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Completed No phase listed Observational

Study Evaluating "Real World" Treatment Pattern in Previously Treated Hemophilia A Patients Receiving KOVALTRY (Octocog Alfa) for Routine Prophylaxis

ClinicalTrials.gov ID: NCT02830477

Public ClinicalTrials.gov record NCT02830477. 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 Sep 2, 2026, 3:02 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 Multinational Phase IV Study Evaluating "Real World" Treatment Pattern in Previously Treated Hemophilia A Patients Receiving KOVALTRY (Octocog Alfa) for Routine Prophylaxis

Brief summary

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

The primary objective of this study is to investigate weekly prophylaxis dosing regimens used in standard clinical practice. In addition the study will capture reported bleed rate, pattern of change in KOVALTRY prophylaxis dose \& dosing frequency, reason for choice of treatment regimen, FVIII product switch pattern, patient treatment satisfaction and adherence, KOVALTRY pharmacokinetic data (if performed), KOVALTRY consumption, as well as safety data.

Study identification

NCT ID
NCT02830477
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
313 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
Male
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
Oct 13, 2016
Primary completion
Nov 30, 2020
Completion
Feb 28, 2021
Last update posted
Nov 6, 2023

2016 – 2021

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Children's Rehabilitation Services/ University of South Alabama Mobile Alabama
University of Colorado Hemophilia and Thrombosis Center Aurora Colorado
University of Florida Health Cancer Center Gainesville Florida
Nemours Children's Clinic - Division of Pediatric Hematology/Oncology - Jacksonsville Jacksonville Florida
Nemours Children's Clinic - Pensacola Pensacola Florida
Henry Ford Hospital Adult Hemophilia and Thrombosis Treatment Center Detroit Michigan
Washington University Center for Bleeding and Blood Clotting Disorders St Louis Missouri
Hemophilia Center of Western New York Buffalo New York
East Carolina University - Brody School of Medicine Greenville North Carolina
Wake Forest University School of Medicine Winston-Salem North Carolina
Children's Hospital at OU Medical Center Oklahoma City Oklahoma
Intermountain Hemophilia & Thrombosis Center Salt Lake City Utah
Comprehensive Center for Bleeding Disorders / Blood Center of Wisconsin Milwaukee Wisconsin

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02830477, 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 6, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02830477 live on ClinicalTrials.gov.

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