deltatrials
Completed PHASE1 INTERVENTIONAL 2-arm NCT04493281

Bioequivalence Study of Oral Suspension and Intravenous Formulation of Edaravone in Healthy Adult Subjects

Sponsor: Tanabe Pharma Corporation

Interventions MCI-186 MT-1186
Updated 8 times since 2020 Last updated: Dec 15, 2025 Started: Mar 22, 2019 Primary completion: Apr 21, 2019 Completion: May 9, 2019
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE1 clinical study on Healthy Adult Subjects, this trial is completed. The trial is conducted by Tanabe Pharma Corporation and has accumulated 8 data snapshots since 2019. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Aug 2020 – ~Sep 2020 · 31 days · monthly snapshotCompleted~Sep 2020 – ~Jan 2021 · 4 months · monthly snapshotCompleted~Jan 2021 – ~Feb 2024 · 37 months · monthly snapshotCompleted~Feb 2024 – ~Jul 2024 · 5 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Jan 2026 · 16 months · monthly snapshotCompleted~Jan 2026 – ~Feb 2026 · 31 days · monthly snapshotCompleted~Feb 2026 – present · 5 months · monthly snapshotCompleted

Change History

8 versions recorded
  1. Feb 2026 — Present [monthly]

    Completed PHASE1

  2. Jan 2026 — Feb 2026 [monthly]

    Completed PHASE1

  3. Sep 2024 — Jan 2026 [monthly]

    Completed PHASE1

  4. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE1

  5. Feb 2024 — Jul 2024 [monthly]

    Completed PHASE1

Show 3 earlier versions
  1. Jan 2021 — Feb 2024 [monthly]

    Completed PHASE1

  2. Sep 2020 — Jan 2021 [monthly]

    Completed PHASE1

  3. Aug 2020 — Sep 2020 [monthly]

    Completed PHASE1

    First recorded

Mar 2019

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Tanabe Pharma Corporation
Data source: Tanabe Pharma Corporation

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations