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Clinical trialNCT01830985CompletedPhase 2/PHASE3Interventional

A Phase 2/3 Open-label Extension Study to Evaluate Long-Term Safety and Efficacy With VX-509 in Subjects With Rheumatoid Arthritis

SponsorVertex Pharmaceuticals IncorporatedEnrollment39Rheumatoid Arthritis
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

22 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Estonia
  • Vertex Investigational Site

    Tallinn, Estonia

Lithuania
  • Vertex Investigational Site

    Vilnius, Lithuania

South Africa
  • Vertex Investigational Site

    Pretoria, South Africa

  • Vertex Investigational Site

    Stellenbosch, South Africa

United States
  • Vertex Investigational Site

    Upland, California, United States

  • Vertex Investigational Site

    Fort Lauderdale, Florida, United States

  • Vertex Investigational Site

    Venice, Florida, United States

  • Vertex Investigational Site

    West Palm Beach, Florida, United States

  • Vertex Investigational Site

    Canton, Georgia, United States

  • Vertex Investigational Site

    Decatur, Georgia, United States

  • Vertex Investigational Site

    Elizabethtown, Kentucky, United States

  • Vertex Investigational Site

    Fredrick, Maryland, United States

  • Vertex Investigational Site

    Lincoln, Nebraska, United States

  • Vertex Investigational Site

    Rochester, New York, United States

  • Vertex Investigational Site

    Greensboro, North Carolina, United States

  • Vertex Investigational Site

    Duncansville, Pennsylvania, United States

  • Vertex Investigational Site

    Charleston, South Carolina, United States

  • Vertex Investigational Site

    Memphis, Tennessee, United States

  • Vertex Investigational Site

    Katy, Texas, United States

  • Vertex Investigational Site

    San Antonio, Texas, United States

  • Vertex Investigational Site

    Webster, Texas, United States

  • Vertex Investigational Site

    Spokane, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Apr 2013
Primary completion
31 Jul 2014
Completion
31 Jul 2014
Last update posted
20 Nov 2015
Registered enrollment
39
Registry id
NCT01830985

Cross-registrations

EU-CTR / CTIS (EudraCT)2012-004342-14

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.