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NCT02683239 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by Regeneron Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
5,331
Enrollment target

NCT02683239: Completed Phase 3 study, sponsored by Regeneron Pharmaceuticals.

NCT02683239 is a Phase 3 study that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 5,331 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (591% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02683239, a Phase 3 study, has completed, sponsored by Regeneron Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
5,331 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Placebo
  • DRUG Fasinumab

Trial Details

FieldValue
Enrollment Target 5,331 participants
Start Date 2016-02-17
Est. Completion 2021-06-15
Phase Phase 3
Regeneron Pharmaceuticals

280 total trials

What the finished NCT02683239 record still lists

NCT02683239 is an interventional study that assigns participants to a tested intervention. Its 5,331 participants enrollment target places it among the larger protocols in the corpus, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (591% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02683239 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02683239 about?

NCT02683239 is a clinical study titled "Long-Term Safety and Efficacy Study of Fasinumab in Patients With Pain Due to Osteoarthritis (OA) of the Knee or Hip". 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.

What is the current status of trial NCT02683239?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 5,331 participants. The study started on 2016-02-17. Estimated completion is 2021-06-15.

What interventions are being tested in trial NCT02683239?

The interventions under investigation include: Placebo (DRUG), Fasinumab (DRUG).

Who is sponsoring clinical trial NCT02683239?

This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02683239's enrollment target sits among peer trials

5,331 46th of 2000 higher than 1,955 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02683239, the US trial registry maintained by the National Library of Medicine. NCT02683239 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.