drugset / Trial / NCT01042678

Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema

NCT01042678 ↗

Phase 1 Terminated 18 enrolled Allergan Molecular Partners AG · collab
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of MP0112 (a novel, potentially long acting VEGF inhibitor) in patients with diabetic retinal edema.

Timeline

Start
2010-02
Primary completion
2010-12
Completion
2010-12

Outcome

Outcome not reported

Stopped: “The study was terminated due to a company decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Abicipar pegol Protein / enzyme biologic 0.04 mg Intravitreal
Subject Abicipar pegol Protein / enzyme biologic 0.15 mg Intravitreal
Subject Abicipar pegol Protein / enzyme biologic 0.4 mg Intravitreal
Subject Abicipar pegol Protein / enzyme biologic 1 mg Intravitreal
Subject Abicipar pegol Protein / enzyme biologic 2 mg Intravitreal
Subject Abicipar pegol Protein / enzyme biologic 3.6 mg Intravitreal