Leukemia, Myelodysplastic Syndromes
Conditions
Keywords
Leukemia, Myelodysplastic Syndromes, Phase I
Brief summary
In this study, MGCD0103, a new anticancer drug under investigation, is given twice weekly to patients with leukemia or myelodysplastic syndromes.
Interventions
DRUGMGCD0103
MGCD0103 oral dose given 2 times per week.
Sponsors
Mirati Therapeutics Inc.
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients must have a diagnosis of one of the following: * relapsed or refractory AML or ALL that has failed to respond to standard therapy, has progressed despite standard therapy. * relapsed or refractory Myelodysplastic Syndromes including CMML (chronic myelomonocytic leukemia) or other myeloproliferative disorders provided there is an MDS component. * previously untreated AML or Myelodysplastic Syndromes in patients \>60 years of age who refused or are not candidates for induction chemotherapy * Patients with relapsed or refractory CML that has failed to respond to imatinib therapy or standard therapy, has progressed despite standard therapy, or for which no standard therapy exists. * ECOG performance status of 0, 1, or 2. * Age ≥18 years. * Laboratory requirements. * Patients or their legal representative must be able to read, understand, and sign a written informed consent (approved by the IRB/EC) prior to study entry.
Exclusion criteria
* Patients with other active malignancy except basal cell carcinoma or cervical intraepithelial neoplasia (CIN / cervical in situ). * Patients with suspicion of CNS involvement (tests are not required to rule out CNS involvement in the absence of signs or symptoms). * Pregnant or lactating women. Women of child-bearing potential must have a negative serum pregnancy test documented within 7 days prior to registration on study. * Patients and their partners, if either are of childbearing potential, not using adequate birth control measures throughout the course of the study. Both men and women enrolled on study must agree to use a medically acceptable effective form of contraception during the study and for 90 days following the last dose of study medication. An effective form of contraception is an oral contraceptive or a double barrier method, such as condom with diaphragm. * Patients with serious illnesses, medical conditions, or other medical history, including laboratory results, which, in the investigator's opinion, would be likely to interfere with a patient's participation in the study, or with the interpretation of the results. * Patients who have been treated with any investigational drug within 30 days prior to study initiation (an investigational drug is one for which there is no approved indication), or who are receiving concurrent treatment with other experimental drugs or anti-cancer therapy. * Known hypersensitivity to any of the components of MGCD0103. * Known HIV or Hepatitis B or C (tests do not need to be performed to rule out any of these infections). * Any psychiatric illness/social situations that would, in the judgment of the investigator, limit compliance with study requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety and tolerability. | 1 year (anticipated) |
Secondary
| Measure | Time frame |
|---|---|
| Clinical response. | 1 year (anticipated) |
| Dose limiting toxicities | 1 year (anticipated) |
| Pharmacokinetics | 1 year (anticipated) |
| Pharmacodynamics (histone acetylation, biomarkers) | 1 year (anticipated) |
Countries
Canada, United States
Outcome results
None listed