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NCT06220487RecruitingPhase 2

A Single-arm, Open-label Study of Olverembatinib, CD3/CD19 Bispecific T-cell Engager, and Chidamide in Patients With Newly Diagnosed Ph+ALL

A Single-arm, Open-label Study of Olverembatinib, CD3/CD19 Bispecific T-cell Engager, and Chidamide in Patients With Newly Diagnosed Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia

Source: ClinicalTrials.gov · Last updated 24 Jan 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

ABC study is a phase 2, single-arm, open-label study of Olverembatinib, CD3/CD19 Bispecific T-cell Engager, and Chidamide in patients with newly diagnosed Philadelphia Chromosome-positive acute lymphoblastic leukemia (Ph+ALL). This study combined third generation TKI (Olverembatinib), histone deacetylase inhibitors (Chidamide) and CD3/CD19 bispecific T-cell engager (Blinatumomab) as first line regimen (ABC regimen) for Ph+ ALL. Investigatorsaim to explore the efficacy and safety of ABC regimen. The primary endpoint is the complete molecular remission (CMR) at 3 months, secondary endpoints are overall survival (OS), event-free survival (EFS), adverse event (AE), IKZF1del, IKZF1plus, IKZF1lpus/CD20 subgroup EFS/OS.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
67 (estimated)
First submitted
3 Dec 2023
Start date
1 Feb 2024
Primary completion date
31 Dec 2025
Lead sponsor
Nanfang Hospital, Southern Medical University
NCT number
NCT06220487

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 67
  • From 1 Feb 2024 to the primary completion date, 31 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of receiving systemic chemotherapy or CAR-T therapy for ALL.

Other illness

  • Impaired cardiac function, including any one of the following:
  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of olverembatinib or chidamide (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection). .History of or current autoimmune disease. .History of or current relevant CNS pathology. .Presence of CNS leukemia. .History of or current autoimmune disease. .History of other malignancies. .Presence active infection.

Lab values

  • .LVEF \<45% as determined by MUGA scan or echocardiogram. .Complete left bundle branch block. .Use of a cardiac pacemaker.
  • ST depression of \>1mm in 2 or more leads and/or T wave inversions in 2 or more contiguous leads. .Congenital long QT syndrome. .History of or presence of significant ventricular or atrial arrhythmia. .Clinically significant resting bradycardia (\<50 beats per minute). .QTc \>450 msec on screening ECG (using the QTcF formula). .Right bundle branch block plus left anterior hemiblock, bifascicular block. .Myocardial infarction within 3 months prior to starting olverembatinib . .Angina pectoris.

Other

  • Nursing women or women of childbearing potential not willing to use an effective form of contraception during participation in the study and at least 3 months thereafter or male patients not willing to ensure effective contraception during participation in the study and at least three months thereafter.
  • Not eigiable for this study, decided by PI

Who the study is looking for

  • Signed written informed consent;
  • Newly diagnosed adult B-precursor Ph+ ALL;
  • Age greater or equal to 18 years;
  • ECOG Performance Status 0-1;
  • Ineligible for allo-HSCT.
  • Renal and hepatic function as defined below:
    • AST (GOT), ALT (GPT), and AP \<2 x upper limit of normal (ULN). Creatinine clearance equal or greater than 50 mL/min.
  • Pancreatic function as defined below:
    • Serum amylase less or equal to 1.5 x ULN Serum lipase less or equal to1.5 x ULN
  • Normal cardiac function;
  • Negative HIV test, negative HBV DNA and HCV RNA;
  • Negative pregnancy test in women of childbearing potential.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dept of Hematology, Nanfang Hospital, Southern Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.