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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of BCX7353 as an Oral Treatment for the Prevention of Attacks in HAE

ClinicalTrials.gov ID: NCT03485911

Public ClinicalTrials.gov record NCT03485911. 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 Jul 22, 2026, 1:57 AM EDT

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

Official title

A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Two Dose Levels of BCX7353 as an Oral Treatment for the Prevention of Attacks in Subjects With Hereditary Angioedema

Study identification

NCT ID
NCT03485911
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
BioCryst Pharmaceuticals
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

  • BCX7353 capsules Drug
  • Placebo oral capsule Drug

Drug

Eligibility (public fields only)

Age range
12 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
Feb 5, 2018
Primary completion
Apr 9, 2019
Completion
Apr 5, 2022
Last update posted
Jun 25, 2023

2018 – 2022

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
27
Facility City State ZIP Site status
Study center Birmingham Alabama 35209
Study center Scottsdale Arizona 85251
Study center Little Rock Arkansas 72205
Study Center San Diego California 92122
Study center Santa Monica California 90404
Study Center Walnut Creek California 94598
Study center Colorado Springs Colorado 80907
Study Center Tampa Florida 33613
Study center Chevy Chase Maryland 20815
Study Center Boston Massachusetts 02114
Study Center Ann Arbor Michigan 48106
Study center Plymouth Minnesota 55446
Study Center St Louis Missouri 63141
Study center Belleville New Jersey 07109
Study Center Fair Lawn New Jersey 07410
Study center Piscataway New Jersey 08854
Study Center New York New York 10029
Study Site Charlotte North Carolina 28277
Study Center Durham North Carolina 27705
Study Center Cincinnati Ohio 45231
Study center Columbus Ohio 43235
Study center Clackamas Oregon 97015
Study Center Hershey Pennsylvania 17033
Study center Austin Texas 78731
Study center Dallas Texas 75231
Study Center San Antonio Texas 78229
Study Center Spokane Washington 99202

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03485911, 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 Jun 25, 2023 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03485911 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →