NCT06927999Phase 2Recruiting

An Outpatient Study of the Efficacy of ARS-2 in Patients With Chronic Spontaneous Urticaria

Study sponsor: ARS Pharmaceuticals, Inc. · SPRY

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

Primary completion2027-06Estimated
Enrollment · participants42Estimated
Source updated2026-09-16Last update listed in the registry record
Version history

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· 1 field changed

Primary outcomes · main study measures

Text edit · unverified significance
− Previous value

measure: Determine the effect of ARS-2 (0.5 mg or 1 mg) versus placebo on itch and hive

+ Updated value

measure: Determine the effect of ARS-2 (0.5 mg or 1 mg) versus placebo on itch

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· 1 field changed

Primary completion date

Recorded edit
− Previous value

2026-06

+ Updated value

2027-06

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· 1 field changed

Recruitment status

Recorded edit
− Previous value

Not yet recruiting

+ Updated value

Recruiting

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