EligibleTrials

Anifrolumab: clinical trials recruiting now

8
Recruiting trials
5
Conditions studied
24
US states with sites
20
Countries

FDA drug label

FDA-approved
Yes. Anifrolumab appears in the FDA drug-label database. Marketed as SAPHNELO.
Drug class
Type I Interferon Receptor Antagonist (FDA established pharmacologic class)
Mechanism of action
Type I Interferon Receptor Antagonists (as stated on the FDA label)

FDA-approved use

SAPHNELO is indicated for the treatment of adult patients with moderate to severe systemic lupus erythematosus (SLE), who are receiving standard therapy. Limitations of Use The efficacy of SAPHNELO has not been evaluated in patients with severe active lupus nephritis or severe active central nervous system lupus. Use of SAPHNELO is not recommended in these situations. SAPHNELO is a type I interferon (IFN) receptor antagonist indicated for the treatment of adult patients with moderate to severe systemic lupus erythematosus (SLE), who are receiving standard therapy. ( 1 ) Limitations of Use: The efficacy of SAPHNELO has not been evaluated in patients with severe active lupus nephritis or severe active central nervous system lupus. Use of SAPHNELO is not recommended in these situations. ( 1 )

FDA label via openFDA

Phase breakdown

Phase 2 1 Phase 3 2 Phase 4 1 Not applicable 4

Conditions being studied

ConditionTrials
Lupus · Anifrolumab for Lupus8
Systemic Lupus Erythematosus · Anifrolumab for Systemic Lupus Erythematosus7
Cardiovascular Disease1
Lupus Erythematosus, Systemic1
Premature Atherosclerosis1

Recruiting trials involving Anifrolumab

Common questions

Is Anifrolumab FDA-approved?

Yes, marketed as SAPHNELO.

How many recruiting trials involve Anifrolumab?

8 recruiting trials across 5 conditions.

Is this list of trials complete?

No. For the full record, search ClinicalTrials.gov.

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