Drugs / L-methylfolate

Trials 3 · a red edge is where a trial was stopped

2015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2/31 trial
Phase 2/3 NCT01853280 May 2014 → Feb 2017 attention deficit-hyperactivity disorder Massachusetts General Hospital Completed No outcome recorded
Phase 42 trials
Phase 4 NCT06218030 Oct 2024 → Apr 2026 overdue generalized anxiety disorder Queen's University Recruiting No outcome recorded
Phase 4 NCT04782037 Oct 2020 → Jul 2022 acute diarrhea King Edward Medical University Unknown No outcome recorded
Also used as a comparator or background therapy in 2 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 41 trial
Phase 4 NCT05807711 Comparator Apr 2023 → May 2024 end stage renal failure, renal hypertension Alexandria University Completed No outcome recorded
Phase not applicable1 trial
NCT02223299 Background Nov 2015 major depressive disorder John D. Dingell VA Medical Center Withdrawn No outcome recorded

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as L-methylfolate “Patients will be assigned to take one tablet daily containing L-methylfolate and methylcobalamine.” NCT05807711
3

NCT04782037

NCT01853280

NCT06218030

Known as deplin ClinicalTrials.gov intervention name — accepted as the source's own label NCT02223299
Route Oral Oral administration of L-methylfolate 15 mg per day for 8 weeks.” NCT06218030