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NCT00418795

Porphozym in the Treatment of Acute Attacks in AIP

Completed Phase 2, PHASE3 Last updated 9 March 2018
What this trial tests

Phase 2, PHASE3 trial testing recombinant human porphobilinogen deaminase (Porphozym) in Acute Intermittent Porphyria in 36 participants. Completed in 20 June 2006.

Timeline
11 June 2003
Primary endpoint
20 June 2006
20 June 2006

Quick facts

Lead sponsorZymenex A/S
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment36
Start date11 June 2003
Primary completion20 June 2006
Estimated completion20 June 2006
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Zymenex A/S — full company profile →

Who can join

18 and older, any sex, with Acute Intermittent Porphyria. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A multi-centre, double-blind, randomized, placebo controlled, parallel group trial, investigating the efficacy and safety of Porphozym (recombinant human porphobilinogen deaminase)in the treatment of acute attacks in AIP.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Acute Intermittent Porphyria

Currently open trials in the same condition.

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Data sources for this page

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