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Clinical trialNCT01074008CompletedPhase 2Interventional

A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity of ABT-450, ABT-333 and ABT-072

SponsorAbbVie (prior sponsor, Abbott)Enrollment74Chronic Hepatitis C InfectionHCVHepatitis CHepatitis C Genotype 1
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

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

Puerto Rico
  • Site Reference Id/investigator# 23363

    Ponce, Puerto Rico

United States
  • Site Reference Id/investigator# 23392

    Phoenix, Arizona, United States

  • Site Reference Id/investigator# 23370

    Anaheim, California, United States

  • Site Reference Id/investigator# 23387

    La Jolla, California, United States

  • Site Reference Id/investigator# 23388

    Los Angeles, California, United States

  • Site Reference Id/investigator# 23371

    Aurora, Colorado, United States

  • Site Reference Id/investigator# 23369

    Orlando, Florida, United States

  • Site Reference Id/investigator# 26362

    Orlando, Florida, United States

  • Site Reference Id/investigator# 23373

    Chicago, Illinois, United States

  • Site Reference Id/investigator# 24908

    Chicago, Illinois, United States

  • Site Reference Id/investigator# 23381

    Indianapolis, Indiana, United States

  • Site Reference Id/investigator# 23372

    Baton Rouge, Louisiana, United States

  • Site Reference Id/investigator# 24710

    New Orleans, Louisiana, United States

  • Site Reference Id/investigator# 23391

    Baltimore, Maryland, United States

  • Site Reference Id/investigator# 23377

    Detroit, Michigan, United States

  • Site Reference Id/investigator# 24909

    Saint Paul, Minnesota, United States

  • Site Reference Id/investigator# 23379

    New York, New York, United States

  • Site Reference Id/investigator# 35842

    New York, New York, United States

  • Site Reference Id/investigator# 23375

    Chapel Hill, North Carolina, United States

  • Site Reference Id/investigator# 23385

    Durham, North Carolina, United States

  • Site Reference Id/investigator# 23376

    Dallas, Texas, United States

  • Site Reference Id/investigator# 24891

    Houston, Texas, United States

  • Site Reference Id/investigator# 23382

    San Antonio, Texas, United States

  • Site Reference Id/investigator# 24715

    Salt Lake City, Utah, United States

  • Site Reference Id/investigator# 25463

    Seattle, Washington, United States

  • Site Reference Id/investigator# 23383

    Madison, Wisconsin, 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
31 Mar 2010
Primary completion
30 Jun 2011
Completion
31 Jan 2012
Last update posted
8 Jan 2015
Registered enrollment
74
Registry id
NCT01074008

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.