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Actigraphy Improvement With Voxelotor (ActIVe) Study (ActIVe)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04400487
Recruitment Status : Not yet recruiting
First Posted : May 22, 2020
Last Update Posted : May 22, 2020
Sponsor:
Information provided by (Responsible Party):
Global Blood Therapeutics

Brief Summary:
This is a study to evaluate the effect of voxelotor on daily physical activity and sleep quality, as measured by a wrist-worn device in participants with sickle cell disease (SCD) and chronic moderate anemia.

Condition or disease Intervention/treatment Phase
Sickle Cell Disease Sickle Cell Anemia Drug: Voxelotor Phase 4

Detailed Description:

All participants will receive Voxelotor as treatment. There will be approximately 10 sites in the US.

Participant safety and tolerability will be monitored during the study using standard measures, including physical examinations, vital signs (including temperature, blood pressure, pulse rate, respiratory rate and peripheral oxygen saturation [SpO2]), clinical laboratory tests, and adverse event (AE) monitoring.

Screening Period (up to 4 weeks in duration): During this period, participants will sign the informed consent form (ICF), after which they will complete the screening assessments as detailed in the Schedule of Assessments (SOA).

Run-in Period (2 weeks in duration): During this period, participants will enter a 2-week run-in period (Day 14 to Day -1) during which baseline actigraphy measures of physical activity and sleep quality, overnight pulse oximetry assessments of oxygen saturation, and PRO assessments will be collected before initiating treatment with voxelotor.

Treatment Period (24 weeks in duration): After completion of the 14-day Run-in Period, participants will enter the open label treatment period and receive voxelotor 1500 mg once daily for 24 weeks. Repeat actigraphy assessments of physical activity and sleep quality, and overnight pulse oximetry will be performed during the treatment period (Weeks 10 to 12 and Weeks 22 to 24). PRO and Clinical Global Impression (CGI) assessments will be completed at scheduled study visits. The open-label treatment period is considered the continuous 24 weeks of voxelotor treatment from date of first dose (Day 1).

Follow-up Period (4 weeks in duration): Immediately following the 24-week treatment period, participants will enter a 4-week Follow-up Period.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 4, Multicenter, Open-label Study to Evaluate the Treatment Effect of Voxelotor on Physical Activity in Adolescents and Adults With Sickle Cell Disease
Estimated Study Start Date : June 2020
Estimated Primary Completion Date : September 2021
Estimated Study Completion Date : November 2021

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Voxelotor
Participants will receive voxelotor at 1500 mg
Drug: Voxelotor
500 mg Tablet, Oral, With or Without Food
Other Names:
  • GBT440
  • Oxbryta




Primary Outcome Measures :
  1. Change in total daily physical activity [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in total daily physical activity (expressed in counts per minute)

  2. Change in total nocturnal sleep time [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in total nocturnal sleep time (TST)

  3. Change in wake time after sleep onset [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in wake time after sleep onset (WASO)

  4. Change in sleep efficiency [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in sleep efficiency (SE) measured as total sleep time/time in bed

  5. Change in mean nocturnal hemoglobin oxygen saturation percentage [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in mean overnight SpO2 percentage as measured by pulse oximetry SpO2 percent

  6. Proportion of participants with a >1 g/dL increase in Hb [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Proportion of participants with a >1 g/dL increase in Hb

  7. Change in median number of overnight SpO2 dips > 3% per hour [ Time Frame: Baseline, Week 10-12, Week 22-24 ]
    Change in median number of overnight SpO2 dips > 3% per hour as measured by pulse oximetry SpO2 percent



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   12 Years to 55 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Male or female participants with SCA (sickle hemoglobin with two sickle cell genes [HbSS] or sickle hemoglobin (S) and one beta thalassemia gene [HbS β0] thal genotype)
  2. Between 12 to 55 years of age (inclusive)
  3. Screening Hb level <8.0 g/dL
  4. Treatment with hydroxyurea (HU) therapy on study is permitted if the participant has been on a stable dose for at least 90 days before enrollment with no dose modifications planned or anticipated by the Investigator
  5. Treatment with glutamine is permitted
  6. Treatment with erythropoiesis-stimulating agents (ESAs) is permitted if the participant has been on a stable dose for at least 12 weeks before enrollment with no dose modifications planned or anticipated by the Investigator
  7. Female participants of child-bearing potential must use highly effective methods of contraception to 30 days after the last dose of study drug. Male participants must use barrier methods of contraception to 30 days after the last dose of study drug
  8. Females of child-bearing potential are required to have a negative pregnancy test before the administration of study drug
  9. Written informed consent and/or parental/guardian consent and participant assent per Institutional Review Board (IRB) policy and requirements, consistent with ICH guidelines

Exclusion Criteria:

  1. Red blood cell (RBC transfusion within 3 months before initiation of study drug
  2. Planned initiation of regularly scheduled RBC transfusion therapy (also termed chronic, prophylactic, or preventive transfusion) during the study
  3. Hospitalization for vaso-occlusive crisis (VOC) or acute chest syndrome (ACS) within 30 days prior to informed consent/assent.
  4. More than 10 VOCs requiring hospitalization, emergency department or clinic visit within the past 12 months
  5. Planned elective surgery within the next 6 months
  6. Physical inactivity attributable to clinically significant musculoskeletal, cardiovascular, or respiratory comorbidities
  7. Anemia due to bone marrow failure (eg, myelodysplasia)
  8. Absolute reticulocyte count (ARC) < 100 x10^9/L
  9. Screening alanine aminotransferase (ALT) > 4× upper limit of normal (ULN)
  10. Severe renal dysfunction (estimated glomerular filtration rate [GFR] < 30 mL/min/1.73 m2 by Schwartz formula) or is on chronic dialysis
  11. Known active hepatitis A, B or C or known to be human immunodeficiency virus (HIV)-positive.
  12. Females who are breast-feeding or pregnant
  13. Major surgery within 8 weeks before enrollment. Participants must have completely recovered from any previous surgery before enrollment
  14. History of hematopoietic stem cell transplant or gene therapy
  15. Received an investigational drug within 30 days or 5-half-lives, whichever is longer, prior to consent, or is currently participating in another trial of an investigational or marketed drug (or medical device)
  16. Use of concomitant medications (eg, crizanlizumab) that confound the ability to interpret data from the study
  17. Medical, psychological, or behavioral condition that, in the opinion of the Investigator, would confound or interfere with evaluation of safety and/or efficacy of the study drug, prevent compliance with the study protocol; preclude informed consent; or, render the participant unable/unlikely to comply with the study procedures
  18. Use of herbal medications (e.g., St. John's Wort), sensitive cytochrome P450 (CYP) 3A4 substrates with a narrow therapeutic index, strong CYP3A4 inhibitors, fluconazole, or moderate or strong CYP3A4 inducers

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04400487


Contacts
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Contact: Carolyn Hoppe, MD 6507417741 choppe@gbt.com
Contact: David Tsai 4152654682 dtsai@gbt.com

Sponsors and Collaborators
Global Blood Therapeutics
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Responsible Party: Global Blood Therapeutics
ClinicalTrials.gov Identifier: NCT04400487    
Other Study ID Numbers: GBT440-039
First Posted: May 22, 2020    Key Record Dates
Last Update Posted: May 22, 2020
Last Verified: May 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Anemia, Sickle Cell
Anemia, Hemolytic, Congenital
Anemia, Hemolytic
Anemia
Hematologic Diseases
Hemoglobinopathies
Genetic Diseases, Inborn