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Clinical Trials in Denmark / NCT05693909
Recruiting Phase 2

A Trial Testing SP-420 in Subjects With Transfusion-dependent β-thalassemia or Low-risk Myelodysplastic Syndromes

NCT05693909 · tracked via the Priya Life Science Denmark tracker
Phase
Phase 2
Started
2023-09-04
Last updated
2025-09-24

Condition(s) studied

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)

Trial sites (1)

FacilityCityRegionStatus
Pharmacosmos Investigational Site Copenhagen Denmark Recruiting

Other trials for the same condition

Official registry record

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.

View NCT05693909 on ClinicalTrials.gov ↗ ← All trials in Denmark