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NCT02966028 · ClinicalTrials.gov registry record · Phase 2

Effect of SNF472 on Progression of Cardiovascular Calcification in End-Stage-Renal-Disease (ESRD) Patients on Hemodialysis (HD)

A Phase 2 study, sponsored by Sanifit Therapeutics S. A..

Completed
Registry status
Phase 2
Development phase
274
Enrollment target

NCT02966028: Completed Phase 2 study, sponsored by Sanifit Therapeutics S. A..

NCT02966028 is a Phase 2 study that has completed, run by Sanifit Therapeutics S. A.. The registered enrollment target is 274 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (106% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02966028, a Phase 2 study, has completed, sponsored by Sanifit Therapeutics S. A..

COMPLETED
Registry status
Phase 2
Development phase
274 participants
Enrollment target

Study Summary

The primary objective is to assess the effect of 2 dose levels of SNF472 (300 mg and 600 mg) compared to placebo on the progression of coronary artery calcium volume score over a 12-month (52 weeks) period in ESRD patients on HD

Primary Outcome

Coronary Artery Calcification (CAC) Volume Score is a calculation to quantify the calcification of coronary artery calcium without factoring in the calcium density as measured by the CAC Agatston Score. The CAC Score was log-transformed and the primary outcome measure was the change in Log CAC Volume Score from Baseline to Week 52 for the combined dose groups vs placebo. The primary analysis used an ANCOVA model with the change in log volume score (log 52-week volume score - log baseline volume

Interventions

  • DRUG Placebo
  • DRUG SNF472

Trial Details

FieldValue
Enrollment Target 274 participants
Start Date 2016-11
Est. Completion 2019-09
Phase Phase 2
Sanifit Therapeutics S. A.

4 total trials

What the finished NCT02966028 record still lists

NCT02966028 is an interventional study that assigns participants to a tested intervention. The registered 274 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (106% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02966028 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02966028 about?

NCT02966028 is a clinical study titled "Effect of SNF472 on Progression of Cardiovascular Calcification in End-Stage-Renal-Disease (ESRD) Patients on Hemodialysis (HD)". The primary objective is to assess the effect of 2 dose levels of SNF472 (300 mg and 600 mg) compared to placebo on the progression of coronary artery calcium volume score over a 12-month (52 weeks) period in ESRD patients on HD

What is the current status of trial NCT02966028?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 274 participants. The study started on 2016-11. Estimated completion is 2019-09.

What interventions are being tested in trial NCT02966028?

The interventions under investigation include: Placebo (DRUG), SNF472 (DRUG).

Who is sponsoring clinical trial NCT02966028?

This trial is sponsored by Sanifit Therapeutics S. A., which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02966028's enrollment target sits among peer trials

274 203rd of 2000 higher than 1,797 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02966028, the US trial registry maintained by the National Library of Medicine. NCT02966028 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.