Clinical trial · Expanded Access
MAP to Provide Access to Nilotinib, for Patients With Relapsed or Refractory Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
Managed Access Program (MAP) to Provide Access to Nilotinib, for Patients With Relapsed or Refractory Philadelphia Chromosome Positive (Ph+) Acute Lymphoblastic Leukemia (ALL)
NCT04559555CI-TRIAL-00060210no longer availableClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this Cohort Treatment Plan is to allow access to nilotinib for eligible patients diagnosed with relapsed or refractory Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia (ALL).
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 |
|---|---|---|---|
| Acute Lymphoblastic Leukemia (ALL) | Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Nilotinib | Drug | Nilotinib | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: The following criteria must be fulfilled for the provision of Managed Access and will vary depending on the stage of the product lifecycle: * An independent request should be received from the Treating Physician (in some instances from Health Authorities, Institutions or Governments); * The patient to be treated has a serious or life threatening disease or condition, and no comparable or satisfactory alternative therapy is available to monitor or treat the disease or condition; * The patient is not eligible or able to enroll in a clinical trial; * There is a potential patient benefit to justify the potential risk of the treatment use, and the potential risk is not unreasonable in the context of the disease or condition to be treated; * Provision of the investigational product will not interfere with the initiation, conduct or completion of a Novartis clinical trial or overall development program and * Such access provision as described above is allowed as per local laws and regulations. Exclusion Criteria: Patients eligible for inclusion in this Treatment Plan have to meet all of the following criteria: 1. Male or Female patients age ≥ 18 years 2. WHO Performance Status of 0, 1 or 2 3. Relapsed or refractory Ph+ ALL 4. Imatinib (or dasatinib) must be discontinued at least 5 days prior to beginning therapy 5. Normal organ, electrolyte and marrow functions as described below: * Absolute Neutrophil Count (ANC) ≥ 1.0 x 1000000000/L * Platelets 50 x 1000000000/L * Potassium ≥ LLN (Lower limit of normal) or corrected to within normal limits with supplements prior to the first dose of nilotinib * Total calcium (corrected for serum albumin) ≥ LLN * Magnesium ≥ LLN or corrected to within normal limits with supplements prior to the first dose of nilotinib medication * AST and ALT ≤ 2.5 x ULN or ≤ 5.0 x UL:N if considered due to tumor * Alkaline phosphatase ≤ 2.5 x ULN * Serum bilirubin ≤ 1.5 x ULN * Serum amylase and lipase ≤ 1.5 x ULN
References
Publications (0)
Data not yet available
No reference posted for this study.