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Completed Phase 3 Interventional

Study of Efficacy, Safety of Fulranumab Monotherapy for OA of Hip or Knee, PAI3002

ClinicalTrials.gov ID: NCT02336698

Public ClinicalTrials.gov record NCT02336698. 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 22, 2026, 8:18 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

Randomized, 16-Week, Multi-Phase, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fulranumab as Monotherapy in Subjects With Signs and Symptoms of Osteoarthritis of the Hip or Knee

Brief summary

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

The purpose of this study is to demonstrate the efficacy, safety, and tolerability of fulranumab as Monotherapy compared with placebo in participants with signs and symptoms of osteoarthritis of the hip or knee that are not adequately controlled by current pain therapy.

Study identification

NCT ID
NCT02336698
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
18 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Jul 13, 2015 (Actual)
Primary completion
Sep 15, 2016 (Actual)
Completion
Sep 15, 2016 (Actual)
Last update posted
Oct 2, 2017

2015 – 2016

United States locations

U.S. sites
26
U.S. states
14
U.S. cities
26
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Costa Mesa California — —
Not listed Laguna Hills California — —
Not listed Lakewood California — —
Not listed Northridge California — —
Not listed Santa Clarita California — —
Not listed Thousand Oaks California — —
Not listed Boynton Beach Florida — —
Not listed Lake Clarke Shores Florida — —
Not listed Miami Florida — —
Not listed Atlanta Georgia — —
Not listed Chicago Illinois — —
Not listed Wichita Kansas — —
Not listed Bay City Michigan — —
Not listed Caro Michigan — —
Not listed Grand Rapids Michigan — —
Not listed Somerset New Jersey — —
Not listed Greenville North Carolina — —
Not listed Charleston South Carolina — —
Not listed Memphis Tennessee — —
Not listed Bedford Texas — —
Not listed Cypress Texas — —
Not listed Houston Texas — —
Not listed Waxahachie Texas — —
Not listed Riverton Utah — —
Not listed Norfolk Virginia — —

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 NCT02336698, 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 2, 2017 · Synced Oct 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 public registry record, listed eligibility criteria, and available contact information for NCT02336698 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →