A Voxelotor for Sickle Cell Anemia Patients at Highest Risk for Progression of Chronic Kidney Disease
A Pilot Study of Voxelotor for Sickle Cell Anemia Patients at Highest Risk for Progression of Chronic Kidney Disease
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Santosh Saraf, MD
- Phone Number: 312-996-5680
- Email: ssaraf@uic.edu)
Study Contact Backup
- Name: Charity Ball, RN
- Phone Number: 312-996-2937
- Email: chball@uic.edu
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60612
- University of Illinois
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria
- Documentation of SCA genotype (HbSS or HbSβ0-thalassemia) may be based on history of laboratory testing or must be confirmed by laboratory testing during screening
- Participants have had urine dipstick defined hemoglobinuria (positive for blood (+1 or higher) and ≤ 2 red blood cells per high power field) on 2 prior outpatient visits
- Participants with albuminuria (urine albumin ≥ 30 mg/g creatinine) and an eGFR ≥ 60 mL/min/1.73m2 calculated using the CKD-EPI equation on 2 prior outpatient visits
- Age ≥18 years
- Hemoglobin (Hb) ≥ 5.5 and ≤ 10.0 g/dL during screening
- For participants taking hydroxyurea (HU), the dose of HU (mg/kg) must be stable for at least 90 days prior to signing the ICF and with no anticipated need for dose adjustments or initiation during the study, in the opinion of the Investigator
- Endari stable dose for one month.
- For participants taking an angiotensin converting enzyme (ACE)-inhibitor or angiotensin receptor blocker, the dose must be stable for at least 90 days prior to signing the ICF and with no anticipated need for dose adjustments or initiation during the study, in the opinion of the Investigator
- Participants, who if female and of child bearing potential, are using highly effective methods of contraception from study start to 30 days after the last dose of study drug, and who if male are willing to use barrier methods of contraception, from study start to 30 days after the last dose of study drug
- Participant has provided documented informed consent (the informed consent form [ICF] must be reviewed and signed by each participant
Exclusion Criteria
- Female who is breast feeding or pregnant
- Patients who are receiving regularly scheduled blood (RBC) transfusion therapy (also termed chronic, prophylactic, or preventive transfusion) or have received a RBC transfusion for any reason within 30 days of signing the ICF or at any time during the screening period
- Hospitalized for sickle cell crisis or other vaso-occlusive event within 14 days prior to signing the ICF (i.e., a vaso-occlusive event cannot be within 14 days prior to ICF)
- Hepatic dysfunction characterized by alanine aminotransferase (ALT) >4 × ULN
Participants with clinically significant bacterial, fungal, parasitic or viral infection which require therapy:
- Participants with acute bacterial infection requiring antibiotic use should delay screening/enrollment until the course of antibiotic therapy has been completed
- Participants with known active hepatitis A, B, or C or who are known to be human immunodeficiency virus (HIV) positive
- Severe renal dysfunction (estimated glomerular filtration rate at the Screening visit; calculated by the central laboratory) < 60mL/min/1.732, on chronic dialysis, or have received a kidney transplantation
- History of malignancy within the past 2 years prior to treatment Day 1 requiring chemotherapy and/or radiation (with the exception of local therapy for non-melanoma skin malignancy)
History of unstable or deteriorating cardiac or pulmonary disease within 6 months prior to consent including but not limited to the following:
- Unstable angina pectoris or myocardial infarction or elective coronary intervention
- Congestive heart failure requiring hospitalization
- Uncontrolled clinically significant arrhythmias
- Any condition affecting drug absorption, such as major surgery involving the stomach or small intestine (prior cholecystectomy is acceptable)
- Participated in another clinical trial of an investigational agent (or medical device) within 30 days or 5 half-lives of date of informed consent, whichever is longer, or is currently participating in another trial of an investigational agent (or medical device)
- Inadequate venous access as determined by the investigator/site staff
- Medical, psychological, or behavioral conditions, which, in the opinion of the Investigator, may preclude safe participation, confound study interpretation, interfere with compliance, or preclude informed consent
- Receipt of erythropoietin or other hematopoietic growth factors within 28 days of signing ICF or anticipated need for such agents during the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Voxelot
Voxelotor 1500mg once a day
|
Voxelotor 1500mg once a day
|
|
Other: Standard of Care (SOC)
Observational while receiving SOC
|
Voxelotor 1500mg once a day
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in albuminuria in voxelotor-treated SCA patients compared to the observation patients by a one-sided test
Time Frame: 48 weeks
|
Albuminuria will be analyzed comparing the mean values from the Week 47 and 48 visits to the mean values from the baseline and screening visits
|
48 weeks
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in albuminuria
Time Frame: 48 weeks
|
Proportion of subjects achieving a 25% decline in albuminuria in the voxelotor-treated group compared to the observation group
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in kidney function measure
Time Frame: 48 weeks
|
24 hour urine protein
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in In kidney function measure
Time Frame: 48 weeks
|
24 hour urine eGFR
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in kidney function measure
Time Frame: 48 weeks
|
24 hour urine albumin concentration
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in kidney function measure
Time Frame: 48 weeks
|
24 hour serum creatinine
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in Kidney function measure
Time Frame: 48 weeks
|
24 hour serum cystatin C
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in Kidney function measure
Time Frame: 48 weeks
|
24 hour serum BUN
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values in Kidney function measure
Time Frame: 48 weeks
|
CKD stage
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney function measure
Time Frame: 48 weeks
|
24 hour urine retinol binding protein
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney function measure
Time Frame: 48 weeks
|
24 hour urine β2 microglobulin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney function measure
Time Frame: 48 weeks
|
Plasma cell-free hemoglobin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney function measure
Time Frame: 48 weeks
|
Urine hemoglobin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney function measure
Time Frame: 48 weeks
|
Urine dipstick-defined hemoglobinuria)
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values markers of hemolysis
Time Frame: 48 weeks
|
Lactate dehydrogenase (LDH)
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values markers of hemolysis
Time Frame: 48 weeks
|
Aspartate aminotransferase (AST)
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values markers of hemolysis
Time Frame: 48 weeks
|
Indirect bilirubin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values markers of hemolysis
Time Frame: 48 weeks
|
Reticulocyte%
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values markers of hemolysis
Time Frame: 48 weeks
|
Hemoglobin concentration
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney injury biomarker
Time Frame: 48 weeks
|
Urine nephrin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney injury biomarker
Time Frame: 48 weeks
|
Urine podocalyxin
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney injury biomarker
Time Frame: 48weeks
|
Urine KIM-1
|
48weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values kidney injury biomarker
Time Frame: 48 weeks
|
Urine NGAL
|
48 weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values oxidative injury biomarker
Time Frame: 48weeks
|
Serum Methylenedioxyamphetamine (MDA)
|
48weeks
|
|
Change from the average of the Screening and Baseline values to the Week 47 and Week 48 values oxidative injury biomarker
Time Frame: 48 weeks
|
Serum 8-OHd
|
48 weeks
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Pathologic Processes
- Male Urogenital Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Chronic Disease
- Disease Attributes
- Genetic Diseases, Inborn
- Hematologic Diseases
- Renal Insufficiency
- Anemia, Hemolytic, Congenital
- Anemia, Hemolytic
- Anemia
- Hemoglobinopathies
- Anemia, Sickle Cell
- Kidney Diseases
- Renal Insufficiency, Chronic
Other Study ID Numbers
Other Study ID Numbers
- 2020-0047
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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