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NCT02232178 · ClinicalTrials.gov registry record · Phase 2

Pharmacokinetics, Relative Bioavailability and Safety of Xaracoll Implant

A Phase 2 study, sponsored by Innocoll.

Completed
Registry status
Phase 2
Development phase
64
Enrollment target

NCT02232178: Completed Phase 2 study, sponsored by Innocoll.

NCT02232178 is a Phase 2 study that has completed, run by Innocoll. The registered enrollment target is 64 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (52% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02232178, a Phase 2 study, has completed, sponsored by Innocoll.

COMPLETED
Registry status
Phase 2
Development phase
64 participants
Enrollment target

Study Summary

Assess the pharmacokinetic profile of 2 doses of the XaraColl® implant after open laparotomy hernioplasty and assess the relative bioavailability of Xaracoll compared to a local bupivacaine infiltration.

Primary Outcome

Maximum drug plasma concentration

Interventions

  • DRUG 2 100mg Xaracoll implants
  • DRUG 3 100mg Xaracoll implants
  • DRUG 150mg Bupivacaine HCl injection

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2014-10-20
Est. Completion 2015-03-23
Phase Phase 2
Innocoll

19 total trials

What the finished NCT02232178 record still lists

NCT02232178 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (52% lower).

The record links to 0 conditions, and to 3 interventions - of which 2 100mg Xaracoll implants is the first listed.

NCT02232178 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02232178 about?

NCT02232178 is a clinical study titled "Pharmacokinetics, Relative Bioavailability and Safety of Xaracoll Implant". Assess the pharmacokinetic profile of 2 doses of the XaraColl® implant after open laparotomy hernioplasty and assess the relative bioavailability of Xaracoll compared to a local bupivacaine infiltration.

What is the current status of trial NCT02232178?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 64 participants. The study started on 2014-10-20. Estimated completion is 2015-03-23.

What interventions are being tested in trial NCT02232178?

The interventions under investigation include: 2 100mg Xaracoll implants (DRUG), 3 100mg Xaracoll implants (DRUG), 150mg Bupivacaine HCl injection (DRUG).

Who is sponsoring clinical trial NCT02232178?

This trial is sponsored by Innocoll, which has 19 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02232178's enrollment target sits among peer trials

64 996th of 2000 higher than 992 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 NCT02232178, the US trial registry maintained by the National Library of Medicine. NCT02232178 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.