ICD M35.2ORPHA:117BD

Behcet's Disease

Behcet's disease is a rare systemic vasculitis causing recurrent oral ulcers, genital ulcers, eye inflammation, and skin lesions. It is more prevalent in people from the Middle East, Turkey, and East Asia. Treatment depends on which organs are affected, with immunosuppressants and newer biologics increasingly used.

276
Articles
67
Trials (2 AU)
Updated
26 March 2026
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Common Questions

What is Behcet's Disease?

Behcet's disease is a rare systemic vasculitis causing recurrent oral ulcers, genital ulcers, eye inflammation, and skin lesions. It is more prevalent in people from the Middle East, Turkey, and East Asia. Treatment depends on which organs are affected, with immunosuppressants and newer biologics increasingly used.

How many clinical trials are available for Behcet's Disease?

RareWays currently indexes 67 clinical trials for Behcet's Disease, of which 16 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Behcet's Disease come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.