A Study of Olverembatinib in the Treatment of Ph+ ALL

Philadelphia-Positive ALL Clinical Trial

Official title:

A Multicenter, Prospective Clinical Study of Olverembatinib Combined With Chemotherapy in the Treatment of de Novo Adult Philadelphia Chromosome-positive Acute Lymphoid Leukemia

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05466175
• Other study ID #: SZ-ALL01
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: October 1, 2022
• Est. completion date: September 30, 2024

Study information

• Verified date: July 2022
• Source: The First Affiliated Hospital of Soochow University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study, adults with newly-diagnosed Philadelphia Chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) will receive first-line therapy of a novel third-generation TKI Olverembatinib.

The main purpose of the study is to evaluate the efficacy and safety of Olverembatinib in Ph+ ALL patients.

Description:

Eligible participants will receive an 28-day induction regimen of Olverembatinib (40mg, QOD) combined with VP-chemotherapy, followed by 4 cycles of Hyper-CVAD A/B treatment (each lasting 28 days). If complete molecular response (CMR) is achieved at the 3rd month, participants will receive another three cycles of Hyper-CVAD A/B treatment. Maintenance therapy would be given for at least 1 year with monthly courses of vincristine, prednisone and Olverembatinib. If participants fail to achieve CMR at the 3rd month, or patients with an available matched donor had the option to proceed to allogeneic stem cell transplantation (allo-HSCT) at the discretion of the treating physician. Olverembatinib would be administered at the time of hematopoietic reconstruction for at least 1 year.

Intrathecal injection would be performed on day 15 of induction therapy and before each course of consolidation therapy to prevent central nervous system leukemia (CNSL).

It is expected that about 55 patients will take part in this study.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 55
• Est. completion date: September 30, 2024
• Est. primary completion date: September 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

1. Male or non-pregnant, non-lactating female patients who are 18 years of age or older.

2. Newly diagnosed Philadelphia chromosome-positive (Ph+) or BCR-ABL1-positive ALL, as defined by the 2016-WHO criteria. Participants should not be treated with any kind of TKIs or chemotherapy. Participants who only received preconditioning can be enrolled.

3. Eastern Cooperative Oncology Group (ECOG) performance status = 2, and expected survival period = 3 months.

4. Organ function as indicated by the following laboratory indicators must be met:

1) Alanine aminotransferase (ALT) = 2.5 × upper limit of normal (ULN), aspartate aminotransferase (AST) = 2.5 × ULN; 2) Total bilirubin=1.5×ULN; 3) Serum creatinine=1.5×ULN or 24-hour calculated creatinine clearance=50mL/min when serum creatinine >1.5×ULN; 4) Amylase=1.5×ULN, lipase=1.5×ULN; 5) Cardiac ejection fraction (EF) > 50%, pulmonary artery systolic blood pressure = 50mmHg; 6) QT interval corrected on electrocardiogram (ECG) evaluation: QTc=450ms in males or =470ms in females; 7) PT, APTT and INR=1.5×ULN.

5. Willingness and ability to comply with study procedures and follow-up examination.

Exclusion Criteria:

1. The presence of central nervous system (CNS) or testicular active ALL.

2. Human immunodeficiency virus (HIV) infection, or chronic infection with hepatitis B virus (HBsAg positive) or hepatitis C virus (anti-HCV positive).

3. Uncontrolled active infection.

4. Patients who are currently suffering from active autoimmune disease or a history of autoimmune disease potentially involving the CNS.

5. Patients who have a history of clinically significant CNS lesions or is currently suffering from clinically significant CNS lesions.

6. Patients who have any history of heart or vascular disease, such as hypertension (systolic blood pressure(HBP) > 140mmHg and/or diastolic blood pressure > 90mmHg), or take medications that are known to cause QT interval prolongation. The patients with well controlled HBP can be considered to be included.

7. Cardiac ultrasonography indicates that pulmonary artery systolic blood pressure is >50 mmHg; or there are clinical symptoms related to pulmonary arterial hypertension.

8. Patients who suffer from severe bleeding disorders unrelated to Ph+ ALL.

9. Patients who have any other malignant tumors that require treatment.

10. Patients who have a history of pancreatitis or a history of alcohol abuse.

11. Patients who have severe hypertriglyceridemia (triglyceride = 5.6mmol/L).

12. Patients who are pregnant, planning to become pregnant or breastfeeding.

13. Patients who underwent major surgery (except for minor surgery such as catheter placement or bone marrow biopsy) within 14 days before the first drug.

14. Patients who may not be able to complete all study visits or procedures required by the study protocol, including follow-up visits, and/or fail to comply with all required study procedures.

15. Patients who suffer from any condition or illness that, in the opinion of the Investigator, would compromise patient safety or interfere with the evaluation of the safety of the research drug.

Related Conditions & MeSH terms

• Philadelphia-Positive ALL

Intervention

Drug:
• Olverembatinib
Given PO
• Prednisone
Given Intravenous
• Vincristine
Given Intravenous

Locations

Country	Name	City	State
China	The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology	Suzhou	Jiangsu

Sponsors (1)

Lead Sponsor	Collaborator
Chen Suning

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants with Complete Molecular Remission	Will be estimated along with the 95% credible intervals.	From Induction through the end of one cycle of Hyper-CVAD A and B (approximately 3 months) (Cycle length is equal to [=] 28 days) ]
Secondary	Percentage of Participants with CR and Incomplete Complete Remission (CRi)	Will be estimated along with the 95% credible intervals.	At the end of consolidation therapy (approximately 9 months) and one year after allo-HSCT
Secondary	Duration of Complete Molecular Remission	Will be estimated along with the 95% credible intervals.	From the date of acquisition of complete molecular remission until the date of loss of complete molecular remission, assessed up to 2 to 4 years.
Secondary	Event-free survival (EFS)	The Kaplan-Meier method will be used to assess EFS probabilities.	From the first day of treatment until any failure (resistant disease, relapse, or death), assessed up to 2 to 4 years ]
Secondary	Overall survival (OS)	The Kaplan-Meier method will be used to assess OS probabilities.	From the first day of treatment to time of death from any cause, assessed up 2 to 4 years.
Secondary	Incidence of adverse events (AEs)	Will be graded according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5.0. The proportion of patients with AEs will be estimated, along with the Bayesian 95% credible interval.	Up to approximately 2 to 4 years