RecruitingPhase 3NCT06698796

A Study to Understand How the Study Medicine Dazukibart Works in People With Idiopathic Inflammatory Myopathies

A PHASE 3, MULTI-CENTER, OPEN-LABEL EXTENSION STUDY TO INVESTIGATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF DAZUKIBART IN PARTICIPANTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES (INCLUDING PARTICIPANTS WITH DERMATOMYOSITIS OR POLYMYOSITIS)


Sponsor

Pfizer

Enrollment

211 participants

Start Date

Jan 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to understand how the study medicine, dazukibart, works in people with active idiopathic inflammatory myopathies (dermatomyositis \[DM\] or polymyositis \[PM\]). Idiopathic inflammatory myopathies are a group of disorders that show inflammation of the muscles used for movement. There are several types of idiopathic inflammatory myopathies, including DM and PM. DM and PM involve weakness of the muscles closest to the center of the body, such as the muscles of the hips, thighs, upper arms, and neck. People with these forms of idiopathic inflammatory myopathies may find it difficult to climb stairs, get up from a seated position, or lift items above their head. People with DM can also have a skin rash. These disorders negatively impact the quality of life and functioning of patients. In addition to the above, these disorders can affect how the lungs and heart work. This study is seeking participants who took part in a DM and PM study with dazukibart before. Some participants will receive study medicine, and some participants will not receive study medicine and only complete safety follow-up. The study medicine will be given as an intravenous (IV) infusion (directly into the veins). This takes about 1 hour, every 4 weeks, from Day 1 to Week 48 (about 12 months) of the study. This will be followed by a safety follow-up period that lasts about 4 months after the last infusion. Participants who receive study medicine will have about 18 study visits at the site over about 16 months. There will also be participants enrolled in this study who will not receive study medicine. Such participants will only take part in safety follow-up visits as they do not want to or are not eligible to receive dazukibart. These participants will not receive study medicine and will have up to 4 study visits at the site every 4 weeks to complete safety follow-up.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • Participants that completed a qualifying study through Week 52.

Exclusion Criteria6

  • Any medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation.
  • Previous administration with an investigational product (drug or vaccine) other than dazukibart in a qualifying study within 30 days (or as determined by the local requirement) or 5 half-lives preceding baseline in this study (whichever is longer).
  • Current use of any prohibited concomitant medication(s).
  • Active bacterial, viral, fungal, mycobacterial or other infections.
  • Ongoing adverse event in a qualifying study or the participant has met safety monitoring criteria in a qualifying study that have not resolved.
  • Investigator site staff or sponsor employees directly involved in the conduct of the study, site staff otherwise supervised by the investigator, and their respective family members.

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Interventions

DRUGDazukibart

anti-interferon beta therapy


Locations(22)

AARA Clinical Research - Arizona Arthritis & Rheumatology Associates - Glendale

Glendale, Arizona, United States

Arthritis & Rheumatology Research Institute, PLLC

Allen, Texas, United States

Nerve & Muscle Center of Texas

Houston, Texas, United States

Rheumatology & Pulmonary Clinic

Beckley, West Virginia, United States

Centro de Investigaciones Médicas Tucuman

SAN M. de Tucuman, Tucumán Province, Argentina

Medical Center Artmed

Plovdiv, Bulgaria

Anhui Provincial Hospital

Hefei, Anhui, China

The Second Affiliated Hospital of Nanchang University

Nanchang, Jiangxi, China

Renji Hospital Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China

Renji Hospital Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China

First Affiliated Hospital of Kunming Medical University

Kunming, Yunnan, China

Peking Union Medical College Hospital

Beijing, China

Debreceni Egyetem Klinikai Kozpont

Debrecen, Hungary

CHARM HEALTHCARE PRIVATE LIMITED (Previously Dr Shenoy's Care Private Limited)

Ernākulam, Kerala, India

Sheba Medical Center

Ramat Gan, Central District, Israel

Institute of Science Tokyo Hospital

Bunkyo-ku, Tokyo, Japan

Nippon Medical School Hospital

Bunkyo-ku, Tokyo, Japan

Cryptex Investigación Clínica S.A. de C.V.

Cuauhtémoc, Mexico City, Mexico

Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji

Warsaw, Masovian Voivodeship, Poland

Nova Reuma Domyslawska i Rusilowicz Spolka Partnerska Lekarza Reumatologa i Fizjoterapeuty

Bialystok, Podlaskie Voivodeship, Poland

National Taiwan University Hospital

Taipei, Taiwan

Hacettepe Universite Hastaneleri

Altindağ, Ankara, Turkey (Türkiye)

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NCT06698796


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