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NCT03691974 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Effects of Fasinumab on Peripheral Nerve Function in Patients With Pain Due to Osteoarthritis of the Hip or Knee

A Phase 2 study of Osteoarthritis, Knee and Osteoarthritis, Hip, sponsored by Regeneron Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
180
Enrollment target
20
Study locations

NCT03691974: Completed Phase 2 study of Osteoarthritis, Knee and Osteoarthritis, Hip, sponsored by Regeneron Pharmaceuticals.

NCT03691974 is a Phase 2 study of Osteoarthritis, Knee and Osteoarthritis, Hip that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 180 participants, below the 496-participant average among 112 other Osteoarthritis, Knee trials with a reported enrollment target (64% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03691974, a Phase 2 study of Osteoarthritis, Knee and Osteoarthritis, Hip, has completed, sponsored by Regeneron Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
180 participants
Enrollment target
20
Study locations

Study Summary

The primary objective of the study is to evaluate the effect of fasinumab compared to placebo on peripheral nerves in participants with pain due to Osteoarthritis (OA) of the hip or knee. The secondary objectives of the study are to: * Evaluate the efficacy of fasinumab compared to placebo in participants with pain due to OA of the hip or knee * Evaluate the safety and tolerability of fasinumab compared to placebo in participants with pain due to OA of the hip or knee * Characterize the concentrations of fasinumab in serum in participants with pain due to OA of the hip or knee * Evaluate the immunogenicity of fasinumab in participants with pain due to OA of the hip or knee.

Primary Outcome

Peroneal motor nerve conduction velocity was evaluated by electrical stimulation of the nerve and recorded the compound muscle action potential from surface electrodes overlying a muscle supplied by the nerve. Change from baseline in peroneal motor nerve conduction velocity at Week 16 was reported.

Interventions

  • OTHER Placebo
  • DRUG Fasinumab

Study Locations (20)

Florida

  • Regeneron Study Site - Clearwater
  • Regeneron Study Site - Jacksonville
  • Regeneron Study Site - Miami
  • Regeneron Study Site - Ocoee
  • Regeneron Study Site - Orlando

Arizona

  • Regeneron Study Site - Glendale
  • Regeneron Study Site - Glendale
  • Regeneron Study Site - Phoenix
  • Regeneron Study Site - Tucson

Texas

  • Regeneron Study Site - Bellaire
  • Regeneron Study Site - Houston
  • Regeneron Study Site - Houston

Illinois

  • Regeneron Study Site - Chicago
  • Regeneron Study Site - Chicago

Ohio

  • Regeneron Study Site - Cincinnati
  • Regeneron Study Site - Columbus

California

  • Regeneron Study Site - Anaheim

Georgia

  • Regeneron Study Site - Woodstock

Michigan

  • Regeneron Study Site - Caro

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2018-10-15
Est. Completion 2021-01-07
Phase Phase 2
Regeneron Pharmaceuticals

280 total trials

What the finished NCT03691974 record still lists

NCT03691974 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, below the 496-participant average among 112 other Osteoarthritis, Knee trials with a reported enrollment target (64% lower).

The record links to 2 conditions, with Osteoarthritis, Knee appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT03691974 names 20 study sites across 9 states, led by Florida, Arizona, Texas.

Frequently Asked Questions

What is clinical trial NCT03691974 about?

NCT03691974 is a clinical study titled "Study to Evaluate the Effects of Fasinumab on Peripheral Nerve Function in Patients With Pain Due to Osteoarthritis of the Hip or Knee". The primary objective of the study is to evaluate the effect of fasinumab compared to placebo on peripheral nerves in participants with pain due to Osteoarthritis (OA) of the hip or knee. The secondary objectives of the study are to: * Evaluate the efficacy of fasinumab compared to placebo in part...

What is the current status of trial NCT03691974?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 180 participants. The study started on 2018-10-15. Estimated completion is 2021-01-07.

What conditions does trial NCT03691974 study?

This clinical trial studies the following conditions: Osteoarthritis, Knee, Osteoarthritis, Hip.

What interventions are being tested in trial NCT03691974?

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

Who is sponsoring clinical trial NCT03691974?

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

Where is trial NCT03691974 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Osteoarthritis, Knee

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03691974's enrollment target sits among peer trials

180 37th of 112 higher than 75 of 112 other Osteoarthritis, Knee trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Osteoarthritis, Knee 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 NCT03691974, the US trial registry maintained by the National Library of Medicine. NCT03691974 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.