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trial · primary record

1 tablet of Prenofitol

Dyslipidemia

PhasePhase 2
StatusRECRUITING
SponsorUnknown
Enrolment160
Primary completion2027-12-31
Primary endpointThe proportion of patients achieving the target LDL-C level of <3.0 mmol/L compared with the baseline value in the investigational treatment groups and the placebo group at 90 days from the start of treatment (Visit 8).
Registry IDNCT07908433

Provenance

  • Source: ClinicalTrials.gov
  • Fetched at: 2026-11-02T15:42:53.559Z
  • Licence class: attribution-required
  • Verdict: primary-source
  • Entity id: NCT07908433

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