Beta Thalassemia Major AnemiaMyelodysplastic Syndrome
Investigational drug(s) / intervention(s)
SP-420
SP-420: Capsules for oral intake
Study summary
The goal of this clinical trial is to learn about SP-420 ability to remove iron from organs in subjects with transfusion-dependent β-thalassemia or transfusion-dependent low-risk myelodysplastic syndrome.
The main questions it aims to answer are:
* How efficient is SP-420 in cleaning iron from the liver?
* How is the safety and tolerability of ascending doses of SP-420?
Participants will:
* Take medication three times weekly
* Attend up to 20 site visits
* Undergo MRI scans
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Thalassemia cohorts:
Inclusion criteria:
* Women and men aged 18 years or older
* Transfusion-dependent β-thalassemia including HbE/β-thalassemia requiring iron chelation therapy (β-thalassemia with mutation and/or multiplication of α-globin is allowed)
* On a stable dose of iron chelation for at least 4 weeks prior to screening
* Weight ≥ 35kg at screening
* Transfusion iron overload
* Treated and followed for at least the past 6 months in a specialized centre
Exclusion criteria:
* β-thalassemia with the structural Hb variants HbS and HbC
* Current MDS
* Current biliary disorder
* Historic or ongoing clinically significant kidney disease
* Unable to undergo trial assessments including MRI e.g. due to claustrophobia in MRI scanner
* Pregnant or nursing women
* Men who do not agree to practice effective barrier contraception during the entire period
Myelodysplastic Syndromes Cohorts:
Inclusion criteria:
* Women and men aged 18 years or older
* Very low, low, or intermediate risk Myelodysplastic Syndrome according to IPSS-R
* Weight ≥ 35kg at screening
* Transfusion iron overload
* Treated and followed for at least the past 6 months at medical facilities experienced with MDS
Exclusion criteria:
* Therapy-related MDS or MDS with a known bone marrow fibrosis
* Diagnosis of decompensated liver cirrhosis
* Clinically significant kidney disease, either historic or ongoing
* Uncontrolled ischemic heart disease or uncontrolled arrythmia
* Uncontrolled hypertension
* Uncontrolled dyslipidaemia
* Uncontrolled Diabetes
* Major surgery within 8 weeks prior to screening
* Pregnant or nursing women
* Men who do not agree to practice effective barrier contraception during the entire period
Primary outcome measure(s)
To establish dose-response relationship of SP-420 for 24 weeks in the treatment of subjects with transfusion-dependent β-thalassemia — 24 weeks
To assess the safety and tolerability of ascending doses of SP-420 after 12 weeks treatment of subjects with transfusion-dependent low-risk myelodysplastic syndrome — 12 weeks
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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