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Completed Phase 2Phase 3 Interventional Results available

12-Week Safety and Efficacy Study of BCX4161 as an Oral Prophylaxis Against HAE Attacks

ClinicalTrials.gov ID: NCT02303626

Public ClinicalTrials.gov record NCT02303626. 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, 11:46 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

OPuS-2: A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Two Dose Levels of BCX4161 for 12 Weeks as an Oral Prophylaxis Treatment for Attacks of Hereditary Angioedema

Study identification

NCT ID
NCT02303626
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
BioCryst Pharmaceuticals
Industry
Enrollment
110 participants

Conditions and interventions

Interventions

  • BCX4161 Drug
  • Placebo Drug

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
Dec 16, 2014
Primary completion
Dec 31, 2015
Completion
Dec 31, 2015
Last update posted
Nov 16, 2025

2014 – 2016

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Not listed Birmingham Alabama 35209
Not listed Scottsdale Arizona 85251
Not listed Granada Hills California 91344
Not listed San Diego California 92093
Not listed San Diego California 92112
Not listed Walnut Creek California 94598
Not listed Colorado Springs Colorado 80907
Not listed Shreveport Louisiana 71106
Not listed Chevy Chase Maryland 20815
Not listed Boston Massachusetts 02114
Not listed Plymouth Minnesota 55446
Not listed St Louis Missouri 63141
Not listed New York New York 10029
Not listed Charlotte North Carolina 28277
Not listed Cincinnati Ohio 45267
Not listed Oklahoma City Oklahoma 73131
Not listed Tulsa Oklahoma 74133
Not listed Lake Oswego Oregon 97035
Not listed Hershey Pennsylvania 17033
Not listed Pittsburgh Pennsylvania 15241
Not listed Dallas Texas 75231
Not listed Galveston Texas 77555
Not listed Fairfax Virginia 63141
Not listed Spokane Washington 99204
Not listed Tacoma Washington 98405

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02303626, 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 Nov 16, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02303626 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →