Last reviewed · How we verify

NCT05789355

Effect of NUV001 Supplementation in Patients Suffering From Sickle Cell Disease (SCD)

Active, enrolled NA Last updated 28 May 2024
What this trial tests

NA trial testing NUV001 in Sickle Cell Disease in 12 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 April 2023
Primary endpoint
10 May 2024
30 June 2024

Quick facts

Lead sponsorLGD
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment12
Start date1 April 2023
Primary completion10 May 2024
Estimated completion30 June 2024
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

LGD

Who can join

Adults 18 to 60, any sex, with Sickle Cell Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a pilot study of daily dosing of NUV001 as a dietary supplement in 12 sickle cell disease patients with 3 months of follow-up plus 1 month after supplementation.The present study is designed to evaluate, first, the safety and tolerability parameters as well as to measure the plasma and urinary residues of daily oral doses of NUV001. Secondly, the study will evaluate the impact of NUV001 on biological parameters and quality of life of patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Sickle Cell Disease

Currently open trials in the same condition.

Other LGD trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05789355.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing