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NCT04642742
Impact of a Chewable Plant Sterol Supplement on LDL-C in A Real-World Setting
trial testing Chewable plant sterol in Hyperlipidemia in 150 participants. Status unknown.
11 November 2021
Quick facts
| Lead sponsor | Piper Biosciences, Inc. |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 150 |
| Start date | 25 November 2020 |
| Primary completion | 11 November 2021 |
| Estimated completion | 11 November 2021 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Chewable plant sterol
Conditions studied
- Hyperlipidemia — all drugs for Hyperlipidemia →
Sponsor
Piper Biosciences, Inc.
Who can join
18 and older, any sex, with Hyperlipidemia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to measure the effectiveness of a twice daily plant sterol supplement, which is in a gummy format and packaged with health insights, in reducing LDL-C cholesterol in a real word setting.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04642742
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT04642742 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Piper Biosciences, Inc.
- Last refreshed: 24 November 2020
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/NCT04642742.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing