Active, not recruitingNot applicableNCT05791591

Safety and Efficacy of Orally Administered NUV001 Nutraceutical Supplement in Sickle Cell Disease Patients

Studying Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome

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Key facts

Sponsor
LGD
Principal Investigator
Matthias Canault, PhD
LGD
Intervention
NUV001 - IR(dietary_supplement)
Enrollment
168 target
Eligibility
18-65 years · All sexes
Timeline
20232024

Study locations (8)

Collaborators

ProRelix Research

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05791591 on ClinicalTrials.gov

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