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Terminated Phase 2Phase 3 Interventional Results available

Study to Assess the Efficacy and Safety of VX-210 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

ClinicalTrials.gov ID: NCT02669849

Public ClinicalTrials.gov record NCT02669849. 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, 2:22 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 Phase 2b/3, Double-blind, Randomized, Placebo Controlled, Multicenter Study to Assess the Efficacy and Safety of VX-210 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

Brief summary

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

The purpose of this study is to determine the efficacy and safety of VX-210 in subjects with Acute Traumatic Cervical Spinal Cord Injury. Secondary objectives include the specific evaluation of the effects of VX-210 on neurological recovery and daily function after spinal cord injury.

Study identification

NCT ID
NCT02669849
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Enrollment
70 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
14 Years to 75 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 2016 (Actual)
Primary completion
Nov 2018 (Actual)
Completion
Nov 2018 (Actual)
Last update posted
Jan 22, 2020

2016 – 2018

United States locations

U.S. sites
33
U.S. states
22
U.S. cities
33
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Tucson Arizona — —
Not listed Fresno California — —
Not listed Orange California — —
Not listed Sacramento California — —
Not listed Jacksonville Florida — —
Not listed Tampa Florida — —
Not listed Atlanta Georgia — —
Not listed Savannah Georgia — —
Not listed Iowa City Iowa — —
Not listed Louisville Kentucky — —
Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
Not listed Ann Arbor Michigan — —
Not listed Minneapolis Minnesota — —
Not listed Jackson Mississippi — —
Not listed St Louis Missouri — —
Not listed Albuquerque New Mexico — —
Not listed Columbus Ohio — —
Not listed Toledo Ohio — —
Not listed Oklahoma City Oklahoma — —
Not listed Hershey Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Providence Rhode Island — —
Not listed Austin Texas — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Salt Lake City Utah — —
Not listed Falls Church Virginia — —
Not listed Richmond Virginia — —
Not listed Roanoke Virginia — —
Not listed Seattle Washington — —

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 NCT02669849, 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 Jan 22, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02669849 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →