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Phase I trial of SAR103168, a novel multi-kinase inhibitor, in patients with refractory/relapsed acute leukemia or high-risk myelodysplastic syndrome.
- Source :
-
Leukemia & lymphoma [Leuk Lymphoma] 2015 Feb; Vol. 56 (2), pp. 395-400. - Publication Year :
- 2015
-
Abstract
- There is no effective treatment for relapsed/refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). We conducted a phase I dose escalation trial of SAR103168, a novel multi-targeted kinase inhibitor with activity against the Src kinase family, the BCR-Abl kinase and several angiogenic receptor kinases. Twenty-nine patients 18-83 years old were treated with SAR103168. Pharmacokinetics was characterized by plasma peak concentration (Cmax) at the end of the infusion, followed by a biphasic decline in the elimination profile. Adverse events were as expected for the patient population and there were no individual toxicities specific to SAR103168. Due to the unpredictable nature of drug exposure, the sponsor decided to discontinue the study prior to reaching the maximum tolerated dose.
- Subjects :
- Acute Disease
Adolescent
Adult
Aged
Aged, 80 and over
Area Under Curve
Dizziness chemically induced
Dose-Response Relationship, Drug
Drug Resistance, Neoplasm
Female
Humans
Hypokalemia chemically induced
Leukemia, Myeloid pathology
Male
Metabolic Clearance Rate
Middle Aged
Myelodysplastic Syndromes pathology
Neoplasm Recurrence, Local
Protein Kinase Inhibitors adverse effects
Protein Kinase Inhibitors pharmacokinetics
Protein Kinase Inhibitors therapeutic use
Pyridines adverse effects
Pyridines pharmacokinetics
Pyrimidines adverse effects
Pyrimidines pharmacokinetics
Risk Factors
Treatment Outcome
Young Adult
Leukemia, Myeloid drug therapy
Myelodysplastic Syndromes drug therapy
Pyridines therapeutic use
Pyrimidines therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1029-2403
- Volume :
- 56
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Leukemia & lymphoma
- Publication Type :
- Academic Journal
- Accession number :
- 24794806
- Full Text :
- https://doi.org/10.3109/10428194.2014.918970