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NCT Number: NCT05445154

SKLB1028, Daunorubicin, and Cytarabine in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

The purpose of this study is to describe the dose limiting toxicities (DLT) of SKLB1028 when combined with cytarabine/ daunorubicin remission induction in a 7+3 schedule. Safety and tolerability of SKLB1028 will also be evaluated. This study will also characterize the pharmacokinetics (PK) of SKLB1028 when given in combination with cytarabine/daunorubicin remission induction and high-dose cytarabine (HiDAC) consolidation therapy in newly diagnosed acute myeloid leukemia .

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Key information

Age range

18 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

West China Hospital of Sichuan University

Chengdu, China

Location status: Recruiting

Location contact

Liu Ting, Chief doctor

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject has a diagnosis of previously-untreated de novo acute myeloid leukemia (AML) > 20% blasts in the bone marrow according to WHO classification (2016) documented prior to enrollment.;
  • Age ≥ 18 and < 60 years;
  • Subjects who are positive for FLT3 mutations by central laboratory;
  • Subject has an Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2;
  • Subject must meet the following criteria as indicated on the clinical laboratory tests;
  • Serum aspartate aminotransf
  • Total serum bilirubin ≤ 2.5 x institutional ULN
  • Serum creatinine ≤ 3 x institutional ULN or an estimated glomerular filtration rate (eGFR) of > 30 ml/min
  • Subject is suitable for oral administration of study drug.

Exclusion criteria

  • Confirmed diagnosis of acute promyelocytic leukemia (M3 /APL), or BCR-ABL positive leukemia (ie, blast crisis of chronic myelogenous leukemia);
  • Diagnosis of active malignancy other than AML;
  • AML secondary to radiotherapy or chemotherapy for other tumors;
  • AML with central nervous system involvement;
  • Refractory hypokalemia or hypomagnesemia that is not easily corrected by symptomatic treatment and that occurs repeatedly in the past;
  • Current clinically significant graft-ve
  • Previous history of other malignancies.
  • Patients with clinically significant coagulation abnormalities, such as disseminated intravascular coagulation (DIC), hemophilia A, hemophilia B, and von Willebrand disease;
  • Major surgery of major organs has been performed before entering the study (for the definition of major surgery, refer to Grade 3 and 4 surgery specified in Management Measures for Clinical Application of Medical Technology, or the patient has not yet fully recovered from
  • Subject has received prior therapy for AML with the following exceptions: a. emergency leukapheresis; b. emergency treatment with hydroxyurea ;c. growth factor or cytokine support; d. steroid for anaphylaxis or transfusion reaction;

Treatment and study plan

SKLB1028 Dose Escalation

Drug

Drug :SKLB1028 ;Drug: Cytarabine ;Drug: Daunorubicin

Primary outcomes

  1. Number of participants with dose limiting toxicities (DLTs)

    Time frame: up to Day42

    A DLT is defined as any Grade ≥ 3 non-hematologic or extramedullary toxicity that occur during the DLT assessment period, and that is considered to be possibly, probably, or definitely related to onsolidation therapies including the study drugs.

Secondary outcomes

  1. Pharmacokinetics profile of SKLB1028

    Time frame: Days 8, 15, 18, and 21 for remission induction and Days 8, and 21 for consolidation and Days 1 for maintenance

    Observed trough concentration (Ctrough)

  2. CR rate after the induction therapy

    Time frame: up to 3months

    CR is defined as a morphologically leukemia-free state at the post-baseline visit, having a neutrophil count of ≥ 1,000/mm^3 and platelet count of ≥ 100,000/mm^3, bone marrow blasts < 5%. There must be no evidence of Auer rods and no evidence of extramedullary leukemia.

  3. Duration of remission

    Time frame: up to 24months

    Duration of remission included duration of composite complete remission (CRc), duration of complete remission (CR)/ complete remission with partial hematologic recovery (CRh), duration of CRh, duration of CR and duration of response (CRc + partial remission (PR).

  4. Overall Survival

    Time frame: up to 60months

    OS was measured from the date of the first dose of treatment to the date of death from any cause or to the last date that the patient was known to be alive

  5. Event-Free Survival

    Time frame: up to 24months

    EFS was defined as the time from randomization until treatment failure (Composite complete remission (CRc) or partial remission (PR) were not reached within 4 cycles), relapse (excluding relapse after PR), or death from any cause, whichever occurs first.

  6. Leukemia-free survival

    Time frame: up to 24months

    The LFS was defined as the time from the date of first CR until the date of documented relapse (excluding relapse from PR) or death for participants who achieved CR (relapse date or death date - first CR disease assessment date + 1).

  7. Rate of hematopoietic stem cell transplantation

    Time frame: up to 12months

    Transplantation rate is defined as the percentage of participants undergoing hematopoietic stem cell transplant (HSCT).

Study contacts

Contact information is provided by the study sponsor or research team.

Liu Ting, Chief doctor

CONTACT

[email protected]

+8618980601240

Wang Jianxiang, Chief doctor

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

Industry

Registry information

Official study title

A Single-Arm, Multicenter, Open-Label, Dose- Escalating and Expanding,Phase I/II Study of SKLB1028 Combined With "7+3" Standard Chemotherapy in Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

Important dates

Study start
2021
Primary completion
2024
Study completion
2026
First posted
Jul 6, 2022
Registry last updated
Jul 6, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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