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A Study of Lu AF82422 in Participants With Multiple System Atrophy

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NCT05104476 · results posted

Sponsored by H. Lundbeck A/S (industry) · HLUN-B.CO — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
64actual
Sites
19
Countries
Japan, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-11-16actualWhen the study began enrolling
Primary completion2023-11-16actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-03-07estimatedThe whole study's end, after follow-up
First posted2021-11-03actualWhen this record first appeared on the registry
Results posted2024-12-27actualWhen the sponsor posted results to the registry
Record updated2026-04-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Multiple System Atrophy

Interventions

  • Drug: Lu AF82422
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Percentage Slowing of Clinical Progression Based on Change From Baseline in the UMSARS TS at the End of Treatment (EOT) DB Period (DBP)
measured Baseline up to Week 72

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2024-05-29 · 4.1 MB · Prot_000.pdf
Statistical Analysis Planposted 2023-12-20 · 2.5 MB · SAP_001.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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