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Biomarker Study of ATH434 in Participants With MSA

A

Alterity Therapeutics

Status and phase

Not yet enrolling
Phase 2

Conditions

Multiple System Atrophy

Study type

Interventional

Funder types

Industry

Identifiers

NCT05732415
ATH434-202

Details and patient eligibility

About

This study will assess the safety and efficacy of ATH434 in participants with a clinical diagnosis of Multiple System Atrophy

Enrollment

15 estimated patients

Sex

All

Ages

30 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Participant has clinical features of parkinsonism. Participant has evidence of orthostatic hypotension and/or bladder dysfunction. Participant has ataxia and/or pyramidal signs on neurological examination. Participant has biomarker evidence of MSA in biologic fluid and on MRI.

Exclusion criteria

Participant is unable to swallow study drug. Participant is unable to attend study visits or complete study procedures. Participant has structural brain abnormality on MRI. Participant has any significant neurological disorder other than MSA. Participant has an unstable medical or psychiatric illness. Participant has a contraindication to, or is unable to tolerate, MRI or lumbar puncture.

Trial design

15 participants in 1 patient group

ATH434
Experimental group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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