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ACTIVE NOT RECRUITING Phase 2

A Phase 2 in Adult Subjects With Hereditary Angioedema

NCT06846398 · View on ClinicalTrials.gov ↗

Study Summary

A Phase 2 in Adult Subjects with Hereditary Angioedema

Interventions

  • DRUG BW-20805

Study Locations (18)

Maryland

  • Institute for Asthma and Allergy - Wheaton — Silver Spring

Missouri

  • Washington University School of Medicine — St Louis

North Carolina

  • Duke University Medicine Center — Durham

Pennsylvania

  • Penn State Milton S. Hershey MC - Penn State — Hershey

Virginia

  • Inova Clinical Trials and Research Center — Falls Church

Beijing Municipality

  • Peking Union Medical College Hospital — Beijing

Gansu

  • The First Hospital of Lanzhou University — Lanzhou

Hubei

  • Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology — Wuhan

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2025-02-28
Est. Completion 2028-03-30
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06846398

The ClinicalTrials.gov registry entry for NCT06846398 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Shanghai Argo Biopharmaceutical Co., which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hereditary Angioedema (HAE) appearing as the primary indexed condition, and to 1 intervention — of which BW-20805 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06846398 reports 18 study locations spanning 18 distinct geographic areas — top geographies include Maryland, Missouri, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06846398 about?

NCT06846398 is a clinical study titled "A Phase 2 in Adult Subjects With Hereditary Angioedema". A Phase 2 in Adult Subjects with Hereditary Angioedema

What is the current status of trial NCT06846398?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2025-02-28. Estimated completion is 2028-03-30.

What conditions does trial NCT06846398 study?

This clinical trial studies the following conditions: Hereditary Angioedema (HAE). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06846398?

The interventions under investigation include: BW-20805 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06846398?

This trial is sponsored by Shanghai Argo Biopharmaceutical Co., which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06846398 being conducted?

This trial has 18 study locations across Maryland, Missouri, North Carolina, Pennsylvania, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial