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NCT00244231
A Placebo-Controlled, Double Blind Study to Evaluate the Efficacy and Safety of Nidadd in the Management of Hyperlipidemia
Phase 3 trial testing Nidadd in Hyperlipidemia in 70 participants. Completed in 1 August 2005.
Quick facts
| Lead sponsor | Genovate Biotechnology Co., Ltd., |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 70 |
| Start date | 1 October 2003 |
| Estimated completion | 1 August 2005 |
Drugs / interventions tested
- Nidadd — full drug profile →
Conditions studied
- Hyperlipidemia — all drugs for Hyperlipidemia →
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.
- Change from baseline in HDL-c levels
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):
-
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:
- PubMed search for NCT00244231
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Genovate Biotechnology Co., Ltd., trials
Trials by the same sponsor.
- NCT06167265 — BE Study of Once Daily PMR Compared to Twice Daily Cilostazol Tablets in Healthy Volunteers · Phase 1 · completed
- NCT05466734 — BE Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers · Phase 1 · completed
- NCT05191862 — Bioequivalence Study of PMR Compared to Cilostazol IR Tablets in Healthy Volunteers · Phase 1 · terminated
- NCT03864666 — Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers · Phase 1 · completed
- NCT03480321 — Pharmacokinetic Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00244231 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Genovate Biotechnology Co., Ltd.,
- Last refreshed: 27 February 2007
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