drugset / Trial / NCT04534842

Efficacy and Safety of SYNB1618 and SYNB1934 in Adult Patients With Phenylketonuria

NCT04534842 ↗

Phase 2 Completed 20 enrolled Synlogic
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This Phase 2 study in patients with phenylketonuria (PKU) will be an open-label, dual-arm study of either a SYNB1618 or SYNB1934 dose-ramp regimen. All evaluations and assessments throughout this study may be conducted either at the clinical site or by a home healthcare professional at an alternative location (e.g., patient's home, hotel).

Timeline

Start
2020-08-25
Primary completion
2022-10-07
Completion
2022-10-07

Drugs

EvaluationDrugModalityDoseRoute
Subject LABAFENOGENE MARSELECOBAC Cell therapy — Oral
Subject SYNB1618 Other / unclassified — Oral

Indications