatment(Up to 32 weeks)
CBR is defined as the proportion of patients who have a best overall response of minimal response(MR),PR,VGPR,CR or sCR as per IMWG
Throughout the study treatment(Up to 32 weeks)
Disease control rate(DCR)
時間枠:Throughout the study treatment(Up to 32 weeks)
DCR is defined as the proportion of patients who have a best overall response of stable disease (SD),MR,PR,VGPR,CR or sCR as per IMWG
Throughout the study treatment(Up to 32 weeks)
Duration of response (DoR)
時間枠:Throughout the study completion.(An average of 12 months)
DoR is defined as the time from the first assessment of PR,VGPR,CR orsCR until the date of first occurrence of progressive disease (PD) as per IMWG
Throughout the study completion.(An average of 12 months)
Progression-free survival (PFS)
時間枠:Throughout the study completion.(An average of 12 months)
PFS is defined as the time from the date of first dose until the date of first documented PD as per IMWG or death from any cause, whichever occurs first
Throughout the study completion.(An average of 12 months)
Overall survival (OS)
時間枠:Throughout the study completion.(An average of 36 months)
OS is defined as the time from the date of first dose until the date of death from any cause
Throughout the study completion.(An average of 36 months)

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。

捜査官

  • 主任研究者:Wenming Chen、Beijing Chaoyang Hospital Affiliated to Capital Medical University

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)

2021年10月20日

一次修了 (予想される)

2023年4月20日

研究の完了 (予想される)

2024年6月20日

試験登録日

最初に提出

2021年9月13日

QC基準を満たした最初の提出物

2021年9月13日

最初の投稿 (実際)

2021年9月22日

学習記録の更新

投稿された最後の更新 (実際)

2022年2月1日

QC基準を満たした最後の更新が送信されました

2022年1月16日

最終確認日

2022年1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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