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Completed Phase 2 Interventional Results available

Subcutaneous CINRYZE With Recombinant Human Hyaluronidase for Prevention of Angioedema Attacks

ClinicalTrials.gov ID: NCT01756157

Public ClinicalTrials.gov record NCT01756157. 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, 12:39 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

A Phase 2, Randomized, Double-Blind, Multicenter, Dose-Ranging, Crossover Study to Evaluate the Safety and Efficacy of Subcutaneous Administration of CINRYZE® (C1 Esterase Inhibitor [Human]) With Recombinant Human Hyaluronidase (rHuPH20) for the Prevention of Angioedema Attacks in Adolescents and Adults With Hereditary Angioedema

Study identification

NCT ID
NCT01756157
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Shire
Industry
Enrollment
47 participants

Conditions and interventions

Interventions

  • CINRYZE with rHuPH20 Biological

Biological

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 3, 2013
Primary completion
Sep 12, 2013
Completion
Sep 12, 2013
Last update posted
Jun 2, 2021

2013

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
ViroPharma Investigational Site Birmingham Alabama 35209
ViroPharma Investigational Site Scottsdale Arizona 85251
ViroPharma Investigational Site Bentonville Arkansas 72712
ViroPharma Investigational Site Walnut Creek California 94598
ViroPharma Investigational Site Colorado Springs Colorado 80907
ViroPharma Investigational Site Tampa Florida 33613
ViroPharma Investigational Site Boston Massachusetts 02114
ViroPharma Investigational Site Las Vegas Nevada 89106
ViroPharma Investigational Site Mineola New York 11501
ViroPharma Investigational Site Cincinnati Ohio 45267
ViroPharma Investigational Site Columbus Ohio 43235
ViroPharma Investigational Site Lake Oswego Oregon 97035
ViroPharma Investigational Site Hershey Pennsylvania 17033
ViroPharma Investigational Site Pittsburgh Pennsylvania 15241
ViroPharma Investigational Site Knoxville Tennessee 37909
ViroPharma Investigational Site Dallas Texas 75231
ViroPharma Investigational Site Spokane Washington 99204

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 NCT01756157, 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 2, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01756157 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →