An Open, Prospective, Single-arm Study of Olverembatinib Plus Venetoclax and Dexamethasone in Patients of Newly-diagnosed Ph+ Acute Lymphoblastic Leukemia
The purpose of this study is to explore the efficacy and safety of the OVD chemotherapy-free regimen (Olverembatinib, venetoclax and dexamethasone) in patients with newly-diagnosed Ph+ALL.
• Diagnosis of newly-diagnosed Ph+ acute lymphoblastic leukemia
• Age \>= 18
• Adequate hepatic function
• Adequate renal function
• Adequate heart function
• Life expectancy of more than 3 months
• Women of child-bearing potential and men with partners of child-bearing potential must agree to use 2 methods of birth control or be surgically sterile or abstain from heterosexual activity from the time of signing the informed consent for through 120 days after the last dose of study medication.
• Women of childbearing potential have negative pregnancy test within 72 hours of initiating study drug dosing.
• Male subjects must agree to use a latex condom during sexual contact with females of childbearing potential even if they have had a successful vasectomy starting with the first dose of study therapy through 120 days after the last dose of study therapy.
• All subjects must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure.
• Females of reproductive potential must adhere to the scheduled pregnancy testing as required in the POMALYST REMS program.