New drug HRS-3095 aims to soothe stubborn hives

NCT ID NCT07613866

First seen Jun 25, 2026 · Last updated Jun 25, 2026

Summary

This Phase 2 trial tests whether the experimental drug HRS-3095 can reduce itching and wheals in adults with chronic spontaneous urticaria (hives) that isn't well controlled by antihistamines. About 190 participants will receive either the drug or a placebo daily for 4 weeks. The main goal is to see if the drug improves hive activity scores compared to placebo.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University

    Hangzhou, Zhejiang, 310006, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

  • Huashan Hospital Affiliated to Fudan University

    Shanghai, Shanghai Municipality, 200040, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

HRS-3095 tablet

What this could lead to

If it works, this could point toward a new daily pill to better control chronic hives for people who don't get enough relief from antihistamines.

What could go wrong

This is an early Phase 2 trial with only 190 participants, so results may not apply to everyone. The drug may not prove more effective than placebo, and side effects are still being studied.

Conditions

The condition(s) this trial relates to.

chronic idiopathic urticaria Chronic Urticaria

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.