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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)

11. August 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

26

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

      • Stockholm, Schweden
        • Medical Unit Hematology, Karolinska University Hospital
        • Kontakt:
        • Hauptermittler:
          • Christer C Nilsson, MD PhD

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Hydroxyurea added to fludarabine, ara-C, idarubicin and venetoclax
Hydroxyurea 500-1000 mg administered 1 hour before each infusion of cytarabine.
Andere Namen:
  • Hydroxyharnstoff

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
1-year EFS
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Safety and tolerability: incidence and severity of treatment-emergent adverse events
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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.

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Intracellular accumulation of ara-CTP and F-ara-ATP
Zeitfenster: 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
Zeitfenster: 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.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Christer C Nilsson, MD PhD, Karolinska University Hospital

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Oktober 2026

Primärer Abschluss (Geschätzt)

1. Juni 2029

Studienabschluss (Geschätzt)

1. September 2034

Studienanmeldedaten

Zuerst eingereicht

12. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. August 2026

Zuerst gepostet (Tatsächlich)

17. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

17. August 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. August 2026

Zuletzt verifiziert

1. August 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • FLAsH-IV-AML

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

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