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AvailableNCT07531433Updated Apr 15, 2026

Post-Trial Access to ATH434 for Patients With Multiple System Atrophy

An expanded access record providing ATH434 in Multiple System Atrophy, sponsored by Alterity Therapeutics. Available. Per ClinicalTrials.gov, last updated 2026-04-15.

Sponsored by Alterity Therapeutics · Expanded access

Study type
Expanded access
Access type
Intermediate-size population
Sex
All
01

Study summary

This multicenter post-trial access program is designed to provide ATH434 orally BID to eligible patients who completed Phase 2 studies ATH434-201 or ATH434-202, and who may benefit from this treatment according to the evaluation by their treating physicians.

Read the detailed description

This multicenter PTA program is designed to provide ATH434 orally BID to eligible patients who have completed the ATH434-201 or ATH434-202 Phase 2 clinical trials, and who may benefit from this treatment according to evaluation by their treating physician. Up to 20 patients will be enrolled in the US.

For each patient, treating physicians will request participation in the PTA study and initial ATH434 shipment for patients who meet entry criteria. Upon review and approval by the Medical Monitor/Sponsor, treating physicians will obtain informed consent from the patient and proceed with ATH434 initiation under the PTA program. Pertinent documented medical information will be requested to confirm eligibility and assess patient safety throughout the PTA program.

Eligible patients will receive ATH434 tablets BID to be taken with food for up to 12 months, and will complete in-clinic and remote visits for safety and to dispense/return ATH434.

02

Conditions studied

  • Multiple System Atrophy
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All

Inclusion criteria

  • Completed Alterity protocol ATH434-201 or ATH434-202
  • Expected to benefit from treatment from treatment with ATH434, in the opinion of the treating physician

Exclusion criteria

Exclusion Criteria:

  • Discontinued prior ATH434 treatment (ATH434-201 or ATH434-202) for any reason
  • Significant medical or psychiatric condition that may decrease the benefit-risk ratio of participation in this program to an unacceptable level, as per the treating physician's opinion
04

Access details

Study type
Expanded access
Access type
Intermediate-size population

Available treatment

  • DrugATH434

    ATH434 tablets

    Also known as: PBT434

05

Where to request access

No study locations are listed for this record.

06

Registry details

Key details

Study ID
NCT07531433
Lead sponsor
Alterity Therapeutics
Responsible party
Sponsor
First posted
Apr 15, 2026
Last update
Apr 15, 2026

Study contacts

Alterity Clinical Trials
Contact
clinicaltrials@alteritytx.com
888-556-7582
View the source record on ClinicalTrials.gov ↗

Requesting access

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