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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 Jul 21, 2026, 4:43 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

Study identification

NCT ID
NCT02669849
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Vertex Pharmaceuticals Incorporated
Industry
Enrollment
70 participants

Conditions and interventions

Interventions

  • VX-210 Drug
  • Placebo Drug

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
Jun 30, 2016
Primary completion
Oct 31, 2018
Completion
Oct 31, 2018
Last update posted
Jan 21, 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 21, 2020 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT02669849 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →