drugset / Trial / NCT05192200

An Extension Study for Participants Who Have Completed the Treatment Period of a Qualifying Parent Study

NCT05192200 ↗

Phase 2 Completed 24 enrolled Pfizer
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this research study is to evaluate the long-term safety, and tolerability of PF-06823859 study drug in adult participants with Dermatomyositis (DM) from a qualifying study.

Timeline

Start
2021-12-20
Primary completion
2023-11-20
Completion
2023-11-20

Drugs

EvaluationDrugModalityDoseRoute
Subject dazukibart Monoclonal antibody — Intravenous

Indications