About this trial
To learn if the combination of blinatumomab and asciminib can help to control Ph+ ALL.
Eligibility criteria
Qualifiers
Performance status ≤2 (ECOG Scale) if age ≥18 years or Lansky ≥50 if age <18 years
Weight ≥40kg
Total serum bilirubin ≤ 2 x upper limit of normal (ULN), unless due to Gilbert's syndrome
Alanine aminotransferase (ALT) ≤ 3 x ULN, OR
Disqualifiers
Active serious infection not controlled by oral or intravenous antibiotics.
Active secondary malignancy other than skin cancer (e.g., basal cell carcinoma or squamous cell carcinoma) that in the investigator's opinion will shorten survival to less than 1 year.
Active Grade III-V cardiac failure as defined by the New York Heart Association Criteria.
Prolonged QTc interval on pre-entry electrocardiogram (> 470 msec) unless corrected after electrolyte replacement or approved by cardiologist
Trial design
Treatments tested in this trial
- Blinatumomab
- Asciminib
Treatment groups
Sponsors and collaborators
M.D. Anderson Cancer Center
Lead sponsor
Novartis Pharmaceuticals
Collaborator