West China Hospital of Sichuan University
Chengdu, China
Location status: Recruiting
Location contact
Liu Ting, Chief doctor
CONTACT
NCT Number: NCT05445154
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 .
Interested in participating?
Request Info18 year–59 year
All sexes
Interventional
Phase 1 / Phase 2
Chengdu, China
Location status: Recruiting
Liu Ting, Chief doctor
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Drug :SKLB1028 ;Drug: Cytarabine ;Drug: Daunorubicin
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.
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)
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.
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).
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
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.
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).
Time frame: up to 12months
Transplantation rate is defined as the percentage of participants undergoing hematopoietic stem cell transplant (HSCT).
Contact information is provided by the study sponsor or research team.
Liu Ting, Chief doctor
CONTACT
Wang Jianxiang, Chief doctor
CONTACT
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Industry
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)
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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