Clinical trial · Interventional
A Study Comparing Ponatinib and Nilotinib in Participants With Chronic Myeloid Leukemia
A Randomized, Open-label Study of Ponatinib Versus Nilotinib in Patients With Chronic Myeloid Leukemia in Chronic Phase Following Resistance to Imatinib
NCT02627677CI-TRIAL-00055243OPTIC-2LterminatedPhase 3Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The study was stopped due to operational feasibility and not due to any safety concerns
Summary
Brief summary (as posted)
The purpose of this study is to compare the efficacy and safety of 2 starting doses of ponatinib compared to nilotinib in participants with imatinib-resistant chronic myeloid leukemia (CML) in chronic phase (CP).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Chronic Phase Chronic Myeloid Leukemia | Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive | ALIAS | 0.90 |
Interventions
Interventions (3)
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Cohort A: Ponatinib 30 mg
- description
- Ponatinib 30 mg, tablets, orally, once daily (QD) until achievement of major molecular response (MMR) up to 12 months. Once MMR was achieved, participants received reduced dose of ponatinib 15 mg orally once daily up to 42 months.
- interventionNames
- Drug: Ponatinib 30 mg QD
- type
- EXPERIMENTAL
- label
- Cohort B: Ponatinib 15 mg
- description
- Ponatinib 15 mg, tablets, orally, QD until achievement of MMR up to 12 months. Once MMR was achieved, participants received reduced dose of ponatinib 15 mg orally once daily up to 45 months.
- interventionNames
- Drug: Ponatinib 15 mg QD
- type
- ACTIVE_COMPARATOR
- label
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Have CP-CML and are resistant to first-line imatinib treatment. 2. Be male or female ≥18 years old. 3. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 4. Have adequate renal function as defined by the following criterion: • Serum creatinine ≤1.5 × upper limit of normal (ULN) for institution. 5. Have adequate hepatic function as defined by all of the following criteria: * Total serum bilirubin ≤1.5 × ULN, unless due to Gilbert's syndrome * Alanine aminotransferase (ALT) ≤2.5 × ULN or ≤5 × ULN if leukemic infiltration of the liver is present * Aspartate aminotransferase (AST) ≤2.5 × ULN or ≤5 × ULN if leukemic infiltration of the liver is present. 6. Have normal pancreatic status as defined by the following criterion: * Serum lipase and amylase ≤1.5 × ULN. Exclusion Criteria: 1. Have previously been treated with any approved or investigational TKIs other than imatinib or treated with imatinib within 14 days prior to receiving study drug. 2. Have previously been treated with any anti-CML therapy other than hydroxyurea, including interferon, cytarabine, immunotherapy, or any cytotoxic chemotherapy, radiotherapy, or investigational therapy. 3. Underwent autologous or allogeneic stem cell transplant. 4. Are in CCyR or MMR. 5. Have clinically significant, uncontrolled, or active cardiovascular disease, specifically including, but not restricted to: * Any history of myocardial infarction (MI), unstable angina, cerebrovascular accident, or transient ischemic attack (TIA) * Any history of peripheral vascular infarction, including visceral infarction * Any history of a revascularization procedure, including vascular surgery or the placement of a stent * History of venous thromboembolism, including deep venous thrombosis, superficial venous thrombosis, or pulmonary embolism, within 6 months prior to enrollment * Congestive heart failure (New York Heart Association \[NYHA\] class III or IV) within 6 months prior to enrollment or left ventricular ejection fraction (LVEF) less than 45% or less than the institutional lower limit of normal (whichever is higher) within 6 months prior to enrollment.
References
Publications (0)
Data not yet available
No reference posted for this study.