Olverembatinib Plus Venetoclax and Dexamethasone for Treatment-naïve Ph+ Acute Lymphoblastic Leukemia
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Olverembatinib plus venetoclax and dexamethasone.
- Who it may be relevant to
- Registry conditions: Newly-diagnosed Ph+ Acute Lymphoblastic Leukemia. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
An Open, Prospective, Single-arm Study of Olverembatinib Plus Venetoclax and Dexamethasone in Patients of Newly-diagnosed Ph+ Acute Lymphoblastic Leukemia
Overview
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.
Detailed description
PRIMARY OBJECTIVES:
To determine the Complete remission (CR) and complete remission with incomplete hematologic recovery (CRi) rates, the measurable residual disease (MRD) rates, the complete molecular remissions (CMR) rates and the progression-free survival (PFS) of the OVD chemotherapy-free regimen (Olverembatinib, venetoclax and dexamethasone) in patients with newly-diagnosed Ph+ALL.
SECONDARY OBJECTIVES:
To describe the toxicities of the OVD regimen. To assess the quality of life and overall survival of the OVD chemotherapy-free regimen in patients with newly-diagnosed Ph+ALL.
Interventions
- Drug Olverembatinib plus venetoclax and dexamethasone
Olverembatinib: orally every other day at a dose of 40mg Venetoclax: in a daily ramp-up strategy (100 mg d4, 200 mg d5, 400 mg d6-17) Dexamethasone: intravenously 10mg, d1-14, 5mg, d15-28
Primary outcome measures
- Complete remission (CR) and complete remission with incomplete hematologic recovery (CRi) rates [Time frame: Three years]
- Negative measurable residual disease (MRD) rates [Time frame: Three years]
- Complete molecular remissions (CMR) rates [Time frame: Three years]
- Progression-free survival (PFS) [Time frame: Three years]
Eligibility criteria
Inclusion criteria
- 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.
Exclusion criteria
- Current or anticipated use of other investigational agents.
- Female patients who are lactating or have a positive serum pregnancy test during the screening period.
- Major surgery within 3 weeks prior to first dose
- Acute active infection requiring systemic antibiotics, antivirals, or antifungals within two weeks prior to first dose
- Known or suspected HIV infection, known HIV seropositivity
- Active hepatitis infection
- Has known chronic obstructive pulmonary disease with a forced expiratory volume in 1 second (FEV1) <50% of predicted normal
- Known gastrointestinal disease or procedure that could interfere with the oral absorption or tolerance, including difficulty swallowing
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
China · 1 center
- Department of Hematology, Xijing Hospital, Fourth Military Medical University — Xi'an
Identifiers
NCT: NCT06082934 · 20232082