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NCT01221298 · ClinicalTrials.gov registry record · Phase 2

A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of ABT-450 With Ritonavir (ABT-450/r) Dosed in Combination With ABT-072 and Ribavirin (RBV)

A Phase 2 study, sponsored by AbbVie (prior sponsor, Abbott).

Completed
Registry status
Phase 2
Development phase
11
Enrollment target

NCT01221298: Completed Phase 2 study, sponsored by AbbVie (prior sponsor, Abbott).

NCT01221298 is a Phase 2 study that has completed, run by AbbVie (prior sponsor, Abbott). The registered enrollment target is 11 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01221298, a Phase 2 study, has completed, sponsored by AbbVie (prior sponsor, Abbott).

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and antiviral activity of ABT-450 with ritonavir (ABT-450/r) dosed in combination with ABT-072 and ribavirin (RBV) in treatment-naïve participants with genotype 1 chronic hepatitis C virus (HCV) infection.

Primary Outcome

Analysis of the percentage of participants with hepatitis C virus ribonucleic acid less than the lower limit of quantitation (\< 25 IU/mL).

Interventions

  • DRUG Ritonavir
  • DRUG Ribavirin
  • DRUG ABT-072
  • DRUG ABT-450

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2010-10
Est. Completion 2012-04
Phase Phase 2
AbbVie (prior sponsor, Abbott)

88 total trials

What the finished NCT01221298 record still lists

NCT01221298 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 4 interventions - of which Ritonavir is the first listed.

NCT01221298 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01221298 about?

NCT01221298 is a clinical study titled "A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of ABT-450 With Ritonavir (ABT-450/r) Dosed in Combination With ABT-072 and Ribavirin (RBV)". The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and antiviral activity of ABT-450 with ritonavir (ABT-450/r) dosed in combination with ABT-072 and ribavirin (RBV) in treatment-naïve participants with genotype 1 chronic hepatitis C virus (HCV) infection.

What is the current status of trial NCT01221298?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2010-10. Estimated completion is 2012-04.

What interventions are being tested in trial NCT01221298?

The interventions under investigation include: Ritonavir (DRUG), Ribavirin (DRUG), ABT-072 (DRUG), ABT-450 (DRUG).

Who is sponsoring clinical trial NCT01221298?

This trial is sponsored by AbbVie (prior sponsor, Abbott), which has 88 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01221298's enrollment target sits among peer trials

11 1967th of 2000 higher than 33 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01221298, the US trial registry maintained by the National Library of Medicine. NCT01221298 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.