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Clinical Trial Summary

The purpose of this study is to determine the efficacy, durability and long-term safety of reloxaliase in patients with enteric hyperoxaluria.


Clinical Trial Description

This is a phase 3, global, multi-center, randomized, double-blind, placebo-controlled study. This study is designed to determine the short- and long-term efficacy of reloxaliase in terms of reducing urinary oxalate excretion and clinical benefits compared to placebo. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03847090
Study type Interventional
Source Allena Pharmaceuticals
Contact
Status Terminated
Phase Phase 3
Start date August 26, 2019
Completion date May 19, 2022

See also
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Completed NCT05377112 - Safety, Tolerability, and Pharmacodynamics of SYNB8802v1 in Subjects With History of Gastric Bypass Surgery or Short-bowel Syndrome Early Phase 1
Terminated NCT04909723 - Safety, Tolerability, and Pharmacodynamics of NOV-001 in Adult Subjects Phase 1/Phase 2
Completed NCT03391804 - Study of ALLN-177 in Patients Aged 12 Years or Older With Enteric or Primary Hyperoxaluria and Hyperoxalemia Phase 2
Completed NCT00588120 - Enteric Oxalate Absorption Study in Unclassified Hyperoxaluria Phase 1