Clinical trial

Use of Metformin as a Fetal Hemoglobin Inducer in Patients With Hemoglobinopathies

Name
H-38457 Metformin
Description
The purpose of this study is to determine whether metformin is effective in the treatment for sickle cell anemia (SCA).
Trial arms
Trial start
2017-03-02
Estimated PCD
2020-07-20
Trial end
2020-07-20
Status
Completed
Phase
Early phase I
Treatment
Metformin
Metfomin will be taken daily. The metformin dose will be increased during two time points per subject if protocol dose escalation criteria is met.
Arms:
Group A: Hydroxyurea + Metformin, Group B: Metformin (Group B has closed to enrollment)
Other names:
Glucophage, Riomet,
Questionnaires
Questionnaires will be completed to assess the impact quality of life
Arms:
Group A: Hydroxyurea + Metformin, Group B: Metformin (Group B has closed to enrollment)
Size
37
Primary endpoint
Change in Fetal Hemoglobin (HbF) Percentage (SCA) or Change in Total Hemoglobin (Hb)
1 Year
Eligibility criteria
Inclusion Criteria: 1. Confirmed diagnosis of sickle cell anemia 2. Age greater than or equal to 10 and less than or equal to 60 years of age. 3. If on hydroxyurea, fetal hemoglobin less than 20% at a stable dose (mg/kg) determined by the primary hematology provider over at least four months. 4. Creatinine less than or equal to 1.4 mg/dL and estimated glomerular filtration rate greater than 45 ml/min/1.73 m2 5. Liver function tests (specifically ALT and conjugated bilirubin) less than or equal to 4 times upper limits of normal. Exclusion Criteria: 1. Failure to meet inclusion criteria 2. Simple or chronic red blood cell transfusion therapy in the last 3 months OR a HbA level greater than 5% in SCA patients 3. Refusal to use medically effective birth control if female and sexually active. 4. If on hydroxyurea, not at stable dose of hydroxyurea for a minimum of 4 months (temporary exclusion). 5. Creatinine greater than 1.4mg/dL 6. Liver function tests (ALT and conjugated bilirubin) greater than 4 times upper limits of normal.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['EARLY_PHASE1'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 37, 'type': 'ACTUAL'}}
Updated at
2023-10-12

1 organization

1 drug

3 indications