drugset / Trial / NCT05641324

A Study of ANV419 Alone or in Combination With Approved Treatments in Patients With Multiple Myeloma (OMNIA-2)

NCT05641324 ↗

Phase 1 Terminated 4 enrolled Anaveon AG
RandomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of ANV419 monotherapy followed by ANV419 in combination with lenalidomide plus low-dose dexamethasone or ANV419 in combination with daratumumab.

Timeline

Start
2023-02-10
Primary completion
2023-07-12
Completion
2023-07-12

Outcome

Outcome not reported

Stopped (Enrollment): “The study was ended due to a lack of recruitment”

Drugs

EvaluationDrugModalityDoseRoute
Subject ANV419 Protein / enzyme biologic — Intravenous
Subject Daratumumab Monoclonal antibody — Subcutaneous
Subject Dexamethasone Small molecule — Oral
Subject Lenalidomide Other / unclassified — Oral

Indications