Study of Decitabine and Tetrahydrouridine (THU) in Patients With Sickle Cell Disease

Sickle Cell Disease Clinical Trial

Official title:

Phase 1 Study of Oral Decitabine and Tetrahydrouridine (THU) in Patients With High Risk Sickle Cell Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01685515
• Other study ID #: CASE 10Z11
• Status: Completed
• Phase: Phase 1
• Start date: August 2012
• Est. completion date: June 2018

Study information

• Verified date: September 2018
• Source: The Cleveland Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purposes of this study are to observe if oral tetrahydrouridine and decitabine can increase fetal hemoglobin levels and improve the symptoms of sickle cell disease, and to monitor how patient's bodies react to oral tetrahydrouridine and decitabine.

Description:

The purposes of this study are to observe if oral tetrahydrouridine and decitabine can increase fetal hemoglobin levels and improve the symptoms of sickle cell disease, and to monitor how patient's bodies react to oral tetrahydrouridine and decitabine. The overall purpose is to develop disease modifying treatment for sickle cell disease that is less cytotoxic than the current standard of care, and which can directly and more efficiently reactivate fetal hemoglobin levels. The hypothesis is that patients treated with oral tetrahydrouridine and decitabine will have the same chance of severe non-hematologic toxicities as the placebo group. The primary end-point is ≥ grade 3 non-hematologic toxicity. The investigators' hypothesis is that patients in the treatment groups receiving oral THU-decitabine 2X/week over 8 weeks (n=15) will be equivalent to placebo group (n=10) with regards to the chance of ≥ grade 3 non-hematologic toxicity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: June 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age 18 years or older.

• Written, informed consent provided by the subject before study entry.

• Confirmed Sickle Cell Disease (SCD) (SS, S-b0-thalassemia, S-b+-thalassemia or SC on hemoglobin electrophoresis).

• Symptomatic SCD while on 6 months of HU OR symptomatic SCD and intolerant of HU (unable or unwilling to take HU due to hematological or other toxicities). Symptomatic SCD is defined as having one of following:

• Fetal Hemoglobin (HbF) <5%, OR

• 3 or more pain episodes per year requiring parenteral narcotics, OR

• 1 or more acute chest syndrome episodes, OR

• Hemoglobin <9 g/dL and absolute reticulocyte count <250,000/mm3.

• Subject is in his/her steady state and not amidst any acute complication due to SCD (i.e., hospitalization, acute pain, or acute chest syndrome in the past 14 days).

• Regular compliance with comprehensive care and previous therapy.

Exclusion Criteria:

• Inability to give informed consent.

• Experienced severe sepsis or septic shock within the previous 12 weeks.

• Last HU dose was ingested within the previous 4 weeks.

• Currently pregnant or breast-feeding.

• Alanine aminotransferase (ALT) greater than or equal to two times (2X) the upper limit of normal or albumin <2.0 mg/dL or direct (conjugated) bilirubin greater than or equal to 1.5 mg/dl.

• Serum creatinine >2.9 mg/dL and calculated creatinine clearance <30 mL/min.

• Platelet count >800 x 109/L.

• Absolute neutrophil count <1.5 x 109/L.

• Female of active childbearing potential who is unwilling to use at least one of the two following forms of birth control:

(i) not having heterosexual sexual contact beginning at the screening visit and continuing until 4 weeks after the last dose of THU-decitabine OR (ii) intrauterine device (IUD).

• Sexually active male who is unwilling to use a condom when engaging in any sexual contact with a female with child-bearing potential, beginning at the screening visit and continuing until 4 weeks after taking the last dose of THU-decitabine. This requirement applies also to males who have had a successful vasectomy.

• Altered mental status or recurrent seizures requiring anti-seizure medications.

• Moribund or any concurrent disease (e.g., hepatic, renal, cardiac, metabolic) of such severity that death within 24 weeks is likely.

• Concurrent diagnosis of malignancy including myelodysplastic syndromes (MDS), leukemia, or an abnormal karyotype.

• Vitamin-B12, folate, or iron deficient (until corrected).

• New York Heart Association (NYHA) class III/IV status.

• Eastern Co-operative Oncology Group (ECOG) performance status greater than or equal to 3.

• Participant is on chronic transfusion therapy (e.g., for history of Transient Ischemic Attack (TIA) or stroke) and medically contraindicated to discontinue transfusions (unless multiple allo-antibodies prevent the patient from getting transfusions as scheduled).

• Known history of illicit drug or alcohol abuse within the past 12 months.

• Other experimental or investigational drug therapy in the past 28 days.

Related Conditions & MeSH terms

• Anemia, Sickle Cell
• Sickle Cell Disease

Intervention

Drug:
• Oral Decitabine and Tetrahydrouridine
Oral Decitabine and Oral Tetrahydrouridine (THU) given 1-2 hours apart on 2 consecutive days over 8 weeks
• Placebo
Plain water will be dispensed at a similar volume and in the same containers as study drug. The water placebo has a similar appearance and taste to the study drug, since the study drug is highly diluted in water.

Locations

Country	Name	City	State
United States	University of Illinois at Chicago	Chicago	Illinois

Sponsors (2)

Lead Sponsor	Collaborator
Yogen Saunthararajah	University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Non-hematologic toxicity	Toxicities will be evaluated on a weekly basis and will be classified according to their grade and relationship to study treatment. Chi-square testing will be employed to examine the difference in number of patients with grade 3 or greater non-hematologic toxicity between treatment and placebo groups.	12 weeks