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Addition of Hydroxyurea to Fludarabine, Cytarabine, Idarubicin and Venetoclax Salvage Therapy for Adults With Relapsed or Refractory Acute Myeloid Leukemia (FLAsH-IV-AML)

2026年8月11日 更新者:Christer C Nilsson

FLAsH-IV-AML: A Phase I/II Multi-center Study to Assess the Tolerability and Efficacy of the Addition of Hydroxyurea to Salvage Treatment With Fludarabine, Ara-C, Idarubicin and Venetoclax for Adults With Relapsed or Refractory Acute Myeloid Leukemia

This study is evaluating a new treatment approach for adults with acute myeloid leukemia (AML) that has either returned after previous treatment or has not responded to treatment. Outcomes for these patients are often poor, and there is a need for more effective therapies.

The study is investigating whether adding hydroxyurea to a combination of established AML medicines (fludarabine, cytarabine, idarubicin, and venetoclax) is safe and tolerable and can improve treatment results. Laboratory studies suggest that hydroxyurea may help leukemia cells become more sensitive to treatment and may increase the effectiveness of chemotherapy.

The study is being conducted in two parts. In the first part, researchers will determine the safest and most appropriate dose of hydroxyurea when given together with the study treatment. In the second part, researchers will evaluate whether adding hydroxyurea improves treatment outcomes, including the length of time patients remain free from disease progression, relapse, or death.

The overall goal of the study is to determine whether adding hydroxyurea to standard treatment for relapsed or refractory AML is safe and may improve patient outcomes.

調査の概要

状態

まだ募集していません

条件

介入・治療

研究の種類

介入

入学 (推定)

26

段階

  • フェーズ2
  • 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

      • Stockholm、スウェーデン
        • Medical Unit Hematology, Karolinska University Hospital
        • コンタクト:
        • 主任研究者:
          • Christer C Nilsson, MD PhD

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. A diagnosis of either:

    • Refractory AML defined as having > 10% bone marrow blasts after induction with one cycle of intensive chemotherapy or no CR after two cycles of chemotherapy.
    • Relapsed disease (including extramedullary disease) according to the 2022 ELN criteria (see appendix A).
    • MRD relapse defined as evidence of measurable (minimal) residual disease (MRD) at a level of ≥5%, as determined by either molecular assays or multiparameter flow cytometry.
  2. Age 18 years or older.
  3. ECOG Performance Status ≤ 2.
  4. Adequate renal and hepatic functions as indicated by the following laboratory values:

    • Creatinine clearance ≥ 30 mL/min calculated by the Cockcroft Gault formula.
    • Serum bilirubin ≤ 3 x upper limit of normal (ULN), unless due to Gilbert's syndrome.
    • Alanine aminotransferase (ALAT) ≤ 5 x ULN.
  5. Considered fit for intensive chemotherapy.
  6. Male patients must use a latex condom during any sexual contact with women of childbearing potential, even if they have undergone a successful vasectomy and must agree to avoid fathering a child (while on therapy and for 6 months after the final study drug administration). In addition, their female partners of childbearing potential must use a highly effective method of birth control.
  7. Male patient must not donate sperm starting at screening and throughout the study period and for 6 months after the final study drug administration.
  8. Female patients of nonchildbearing potential must be postmenopausal (defined as at least 1 year without any menses), documented surgically sterile prior to screening.
  9. Female patients of childbearing potential must agree to avoid pregnancy during the study and for 6 months after the final study drug administration and have a negative urine or serum pregnancy test at screening, and if heterosexually active, agree to consistently apply one highly effective method of birth control in combination to a barrier method for the duration of the study and for 6 months after the final study drug administration.
  10. The subject has given their written consent to participate in the trial.
  11. Patient is capable of giving informed consent.

Exclusion Criteria:

  1. Acute promyelocytic leukemia.
  2. WBC ≥30; pretreatment with HU to reduce the level of WBC <30 is allowed in part B/phase II of the trial.
  3. TP53 double hit mutation / biallelic TP53 inactivation.
  4. CNS leukemia.
  5. Relapse within 3 months from the date of allo-HCT.
  6. Uncontrolled infection.
  7. ECOG Performance Status > 2.
  8. Major organ failure precluding administration of planned chemotherapy
  9. Cardiac dysfunction as defined by:

    • Myocardial infarction within the last 3 months of study entry, or
    • Reduced left ventricular function with an ejection fraction < 50% as measured by echocardiogram (will only be performed when clinically suspected) or
    • Unstable angina or
    • New York Heart Association (NYHA) grade III or IV congestive heart failure (see appendix C) or
    • Severe cardiac arrhythmias
  10. Age 75 years or older.
  11. Known intolerance to any of the chemotherapeutic drugs in the protocol.
  12. Positive pregnancy test.
  13. Lactating female or female of childbearing potential not using adequate contraception.
  14. Known inherited bone marrow failure syndromes (e.g., Fanconi anemia, Dyskeratosis congenita and related telomeropathies (e.g., TERT, TERC, DKC1 mutations).
  15. Patients with a history of non-compliance to medical regimens or who are considered unreliable with respect to compliance.

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: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
実験的:Hydroxyurea added to fludarabine, ara-C, idarubicin and venetoclax
Hydroxyurea 500-1000 mg administered 1 hour before each infusion of cytarabine.
他の名前:
  • ヒドロキシウレア

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
1-year EFS
時間枠:From initiation of study treatment to the first occurrence of treatment failure, hematologic relapse after CR/CRi, or death from any cause, whichever occurs first, assessed up to 365 days.
Defined as event-free-survial from the time from initiation of study treatment to the first occurrence of treatment failure, hematologic relapse from CR/CRi, or death from any cause.
From initiation of study treatment to the first occurrence of treatment failure, hematologic relapse after CR/CRi, or death from any cause, whichever occurs first, assessed up to 365 days.

二次結果の測定

結果測定
メジャーの説明
時間枠
Safety and tolerability: incidence and severity of treatment-emergent adverse events
時間枠:From registration in the study until 60 days after the last dose of treatment.
Frequency, nature and severity of non-hematological toxicities, including potential ara-C or fludarabine related neurological or dermatological adverse events.
From registration in the study until 60 days after the last dose of treatment.
Overall survival (OS)
時間枠:From initiation of study treatment through 2 years of follow-up.
Overall survival (OS), defined as the time from initiation of study treatment to death from any cause, with survival estimates reported at 1 and 2 years after initiation of study treatment.
From initiation of study treatment through 2 years of follow-up.
2-year event-free survival (EFS)
時間枠:From initiation of study treatment through 2 years of follow-up.
Time from initiation of study treatment to the first occurrence of treatment failure, hematologic relapse after CR/CRi, or death from any cause, whichever occurs first.
From initiation of study treatment through 2 years of follow-up.
Relapse-free survival (RFS)
時間枠:From initiation of study treatment through 2 years of follow-up.
Overall survival (OS), defined as the time from initiation of study treatment to the date of death from any cause or hematologic relapse from CR/CRi, with survival estimates reported at 1 and 2 years after initiation of study treatment.
From initiation of study treatment through 2 years of follow-up.
Cumulative incidence of hematologic relapse
時間枠:From initiation of study treatment through 2 years of follow-up.
Cumulative incidence of hematologic relapse after achievement of CR/CRi, reported at 1 and 2 years. Death without prior relapse will be treated as a competing risk.
From initiation of study treatment through 2 years of follow-up.
Response rate
時間枠:At response assessment after Cycle 1 (between Day 25 and Day 35 from the start of Cycle 1).
Proportion of patients achieving complete remission (CR), complete remission with incomplete hematologic recovery (CRi), morphologic leukemia-free state (MLFS), partial remission (PR) and minimal residual disease (MRD) negativity.
At response assessment after Cycle 1 (between Day 25 and Day 35 from the start of Cycle 1).
Time to hematopoietic recovery
時間枠:From the start of each treatment cycle until hematopoietic recovery. Treatment cycles are of variable duration, with no predefined cycle length; the subsequent cycle is initiated only after hematopoietic recovery.
Time to hematopoietic recovery (ANC 0.5 and 1.0 x 109/L; platelets 50 and 100 x 109/L) after each chemotherapy treatment cycle, defined as the time from the start of the cycle until recovery.
From the start of each treatment cycle until hematopoietic recovery. Treatment cycles are of variable duration, with no predefined cycle length; the subsequent cycle is initiated only after hematopoietic recovery.
Rate of patients bridged to allo-HCT
時間枠:From treatment initiation until allogeneic hematopoietic cell transplantation, relapse/progression, death, or 2 years of follow-up, whichever occurs first.
Proportion of patients undergoing allogeneic hematopoietic cell transplantation.
From treatment initiation until allogeneic hematopoietic cell transplantation, relapse/progression, death, or 2 years of follow-up, whichever occurs first.
Early mortality (30-day and 60-day mortality)
時間枠:30 and 60 days after initiation of study treatment.
Proportion of patients who die from any cause within 30 and 60 days after initiation of study treatment.
30 and 60 days after initiation of study treatment.

その他の成果指標

結果測定
メジャーの説明
時間枠
Intracellular accumulation of ara-CTP and F-ara-ATP
時間枠:During the first 2 days of treatment (run-in phase), at 4 predefined time points.
Assessment of intracellular accumulation of ara-CTP and F-ara-ATP in circulating blasts as a biomarker for efficacy of added hydroxyurea.
During the first 2 days of treatment (run-in phase), at 4 predefined time points.
SAMHD1 protein expression
時間枠:At baseline, prior to initiation of study treatment.
Assessment of SAMHD1 protein expression in blasts before treatment as a biomarker for efficacy of added hydroxyurea
At baseline, prior to initiation of study treatment.

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

捜査官

  • 主任研究者:Christer C Nilsson, MD PhD、Karolinska University Hospital

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 (推定)

2026年10月1日

一次修了 (推定)

2029年6月1日

研究の完了 (推定)

2034年9月1日

試験登録日

最初に提出

2026年6月12日

QC基準を満たした最初の提出物

2026年8月11日

最初の投稿 (実際)

2026年8月17日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月17日

QC基準を満たした最後の更新が送信されました

2026年8月11日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • FLAsH-IV-AML

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?

いいえ

IPD プランの説明

IPD Sharing Statement: Individual participant data (IPD) will not be shared.

Justification: The study is an early-phase investigator-initiated clinical trial in a rare and high-risk patient population. Due to the small sample size, detailed molecular data, and potential risk of re-identification despite de-identification, individual participant data will not be made publicly available.

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

いいえ

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

いいえ

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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