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NCT00244231

A Placebo-Controlled, Double Blind Study to Evaluate the Efficacy and Safety of Nidadd in the Management of Hyperlipidemia

Completed Phase 3 Last updated 27 February 2007
What this trial tests

Phase 3 trial testing Nidadd in Hyperlipidemia in 70 participants. Completed in 1 August 2005.

Timeline
1 October 2003
1 August 2005

Quick facts

Lead sponsorGenovate Biotechnology Co., Ltd.,
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment70
Start date1 October 2003
Estimated completion1 August 2005

Drugs / interventions tested

Conditions studied

Sponsor

Genovate Biotechnology Co., Ltd., — full company profile →

Who can join

Adults 20 to 75, any sex, with Hyperlipidemia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To assess the efficacy and safety of Nidadd (extended-release niacin) in patients with hyperlipidemia.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. NAD<sup>+</sup> metabolism: pathophysiologic mechanisms and therapeutic potential.
    Xie N, Zhang L, Gao W, Huang C, et al · · 2020 · cited 744× · PMID 33028824 · DOI 10.1038/s41392-020-00311-7

Verify or expand the search:

Other recruiting trials for Hyperlipidemia

Currently open trials in the same condition.

Other Genovate Biotechnology Co., Ltd., 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/NCT00244231.

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