ClinicalTrials.Veeva

Menu

A Biomarker Study of ATH434 in Participants With MSA

A

Alterity Therapeutics

Status and phase

Completed
Phase 2

Conditions

Multiple System Atrophy

Treatments

Drug: ATH434

Study type

Interventional

Funder types

Industry

Identifiers

NCT05864365
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

10 patients

Sex

All

Ages

30 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

ATH434
Experimental group
Treatment:
Drug: ATH434

Trial contacts and locations

1

Loading...

Central trial contact

Alterity Clinical Trials

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems