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Completed Phase 3 Interventional Results available

Long-Term Safety and Efficacy Study of Fasinumab in Patients With Pain Due to Osteoarthritis (OA) of the Knee or Hip

ClinicalTrials.gov ID: NCT02683239

Public ClinicalTrials.gov record NCT02683239. 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 Oct 5, 2026, 10:29 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, Multi-Dose, Placebo-Controlled Study to Evaluate the Long-Term Safety and the Efficacy of Fasinumab in Patients With Pain Due to Osteoarthritis of the Knee or Hip

Brief summary

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

The primary objective of the study is to describe the safety and tolerability of fasinumab, including adverse events of special interest (AESIs), in patients with pain due to radiographically-confirmed OA of the knee or hip.

Study identification

NCT ID
NCT02683239
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
5,331 participants

Conditions and interventions

Interventions

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
Feb 17, 2016 (Actual)
Primary completion
Dec 1, 2020 (Actual)
Completion
Jun 15, 2021 (Actual)
Last update posted
Oct 13, 2023

2016 – 2021

United States locations

U.S. sites
50
U.S. states
22
U.S. cities
47
Facility City State ZIP Site status
Regeneron Investigational Site Birmingham Alabama 35211 —
Regeneron Investigational Site #1 Chandler Arizona 85224 —
Regeneron Investigational Site #2 Chandler Arizona 85224 —
Regeneron Investigational Site Glendale Arizona 85308 —
Regeneron Investigational Site Mesa Arizona 85213 —
Regeneron Investigational Site (4 locations) Phoenix Arizona 85018 —
Regeneron Investigational Site Tempe Arizona 85224 —
Regeneron Investigational Site (2 locations) Tucson Arizona 85712 —
Regeneron Investigational Site Little Rock Arkansas 72205 —
Regeneron Investigational Site Beverly Hills California 90211 —
Regeneron Investigational Site Carlsbad California 92008 —
Regeneron Investigational Site San Diego California 92103 —
Regeneron Investigational Site San Marcos California 92078 —
Regeneron Investigational Site Vista California 92083 —
Regeneron Investigational Site Aurora Colorado 80014 —
Regeneron Investigational Site Colorado Springs Colorado 80909 —
Regeneron Investigational Site Golden Colorado 80401 —
Regeneron Investigational Site Littleton Colorado 80127 —
Regeneron Investigational Site Clearwater Florida 33765 —
Regeneron Investigational Site Orlando Florida 32801 —
Regeneron Investigational Site Pinellas Park Florida 33781 —
Regeneron Investigational Site Atlanta Georgia 30328 —
Regeneron Investigational Site (3 locations) Chicago Illinois 60602 —
Regeneron Investigational Site Evansville Illinois 47714 —
Regeneron Investigational Site Kansas City Kansas 64114 —
Regeneron Investigational Site Frederick Maryland 21702 —
Regeneron Investigational Site Worcester Massachusetts 01605 —
Regeneron Investigational Site Richfield Minnesota 55423 —
Regeneron Investigational Site #1 St Louis Missouri 63141 —
Regeneron Investigational Site #2 St Louis Missouri 63141 —
Regeneron Investigational Site Elkhorn Nebraska 68022 —
Regeneron Investigational Site Fremont Nebraska 68025 —
Regeneron Investigational Site Omaha Nebraska 68144 —
Regeneron Investigational Site Las Vegas Nevada 89128 —
Regeneron Investigational Site Jamaica New York 11432 —
Regeneron Investigational Site New York New York 10036 —
Regeneron Investigational Site High Point North Carolina 27262 —
Regeneron Investigational Site Akron Ohio 44311 —
Regeneron Investigational Site Cincinnati Ohio 45219 —
Regeneron Investigational Site Columbus Ohio 43212 —
Regeneron Investigational Site Oklahoma City Oklahoma 73119 —
Regeneron Investigational Site Duncansville Pennsylvania 16635 —
Regeneron Investigational Site Anderson South Carolina 29621 —
Regeneron Investigational Site Greer South Carolina 29651 —
Regeneron Investigational Site #1 Dallas Texas 75234 —
Regeneron Investigational Site #2 Dallas Texas 75234 —
Regeneron Investigational Site Houston Texas 77008 —
Regeneron Investigational Site Lubbock Texas 79424 —
Regeneron Investigational Site Plano Texas 75093 —
Regeneron Investigational Site San Antonio Texas 78229 —

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 99 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02683239, 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 Oct 13, 2023 · Synced Oct 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02683239 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →