Combination of Donafenib and Cytarabine/Daunorubicin in Relapsed AML

Acute Myeloid Leukemia (AML) Clinical Trial

Official title:

A Dose-escalated Phase Ⅰ Trial to Assess the Tolerance and Pharmacokinetics of Combination of Donafenib and Cytarabine/Daunorubicin in Relapsed AML Patient

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04402723
• Other study ID #: ZGDAML1
• Status: Terminated
• Phase: Phase 1
• Start date: November 6, 2018
• Est. completion date: February 9, 2022

Study information

• Verified date: November 2022
• Source: Suzhou Zelgen Biopharmaceuticals Co.,Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase Ⅰ study of Donafenib, an oral multikinase inhibitor that targets Raf kinase and receptor tyrosine kinases, is to assess safety and pharmacokinetics in patients with Relapsed AML.

Description:

Donafenib is a multikinase inhibitor which is acting on various cellular pathways involved in the genesis of acute myeloid leukemia (AML). Donafenib is therefore a promising candidate for improvement of chemotherapy results in AML. This clinical trial evaluates the safety and pharmacokinetics of Donafenib combination with Cytarabine/Daunorubicin for AML in patients between 18 and 55 years of age.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 8
• Est. completion date: February 9, 2022
• Est. primary completion date: February 9, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Patients with diagnosed AML (except APL) according to the FAB and WHO classification, including AML evolving from MDS or other hematologic diseases and AML after previous cytotoxic therapy or radiation (secondary AML) .

• Patients with diagnosed Relapsed AML according to Chinese Guidelines for the Diagnosis and Treatment of Acute Myeloid Leukemia.

• relapse after 6 months of an morphological remission.

• Age = 18 and = 55 years.

• BMI = 18 and =27.

• Informed consent, personally signed and dated to participate in the study.

• ECOG performance status of 0-1.

• Life expectancy of at least 12 weeks.

• Total serum bilirubin =1.5×ULN.

• Serum aspartate transaminase (AST) and/or alanine transaminase (ALT) = 2.5×ULN.

• Serum creatinine =1.5×ULN.

• glomerular filtration rate =60 mL/min, as calculated with the Cockcroft-Gault formula.

• alkaline phosphatase =1.5×ULN.

• urine protein =1+, or Urine protein was quantified for 24h =0.5g.

• INR/PTT <1.5×ULN.

Exclusion Criteria:

• Patients who are not eligible for standard chemotherapy as per discretion of the treating physician.

• Patients who have been treated with bone marrow transplantation.

• Central nervous system manifestation of AML.

• Cardiac disease: heart failure NYHA III or IV; unstable coronary artery disease (MI more than 6 months prior to study entry is permitted); serious cardiac ventricular arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted).

• Patients who have thrombosis events within 6 months prior to study entry is permitted.

• Pregnancy or breastfeed.

• Chronic pulmonary disease with relevant hypoxia.

• Patients undergoing dialysis.

• Known HIV and/or hepatitis C infection.

• Evidence or history of severe non-leukemia associated bleeding diathesis or coagulopathy.

• Evidence or recent history of CNS disease, including primary or metastatic brain tumors, seizure disorders.

• Blood pressure (BP) higher than systolic 140 mmHg and/or diastolic 90 mmHg after best treatment.

• Any severe concomitant condition which makes it undesirable for the patient to participate in the study or which could jeopardize compliance of the protocol.

• Patients with major surgery, open biopsy or significant traumatic injury within 4 weeks prior to study entry is permitted.

• Serious, non-healing wound, ulcer or bone fracture.

• Infection need antibiotic treatment.

• Cumulative therapeutic dose of Daunorubicin more than 300mg/m2.

• Concurrent malignancies other than AML.

• History of organ allograft.

• Allergy to study medication or excipients in study medication.

Related Conditions & MeSH terms

• Acute Myeloid Leukemia (AML)
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Donafenib
In first 28-days-cycle, eligible subjects will be given Donafenib 0.2/0.3g, bid, for first 14 days, combination with Daunorubicin 60mg/m2/d, for first 3 days, and Cytarabine 100mg/m2/d, for first 7 days. If CR or CRi is observed, subjects will be given Donafenib 0.2/0.3g, bid, for first 14 days, combination Cytarabine 2g/m2/q12h, for first 3 days, in next 28-day-cycle.

Locations

Country	Name	City	State
China	Institute of Hematology and Blood Disease Hospital	Tianjin	Tianjin

Sponsors (1)

Lead Sponsor	Collaborator
Suzhou Zelgen Biopharmaceuticals Co.,Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety(including the type, severity and frequency of AE)	Safety of combination of donafenib with Cytarabine/Daunorubicin in relapsed AML patients.	through study completion, an average of 2 months