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NCT05526391 · ClinicalTrials.gov registry record · Phase 2

A Study of TAK-341 in Treatment of Multiple System Atrophy

A Phase 2 study, sponsored by Takeda.

Completed
Registry status
Phase 2
Development phase
158
Enrollment target

NCT05526391: Completed Phase 2 study, sponsored by Takeda.

NCT05526391 is a Phase 2 study that has completed, run by Takeda. The registered enrollment target is 158 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05526391, a Phase 2 study, has completed, sponsored by Takeda.

COMPLETED
Registry status
Phase 2
Development phase
158 participants
Enrollment target

Study Summary

The main aim is to see how TAK-341 works after 52 weeks in participants with multiple system atrophy as measured by the Unified Multiple System Atrophy Rating Scale Part I (UMSARS). The study will enroll approximately 138 patients. Participants will receive a total of 13 intravenous infusions every 4 weeks approximately, these may be either of TAK-341 or placebo, after each infusion some blood samplings will be taken and other assessments completed. This trial will be conducted in North America, Europe and Asia.

Primary Outcome

UMSARS Part I (historical review) is a 12-item scale that was adapted from the Unified Parkinson's Disease Rating Scale (UPDRS) and is used to assess activities related to motor disability and autonomic dysfunction. In this study, the UMSARS was modified to exclude the sexual function item. Thus, total 11 items were assessed. Each item was initially scored on a scale from 0 (normal) to 4 (severe); ratings of normal (0) and mild (1) were then combined and recorded as 0, making minimum score 0 and

Interventions

  • DRUG Placebo
  • DRUG TAK-341

Trial Details

FieldValue
Enrollment Target 158 participants
Start Date 2022-11-16
Est. Completion 2025-07-28
Phase Phase 2
Takeda

408 total trials

What the finished NCT05526391 record still lists

NCT05526391 is an interventional study that assigns participants to a tested intervention. The registered 158 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05526391 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05526391 about?

NCT05526391 is a clinical study titled "A Study of TAK-341 in Treatment of Multiple System Atrophy". The main aim is to see how TAK-341 works after 52 weeks in participants with multiple system atrophy as measured by the Unified Multiple System Atrophy Rating Scale Part I (UMSARS). The study will enroll approximately 138 patients. Participants will receive a total of 13 intravenous infusions every...

What is the current status of trial NCT05526391?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 158 participants. The study started on 2022-11-16. Estimated completion is 2025-07-28.

What interventions are being tested in trial NCT05526391?

The interventions under investigation include: Placebo (DRUG), TAK-341 (DRUG).

Who is sponsoring clinical trial NCT05526391?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05526391's enrollment target sits among peer trials

158 443rd of 2000 higher than 1,558 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05526391, the US trial registry maintained by the National Library of Medicine. NCT05526391 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.