Hematologic Malignancies
Conditions
Keywords
chronic lymphocytic leukemia, aggressive lymphoma, non-Hodgkin's lymphoma, Hodgkin's lymphoma, chronic myelogenous leukemia, multiple myeloma, acute lymphoblastic leukemia, acute myeloid leukemia
Brief summary
The purpose of this study is to characterize the safety and tolerability of repeat doses of compound GSK2110183 in subjects with hematologic cancer.
Interventions
DRUGGSK21110183
Starting Dose = 25mg once daily with dose escalation until unacceptable toxicity develops
Sponsors
Accenture
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Written informed consent is provided. 2. Male or female who is at least 18 years of age or older. 3. Histologically- or cytologically-confirmed diagnosis of a hematologic malignancy - that has relapsed or is refractory after standard therapy, AND that is not associated with human immunodeficiency virus (HIV) infection or solid organ transplant, including: * chronic lymphocytic leukemia (CLL), * chronic myelogenous leukemia (CML), * multiple myeloma (MM), * non-Hodgkin's lymphoma (NHL), * Hodgkin's lymphoma, or * Other hematologic malignancy excluding: * acute leukemia of any type * CML blast crisis * myelodysplastic syndrome (MDS) * myelofibrosis 4. Performance Status score of 0 and 1 according to the Eastern Cooperative Oncology Group (ECOG) scale 5. Able to swallow and retain oral medication. 6. Fasting serum glucose \< 126 mg/dL (\<7 mmol/L). 7. Male subjects with a female partner of childbearing potential must have had a prior vasectomy or agree to use adequate contraception from the time of the first dose of study drug until three months after the last dose of study drug. 8. A female subject is eligible to participate if she is of: * Non-childbearing potential * Child-bearing potential, has a negative serum pregnancy test during the screening period, and agrees to use adequate contraception from screening until four weeks after the last dose of study drug. 9. Adequate organ system function
Exclusion criteria
1. Chemotherapy, radiotherapy, or immunotherapy within 28 days (or 42 days for prior nitrosoureas or mitomycin C) prior to the first dose of study drug. 2. Use of an investigational anti-cancer drug within 28 days or five half-lives, whichever is longer, preceding the first dose of study drug. 3. Current use of a prohibited medication or requires any of these medications during treatment with study drug. 4. Current use of anticoagulants at therapeutic levels within seven days prior to the first dose of study drug, including warfarin, low molecular weight heparin and direct thrombin inhibitors. Low dose (prophylactic) anticoagulants are permitted provided that subject's PT and PTT meet entry criteria. 5. Current use of any anti-platelet agent (e.g. dipyridamole, clopidogrel) other than aspirin (81 mg daily). 6. Presence of active gastrointestinal disease or other condition that could affect gastrointestinal absorption (e.g. malabsorption syndrome) or predispose subject to gastrointestinal ulceration. 7. Any major surgery within the last four weeks. 8. Unresolved toxicity (except alopecia) Grade 2 from previous anti-cancer therapy unless agreed to by a Medical Monitor and the Investigator 9. Previously diagnosed diabetes mellitus (Type 1 or 2). 10. Current use of oral corticosteroids, with the exception of inhaled or topical corticosteroids. 11. Any serious or unstable pre-existing medical, psychiatric, or other condition (including lab abnormalities) that could interfere with subject safety or with obtaining informed consent. 12. Symptomatic or untreated central nervous system (CNS) involvement by the hematologic malignancy (including primary CNS lymphoma). 13. Evidence of severe or uncontrolled systemic diseases 14. Known infection with HIV, HBV or HCV. 15. QTc interval ≥ 470 msecs. 16. Other clinically significant ECG abnormalities including 2nd degree (Type II) or 3rd degree atrioventricular (AV) block. 17. History of myocardial infarction, acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting or bypass grafting within the past six months. 18. Class III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system. 19. Pregnant or lactating female. 20. Active drug or alcohol abuse. 21. History of sensitivity to heparin or heparin-induced thrombocytopenia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PK - oral clearance (CL/F) | Days -3, -2, -1, 8, 15 |
| Physical exam | Screening, Days -3, 8, At the start of each additional Cycle |
| Electrocardiogram (ECG) | Days -3, -2, -1, 8, 15, At the start of each additional Cycle |
| Vital signs | Screening, Days -3, -2, -1, 8, 15, At the start of each additional Cycle |
| Transthoracic Echocardiogram (TTE)/Multiple Gated Acquisition (MUGA) Scans | Screening, Additionally as needed |
| Clinical Laboratory assessments | Screening, Days -3, 1, 8, 15, At the start of each additional Cycle |
| ECOG Peformance Status | Screening, Days -3, 8, At the start of each additional Cycle |
| PK - Maximum observed plasma concentraion (Cmax) | Days -3, -2, -1, 8, 15 |
| PK - time to Cmax [tmax] (Maximum observed plasma concentration) | Days -3, -2, -1, 8, 15 |
| PK - Area under the plasma concentration-time curve (AUC(0-t)) | Days -3, -2, -1, 8, 15 |
| PK - Apparent terminal phase elimination rate constant | Days -3, -2, -1, 8, 15 |
| PK - Apparent terminal phase half-life (t1/2) | Days -3, -2, -1, 8, 15 |
Secondary
| Measure | Time frame |
|---|---|
| Metabolite Profiling | Days -3, 8 |
Countries
Australia, Canada, South Korea
Outcome results
None listed