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NCT02207725 · ClinicalTrials.gov registry record · Phase 3

A Study in Older Subjects to Evaluate the Safety and Ability of Andexanet Alfa to Reverse the Anticoagulation Effect of Apixaban

A Phase 3 study, sponsored by Portola Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
68
Enrollment target

NCT02207725: Completed Phase 3 study, sponsored by Portola Pharmaceuticals.

NCT02207725 is a Phase 3 study that has completed, run by Portola Pharmaceuticals. The registered enrollment target is 68 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02207725, a Phase 3 study, has completed, sponsored by Portola Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
68 participants
Enrollment target

Study Summary

The purpose of this stuy is to evaluate the ability of Andexanet Alfa to reverse the anticoagulation effect of Apixaban.

Primary Outcome

In Part I, the primary endpoint was percent change from baseline in anti-fXa activity at the nadir, when nadir was defined as the smaller value for anti-fXa activity at the +2 minutes or +5 minutes time point following the end of the bolus. In Part II, the primary endpoint was the percent change from baseline in anti-fXa activity from its baseline to nadir, when nadir was defined as the smaller value for anti-fXa activity between the 110-minute time point (10 minutes prior to the end of the cont

Interventions

  • OTHER Placebo
  • BIOLOGICAL Andexanet

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2014-03
Est. Completion 2015-09
Phase Phase 3
Portola Pharmaceuticals

13 total trials

What the finished NCT02207725 record still lists

NCT02207725 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02207725 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02207725 about?

NCT02207725 is a clinical study titled "A Study in Older Subjects to Evaluate the Safety and Ability of Andexanet Alfa to Reverse the Anticoagulation Effect of Apixaban". The purpose of this stuy is to evaluate the ability of Andexanet Alfa to reverse the anticoagulation effect of Apixaban.

What is the current status of trial NCT02207725?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 68 participants. The study started on 2014-03. Estimated completion is 2015-09.

What interventions are being tested in trial NCT02207725?

The interventions under investigation include: Placebo (OTHER), Andexanet (BIOLOGICAL).

Who is sponsoring clinical trial NCT02207725?

This trial is sponsored by Portola Pharmaceuticals, which has 13 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02207725's enrollment target sits among peer trials

68 1796th of 2000 higher than 205 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT02207725, the US trial registry maintained by the National Library of Medicine. NCT02207725 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.