Indication

Familial cold autoinflammatory syndrome

Familial cold autoinflammatory syndrome (FCAS), formerly known as familial cold urticaria, is a rare, lifelong hereditary systemic autoinflammatory disorder that represents the mildest phenotype within the spectrum of cryopyrin-associated periodic syndromes (CAPS). Read more about Familial cold autoinflammatory syndrome

5 drugs 4 manufacturers

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Drugs that treat it

Common Familial cold autoinflammatory syndrome therapies.

Showing 1–5 of 5 drugs

ILARIS (canakinumab/PF)

ANTI-INFLAMMATORY - INTERLEUKIN 1 RECEPTOR ANTAGONIST·ACUTE GOUTY ARTHRITIS·+7
Novartis Pharmaceuticals

ARCALYST (rilonacept)

ANTI-INFLAMMATORY - INTERLEUKIN 1 RECEPTOR ANTAGONIST·MUCKLE-WELLS SYNDROME·+3
KINIKSA PHARMAC

ILARIS (canakinumab/PF)

ANTI-INFLAMMATORY - INTERLEUKIN 1 RECEPTOR ANTAGONIST·ACUTE GOUTY ARTHRITIS·+7
Novartis Pharmaceuticals
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About Familial cold autoinflammatory syndrome.

Familial cold autoinflammatory syndrome (FCAS), formerly known as familial cold urticaria, is a rare, lifelong hereditary systemic autoinflammatory disorder that represents the mildest phenotype within the spectrum of cryopyrin-associated periodic syndromes (CAPS).

Typically inherited in an autosomal dominant manner and manifesting in early infancy, the condition predominantly arises from gain-of-function variants in the *NLRP3* gene, driving hyperactivation of the cryopyrin inflammasome and aberrant, excessive release of interleukin-1 beta.

Clinically, FCAS is defined by recurrent, self-limited inflammatory episodes provoked within hours of generalized exposure to ambient cold or rapid temperature drops.

Hallmark manifestations of these flares, which usually resolve within 24 hours, include an itchy or burning urticaria-like rash, low-grade fevers, arthralgias, conjunctival injection, profound fatigue, and constitutional symptoms.

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