| Protocol No: | ECCT/21/07/01 | Date of Protocol: | 22-09-2020 |
| Study Title: | A Phase 4, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy of Voxelotor for the Treatment of Leg Ulcers in Patients with Sickle Cell DiseaseA Phase 4, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy of Voxelotor for the Treatment of Leg Ulcers in Patients with Sickle Cell Disease |
| No Change | |
| Study Objectives: | Primary Objective The primary objective of this study is to assess the effect of voxelotor and SOC compared to placebo and SOC on leg ulcer healing in participants ≥ 12 years of age with SCD, as measured by the proportion of participants achieving resolution of target ulcer(s) in each treatment group by Week 12.
Secondary Objectives The secondary objectives of this study are to evaluate the effect of voxelotor and SOC compared to placebo and SOC on:
Exploratory Objectives The exploratory objectives will assess the effect of voxelotor and SOC compared to placebo and SOC (or open-label voxelotor and SOC, where applicable) on:
Safety Objective
The safety objective is to assess the safety and tolerability of voxelotor compared to placebo based on AEs, clinical laboratory tests, physical examinations, vital signs, and other clinical measures (eg, discontinuations due to AEs, dose reductions).
|
| 2 | Explorative objectives: Patient-Reported Outcome Measurements Information System (PROMIS) Pediatric Profile-37 v2.0/PROMIS-43 v2.1. |
| Laymans Summary: |
Sickle cell disease is an inherited blood abnormality caused by a change in the makeup of the Red blood cell forming genes that result in the clumping of the red cells. These
abnormal red cells tend to change shape and stick to each other and walls of blood vessels whenever they are exposed to low oxygen levels.
Persons with this gene abnormality experience several complications among them being leg ulcers because of damage of blood vessels. The prevalence of the leg ulcers
varies with geographical location and is estimated to be about 30% in Sub Sahara Africa among people with Sickle cell disease (SCD). No data on the prevalence of leg ulcers
in Kenya is available. There are no known effective treatments for leg ulcers in people with SCD. Current management is based on practice guidelines for treating other skin
ulcers which include use of dressings and application of medications on the ulcers and or surgical trimming and cleaning of the wounds.
Voxelotor is medicine that prevents the change on the shape of the red cells that causes clumping of the red cells. In the HOPE trial, though this was not among the main
study objectives, it was found that participants who had initially joined the study with leg ulcers experienced complete resolution of the ulcers and implies that voxelotor may
be useful in management of leg ulcers.
In this study, the effect of voxelotor on leg ulcer healing and safety will be studied in participants 12 years of age and older with SCD and active leg ulcer(s). Eighty (80)
participants will be recruited globally from the approximately 10 global sites. The primary objective of this study is to assess the effect of voxelotor and SOC compared to
placebo and SOC on leg ulcer healing in participants ≥ 12 years of age with SCD. The secondary objectives of this study are to evaluate the effect of voxelotor and SOC
compared to placebo and SOC on: • Time to healing of target ulcer(s) • Change in total surface area(s) of target ulcer(s), incidence of new ulcers. The primary outcome will be
measured by the proportion of participants achieving healing of the target ulcer(s). Exploratory outcomes will be summarized by descriptive statistics. Safety Analysis will be
performed on all participants receiving at least 1 dose of study drug.
|
| 2 | No Change |
| Abstract of Study: |
Sickle cell disease (SCD) is an inherited blood disorder caused by a point mutation in the β globin gene resulting in the formation of “sickle hemoglobin” (HbS), which
polymerizes in the deoxygenated state and leads to red blood cell (RBC) sickling.
Leg ulcers are a common complication of SCD, particularly among individuals with the more severe genotypes. Global prevalence of leg ulcers in the SCD population varies
geographically, with estimates of 14% to 18% in the United States (US) and Europe, 10% to 30% in sub-Saharan Africa, and 30% to 40% in Jamaica and Brazil. There is a large
unmet need for effective treatment for leg ulcers. In a Cochrane review of 5 randomized trials of interventions for treating leg ulcers in patients with SCD, none of the
therapies resulted in complete ulcer healing (Marti-Carvajal, 2014). Current management of SCD leg ulcers relies primarily on the practice approach used for other cutaneous
ulcers, involving debridement, wet to dry dressings, and topical agents.
Voxelotor (previously GBT440) is an HbS polymerization inhibitor that binds to HbS with a 1:1 stoichiometry and exhibits preferential partitioning to RBCs. The binding
increases HbS-oxygen (O2) affinity, stabilizing the oxyhemoglobin (oxyHb) state and inhibiting polymerization. Findings from the HOPE trial (study GBT440-031) suggest that
voxelotor may be an effective treatment for leg ulcers.
The effect of voxelotor on leg ulcer healing and safety will be assessed in participants 12 years of age and older with SCD and active leg ulcer(s) in this study. The study will
be conducted in approximately 80 eligible participants at approximately 10 global clinical trial sites. In our site we plan to recruit at least 20 patients. The primary objective of
this study is to assess the effect of voxelotor and SOC compared to placebo and SOC on leg ulcer healing in participants ≥ 12 years of age with SCD. The secondary objectives
of this study are to evaluate the effect of voxelotor and SOC compared to placebo and SOC on • Time to resolution of target ulcer(s) • Change in total surface area(s) of
target ulcer(s) • Incidence of new ulcers. The proportion of participants achieving resolution of the target ulcer will measure the primary endpoint. The analysis will use a
Cochran-Mantel-Haenszel (CMH) test to compare voxelotor + SOC with placebo + SOC groups, stratified by target ulcer size and target ulcer duration. For the time to
resolution, a stratified log-rank test will be used to compare the treatment groups. A Cox regression model will be used to estimate the hazard ratio between voxelotor +SOC
and placebo + SOC groups, as appropriate. Exploratory endpoints will be summarized by descriptive statistics. Safety Analysis will be performed on all participants receiving
at least 1 dose of study drug.
|
| 2 | No Change |