Disease Directory Primary progressive apraxia of speech
Rare Disease

Primary progressive apraxia of speech

Type

Disease

About Primary progressive apraxia of speech

Primary progressive apraxia of speech is a rare disease catalogued by Orphanet (ORPHA:314566). Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries worldwide.

Clinical Trial Eligibility Tips

What to know before applying to Primary progressive apraxia of speech trials.

Search ClinicalTrials.gov for "Primary progressive apraxia of speech" or Orphanet code ORPHA:314566 to find disease-specific recruiting studies.

Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.

Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:314566)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Primary progressive apraxia of speech trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary progressive apraxia of speech. Updated daily.