RT001 clinical trials
Also written RT001.
How each study uses RT001 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
How studies write it
Studies that test it under each name
Studies by the year they started
9 studies that test it; most in 2009 (2)
| Year | Studies |
|---|---|
| 2008 | 1 |
| 2009 | 2 |
| 2010 | 2 |
| 2018 | 1 |
| 2019 | 1 |
| 2021 | 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 9 · Other 0
Revance Therapeutics, Inc. (5) · Retrotope, Inc. (3) · Biojiva LLC (1)
Studies
Open first, then newest update. How each study uses RT001 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 · 9
- RT001 in Amyotrophic Lateral SclerosisCompletedPhase 2Biojiva LLCNCT04762589Written as RT001
- A Study to Assess Efficacy, Long Term Safety and Tolerability of RT001 in Subjects With Friedreich's AtaxiaCompletedPhase 3Retrotope, Inc.NCT04102501Written as RT001
- A Study to Assess Efficacy and Safety of RT001 in Subjects With Infantile Neuroaxonal DystrophyActive, not recruitingPhase 2/3Retrotope, Inc.NCT03570931Written as RT001
- RT001 in Patients With Progressive Supranuclear Palsy (PSP) PROGRESSIVE SUPRANUCLEAR PALSYStatus unknownPhase 2Retrotope, Inc.NCT04937530Written as RT001
- Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal LinesCompletedPhase 2Revance Therapeutics, Inc.NCT00884234Written as RT001 (Botulinum Toxin Type A Topical Gel)
- A 4-Arm Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in AdultsCompletedPhase 2Revance Therapeutics, Inc.NCT01124552Written as RT001 Botulinum toxin type A (Dose A)
- Safety Study of Two Repeat Doses of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in AdultsCompletedPhase 2Revance Therapeutics, Inc.NCT01124565Written as RT001
- Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal LinesCompletedPhase 2Revance Therapeutics, Inc.NCT00907387Written as RT001
- Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal LinesCompletedPhase 2Revance Therapeutics, Inc.NCT00888914Written as RT001