A Study of Olverembatinib in Patients With Newly Diagnosed Ph+ALL.

Launched by ASCENTAGE PHARMA GROUP INC. · Sep 17, 2023

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called Olverembatinib for patients who have just been diagnosed with a specific type of leukemia known as Ph+ acute lymphoblastic leukemia (Ph+ ALL). The goal is to compare the effectiveness and safety of Olverembatinib combined with chemotherapy to another treatment called Imatinib, also used with chemotherapy. The trial is open to participants aged 65 and older, and it is currently recruiting patients from various locations around the world.

To be eligible for this study, participants must have a confirmed diagnosis of Ph+ ALL and be expected to live for at least three months. They should also be able to perform daily activities with some assistance, and their organs must be functioning well. Before joining, eligible participants will need to provide informed consent, meaning they understand the study and agree to take part. Throughout the study, participants will receive regular medical check-ups to monitor their health and the treatment's effects. It's important to note that certain medical conditions and medications may prevent someone from joining the trial, so potential participants should discuss their situation with their doctor.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Meet the WHO 2016 Ph chromosome or BCR/ABL1 positive Ph+ALL diagnostic and typing criteria for acute lymphoblastic leukemia. This is a newly diagnosed Ph+ALL.
• • 2. Expected survival of at least 3 months.
• • 3. ECOG ≤ 2.
• • 4. Adequate organ function.
• • 5. Use effective contraception during treatment and for at least three months after the last dose of the study drug, and male patients may not donate sperm.
• • 6. Pregnancy test results of serum samples obtained within 7 days prior to the first dosing of a fertile female subject were negative.
• • 7. Understand and voluntarily sign the informed consent approved by the Ethics Committee (EC) and voluntarily complete the study procedure and follow-up examination.
• Exclusion Criteria:
• • 1. A history of chronic myeloid leukemia and a diagnosis of acute leukemia with chronic myeloid leukemia.
• • 2. Clinical manifestations of central nervous system (CNS) leukemia or ALL extramedullary infiltration, except lymphadenopathy or hepatosplenomegaly.
• • 3. Previous or current clinical CNS diseases.
• • 4. Autoimmune diseases that may involve the CNS.
• • 5. Use therapeutic doses of anticoagulants and/or antiplatelet agents but allow low doses of anticoagulants to keep central venous lines open.
• • 6. Use a therapeutic drug that has drug interaction with the investigational drug due to other diseases within 7 days prior to the first receipt of the investigational drug.
• • 7. Uncontrolled Heart diseases.
• • 8. Had any VTE in the 6 months prior to randomization, including but not limited to deep vein thrombosis (DVT) or pulmonary embolism.
• • 9. Use of prohibited drugs.
• • 10. The presence of any disease or medical condition that is unstable or may affect its safety or compliance with the study.
• • 11. Medications known to cause prolonged QT interval.
• • 12. Active infections requiring systemic treatment.
• • 13. Disease that severely affects the oral administration and absorption of drugs, or an active gastrointestinal ulcer.
• • 14. Contraindications to the use of glucocorticoids, and the researchers judge that they are not suitable to participate in this study.
• • 15. Bleeding disorders unrelated to the tumor.
• • 16. Plan to undergone major surgery.
• • 17. Allergy to drug ingredients, excipients, or their analogues in the study.
• • 18. Female subjects who are pregnant or breastfeeding or expect to become pregnant during the study plan or within 3 months of the last dosing.
• • 19. Other malignant tumors within 2 years.
• • 20. Any symptom or illness that may interfere with the evaluation of the efficacy and safety of the investigational drug, or any other condition or condition that is not appropriate for participation in the study.