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Terminated Phase 2 Interventional

A Phase 2, Open-Label, Extension Study to Evaluate Long Term Safety and Clinical Activity of Briquilimab in Participants From Jasper-Sponsored Chronic Urticaria Trials

ClinicalTrials.gov ID: NCT06736262

Public ClinicalTrials.gov record NCT06736262. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 3, 2026, 8:08 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Open-Label Extension Study to Evaluate Long Term Safety and Clinical Activity of Briquilimab in Chronic Urticaria

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Phase 2, open-label, extension study to evaluate the long-term safety, clinical activity, and pharmacodynamics of briquilimab in participants previously enrolled in a Jasper sponsored CU clinical trial.

Study identification

NCT ID
NCT06736262
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Jasper Therapeutics, Inc.
Industry
Enrollment
67 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 26, 2024 (Actual)
Primary completion
Jul 21, 2026 (Actual)
Completion
Jul 21, 2026 (Actual)
Last update posted
Aug 6, 2026

2024 – 2026

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Investigative Site 118 Birmingham Alabama 35244 —
Investigative Site 108 Little Rock Arkansas 72205 —
Investigative Site 105 San Diego California 92123 —
Investigative Site 116 Tampa Florida 33613 —
Investigative Site 109 Boise Idaho 83706 —
Investigative Site 124 Normal Illinois 61761 —
Investigative Site 110 Indianapolis Indiana 46250 —
Investigative Site 123 Lafayette Louisiana 70508 —
Investigative Site 101 Baltimore Maryland 21224 —
Investigative Site 121 White Marsh Maryland 21162 —
Investigative Site 103 Cincinnati Ohio 45236 —
Investigative Site 111 Murray Utah 84107 —
Investigative Site 115 Seattle Washington 98101 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06736262, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 6, 2026 · Synced Oct 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06736262 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →