R-1,3-Butanediol-based Supplement clinical trials
- studies test it
- 3
- open now
- 0
- in phase 3
- 0
- first study started
- 2024
How each study uses R-1,3-Butanediol-based Supplement is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
Studies by the year they started
3 studies that test it; most in 2025 (2)
| Year | Studies |
|---|---|
| 2024 | 1 |
| 2025 | 2 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 0 · Other 3
Johns Hopkins University (2) · Gødstrup Hospital (1)
Studies
Open first, then newest update. How each study uses R-1,3-Butanediol-based Supplement is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 3
- Impact of Exogenous Ketones on Sleep ApneaWithdrawnPhase 1/2Johns Hopkins UniversityNCT06687655Written as Ketone-IQ
- Effects of Exogenous Ketosis on Proteinuria and Renal FunctionCompletedNot applicableGødstrup HospitalNCT06867471Written as Ketone Diol, R-1,3-butanediol (Ketone-IQ)
- Impact of Exogenous Ketones on Sleep Disruption in Vulnerable PopulationsSuspendedPhase 1Johns Hopkins UniversityNCT06655649Written as Ketone-IQ (1,3 Butanediol)