Last updated: 11/03/2018 21:04:46
This product has been transferred to Novartis. GSK Clinical Study Register is no longer maintained for this study. The most up to date information is available on clinicaltrials.gov.
A Non-randomized, Open-label, Phase II Study to Assess the Safety and Efficacy of Eltrombopag in Japanese Subjects with Refractory, Moderate or More Severe Aplastic Anemia
GSK study ID
200926
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
No longer a GSK study
No longer a GSK study
Trial overview
Official title: A Non-randomized, Open-label, Phase II Study to Assess the Safety and Efficacy of Eltrombopag in Japanese Subjects with Refractory, Moderate or More Severe Aplastic Anemia
Trial description: This is an open-label, non-randomized, phase II study to assess the efficacy and safety of eltrombopag in Japanese moderate or more severe aplastic anemia (AA) subjects with a platelet count <30,000/ microliter who are refractory to anti-thymocyte globulin (ATG)-based immunosuppressive therapy (IST), who have relapsed after ATG-based IST, or who are ineligible for ATG-based IST. Eltrombopag is expected to improve trilineage blood cells and decrease transfusion frequency based on the result from the previous study in patients with severe AA. This study will use the hematologic response rate, defined as the proportion of subjects showing improvement in at least one of the three blood cell lineages or a decrease in blood transfusion volume, as the primary endpoint. Twenty patients will be enrolled in the study. Treatment with eltrombopag will be started at 25 milligram (mg)/day and increased by 25 mg/day every 2 weeks according to the platelet count up to 100 mg/day. Response assessment will be performed at 3 months after starting the study treatment (Week 13). Subjects in whom the treatment is assessed as effective will be continued with the study treatment. Subjects in whom the treatment is assessed as effective (when meeting any of the response criteria) at 6 months after starting the study treatment (Week 26) may enter the extension phase and continue the treatment with eltrombopag. The primary endpoint is the hematologic response rate at Week26.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
N\A
Primary outcomes:
Neutrophil count
Timeframe: Baseline to Week 26
Hemoglobin
Timeframe: Baseline to Week 26
Platelet count
Timeframe: Baseline to Week 26
Secondary outcomes:
Proportion of subjects with reduced volume of transfusion (platelet and RBC)
Timeframe: Up to 2.5 years
Pharmacokinetics (PK) of eltrombopag
Timeframe: Up to Week 26
Change in neutrophil count in the absence of G-CSF
Timeframe: Up to 2.5 years
Frequency and volume of transfusion (platelet and RBC)
Timeframe: Up to 2.5 years
Proportion of subjects who become transfusion independent
Timeframe: Up to 2.5 years
Time to hematologic response and duration (any response according to the response criteria for the primary endpoint)
Timeframe: Up to 2.5 years
Number and proportion of subjects with adverse events (AE)
Timeframe: Up to 2.5 years
Change in hemoglobin in the absence of RBC transfusion
Timeframe: Up to 2.5 years
Number and proportion of subjects with bleeding and severity of bleeding
Timeframe: Up to 2.5 years
Change in platelet count in the absence of platelet transfusion
Timeframe: Up to 2.5 years
Hematologic response in terms of the platelet count, hemoglobin level, and neutrophil count (any response according to the response criteria for the primary endpoint)
Timeframe: Week13
Interventions:
Drug: Eltrombopag 12.5 mg
Drug: Eltrombopag 25 mg
Enrollment:
21
Observational study model:
Not applicable
Primary completion date:
2015-10-09
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Cytopaenia
Product
eltrombopag
Collaborators
Not applicable
Study date(s)
July 2014 to December 2016
Type
Interventional
Phase
2/3
Participation criteria
Sex
Female & Male
Age
18 - 79 Year
Accepts healthy volunteers
none
- Subject has given written informed consent. If a subject is under 20 years, both the subject and the subject’s legally acceptable representative have to give informed consent.
- Japanese subjects aged >=18 and <80 years at the time of informed consent.
- Treatment with ATG in the past 12 months. Note: Subjects who are receiving cyclosporine or anabolic steroids (excluding danazol) at a stable dose may be enrolled if laboratory values are stable at screening.
- Congenital aplastic anemia (e.g., Fanconi anemia, congenital dyskeratosis)
Inclusion and exclusion criteria
Inclusion criteria:
- Subject has given written informed consent. If a subject is under 20 years, both the subject and the subject’s legally acceptable representative have to give informed consent.
- Japanese subjects aged >=18 and <80 years at the time of informed consent.
- Diagnosis of moderate (stage II) or more Aplastic Anemia (AA) with platelet count <30,000/microliter (based on the diagnosis criteria of AA established by the Study Group on Idiopathic Hematopoietic Disorder as a part of Research on Measures for Intractable Diseases supported by Health and Labor Science Research Grants).
- Subjects who became refractory to Anti-thymocyte globulin (ATG)-based Immunosuppressive therapy (IST), who have relapsed after ATG-based IST, or who are ineligible for ATG-based IST. Note: Refractory or relapsed subjects to whom re-treatment with ATG is indicated should not be enrolled in the study. Subjects who have a sibling donor with matched human leukocyte antigen (HLA) should not be enrolled in the study. However, such subjects may be enrolled if the disease relapsed after hematopoietic stem cell transplantation (HSCT), if HSCT is not indicated, or the subject does not want to undergo HSCT.
- Adequate organ function at screening and Day 1 as defined as follows: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <=3 × central laboratory upper limit of normal (ULN); Creatinine, total bilirubin, and alkaline phosphatase (ALP) <1.5 × central laboratory ULN (total bilirubin <2.5 × central laboratory ULN with Gilbert's Syndrome)
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS): 0 or 1
- Subjects with QT interval corrected for heart rate by Fridericia’s formula (QTcF) <450 milliseconds (msec) or QTcF<480 msec with branch block. Corrected QT interval duration (QTc) is QT interval corrected by Fridericia formula (QTcF), machine or manual over read. QTcF is based on single or averaged QTc value of triplicate electrocardiogram (ECG).
- Subjects who meet one of the following conditions: Male subjects who have a female partner of childbearing potential must either have a prior vasectomy or agree to use an acceptable contraception from time of enrollment in the study until 16 weeks after the last dose of eltrombopag (based upon the lifecycle of sperm); Female subjects of non-childbearing potential (who are physiologically unable to become pregnant) defined as: Premenopausal women with documented bilateral oophorectomy, bilateral tubal ligation, or hysterectomy; or postmenopausal women after at least 12 months of natural amenorrhea [if uncertain, postmenopausal state should be confirmed by hematology result of follicle stimulating hormone (FSH) >40 milli international unit /milliliter (mIU/mL) or estradiol <40 picogram (pg)/mL (<140 picomole /Liter (pmoll/L)].; Female subjects of childbearing potential: Defined as those not meeting the definition of non-childbearing potential. Female subjects of childbearing potential must have a negative serum human chorionic gonadotropin (hCG) or urine pregnancy test within 7 days prior to the first dose of study treatment. It is recommended that the pregnancy test should be performed as close as possible to the first dose of study treatment. Female subjects with a positive pregnancy test must be excluded from the study. Subjects with a negative pregnancy test must use acceptable contraception including abstinence after the pregnancy test. Subjects must agree to use the acceptable contraception including abstinence from 14 days prior to the first dose of study treatment until 28 days after the last dose of eltrombopag.
Exclusion criteria:
- Treatment with ATG in the past 12 months. Note: Subjects who are receiving cyclosporine or anabolic steroids (excluding danazol) at a stable dose may be enrolled if laboratory values are stable at screening.
- Congenital aplastic anemia (e.g., Fanconi anemia, congenital dyskeratosis)
- Paroxysmal nocturnal hemoglobinuria (PNH) granulocyte clone size determined by flow cytometry >=50%
- Presence of chromosomal aberration (-7/7q- detected by fluorescence in situ hybridization (FISH), or other aberrations detected by Giemsa (G)-band staining) Note: Subjects with the result by G-band staining (bone marrow aspiration) not adopted into the abnormal clone definition of An International System for Human Cytogenetic Nomenclature (ISCN) can be enrolled as no chromosomal aberration.
- Past history of thromboembolism or current use of anticoagulants. Note: Subjects with antiphospholipid antibody syndrome (APS) should not be enrolled.
- Past or current history of malignant tumor. Note: Subjects who have a history of completely resected malignant tumor and have been disease-free for 5 years are eligible.
- Subjects who test positive for hepatitis B surface (HBs) antigen, hepatitis C virus (HCV) antibody, or human immunodeficiency virus (HIV) antibody at screening. Note: Subjects with inactive hepatitis B may be enrolled. Judgment of inactive hepatitis B will be done by GSK medical monitor.
- Subjects with concurrent uncontrollable severe infection (e.g., sepsis)
- Hepatic cirrhosis
- Cardiac disorder (congestive heart disease of New York Heart Association (NYHA) functional classification Grade II/III/IV), or arrhythmia with a risk of thrombosis (e.g., atrial fibrillation). Note: Subjects with NYHA Grade II due to cardiac disorder should not be enrolled but those with NYHA Grade II due to Aplastic Anemia (AA) may be enrolled.
- Alcohol or drug abuse
- Pregnant women (a positive serum or urine pregnancy test within 7 days prior to the first dose of study treatment) or lactating women. Note: Female subjects who are lactating are eligible to participate if they discontinue nursing prior to the first dose of study treatment and refrain from nursing until 5 days after the treatment completion.
- Past history of immediate or delayed hypersensitivity to compounds chemically similar to eltrombopag or their activators
- Treatment with another investigational product within 30 days or the period 5-fold longer than the half-life of the investigational product, whichever longer, prior to the first dose of eltrombopag
- Prior treatment with eltrombopag, romiplostim, or any other Thrombopoietin (TPO) receptor agonist
- Use of prohibited concomitant medications.
Trial location(s)
No location data available.
Study documents
No study documents available.
Results overview
Study Results yet to be posted
Recruitment status
No longer a GSK study
Actual primary completion date
2015-10-09
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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