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NCT02823964 · ClinicalTrials.gov registry record · Phase 4

EASY: Extended Access to Sollpura Over Years

A Phase 4 study, sponsored by Anthera Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
25
Enrollment target

NCT02823964: Completed Phase 4 study, sponsored by Anthera Pharmaceuticals.

NCT02823964 is a Phase 4 study that has completed, run by Anthera Pharmaceuticals. The registered enrollment target is 25 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02823964, a Phase 4 study, has completed, sponsored by Anthera Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
25 participants
Enrollment target

Study Summary

Liprotamase consists of 3 soluble, non-porcine digestive enzymes, lipase, protease, and amylase, combined in a fixed ratio. Liprotamase is stable in the stomach and can be formulated without enteric coating for administration either as a capsule or as a dosing solution dissolved in water or juice.

Primary Outcome

Descriptive analysis

Interventions

  • DRUG Liprotamase

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2016-09
Est. Completion 2018-03
Phase Phase 4
Anthera Pharmaceuticals

16 total trials

What the finished NCT02823964 record still lists

NCT02823964 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Liprotamase is the first listed.

NCT02823964 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02823964 about?

NCT02823964 is a clinical study titled "EASY: Extended Access to Sollpura Over Years". Liprotamase consists of 3 soluble, non-porcine digestive enzymes, lipase, protease, and amylase, combined in a fixed ratio. Liprotamase is stable in the stomach and can be formulated without enteric coating for administration either as a capsule or as a dosing solution dissolved in water or juice.

What is the current status of trial NCT02823964?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 25 participants. The study started on 2016-09. Estimated completion is 2018-03.

What interventions are being tested in trial NCT02823964?

The interventions under investigation include: Liprotamase (DRUG).

Who is sponsoring clinical trial NCT02823964?

This trial is sponsored by Anthera Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02823964's enrollment target sits among peer trials

25 1669th of 2000 higher than 302 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02823964, the US trial registry maintained by the National Library of Medicine. NCT02823964 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.