A PHASE 3, MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PF-06823859 IN PARTICIPANTS WITH ACTIVE IDIOPATHIC INFLAMMATORY MYOPATHIES (INCLUDING PARTICIPANTS WITH ACTIVE DERMATOMYOSITIS OR POLYMYOSITIS)
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- Pfizer
- 入组人数
- 318
- 试验地点
- 253
- 主要终点
- Moderate change in Total Improvement Score (TIS)
研究概览
简要总结
The purpose of the study is to understand how the study medicine PF-06823859 (dazukibart) works in people with idiopathic inflammatory myopathies (DM and PM). These disorders cause inflammation that weakens the muscles that are important for movement and may also cause skin rash in people with DM.
This study is seeking participants who:
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Are 18 years of age or older or minimum legal adult age as defined per local regulation, whichever is greater
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Have active DM or active PM.
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Are receiving a stable dose of 1 corticosteroid taken by mouth and/or 1 traditional immunosuppressant.
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Note: Corticosteroids and immunosuppressants are medicines that help reduce inflammation and may signal to the immune system not to attack the body.
Dermatomyositis (DM) is a rare disease that causes muscle inflammation that results in muscle weakness and low muscle stamina. Patients with DM have a characteristic skin rash. Polymyositis (PM) is a rare disease that involves mainly muscle inflammation resulting in muscle weakness, that can sometimes be painful. Patients with DM and PM may have trouble going up the steps, walking or getting to a standing position.
Some of the participants will receive the study medicine (dazukibart) and some will receive placebo (which is similar to study medicine but contains no medicine in it).
The study medicine or placebo will be given as an intravenous (IV) infusion (directly into the veins), which takes about 1 hour; every 4 weeks from Day 1 to Week 48 of the study. Both dazukibart and placebo and will be given at the study site.
The study will compare the experiences of people receiving study medication to those of the people who do not. This will help to see if dazukibart is safe and effective.
Participants will take part in this study for about 13 months. During this time, participants will have 15 study visits. These visits will be performed at the study site.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
The sponsor, participants, and site personnel (including the investigator) will be masked to study treatment and will not know whether active study medication or placebo is being administered to participants.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female adults (≥18 years old or minimum legal adult age as defined per local regulation, whichever is greater)
- •Active dermatomyositis (DM) or polymyositis (PM) with age of onset
- •18 years old.
- •Must be receiving a stable dose of standard of care (SOC) background medications at the time of enrollment.
排除标准
- •Myositis due to non-Idiopathic inflammatory myopathies (non-IIM)
- •Existing diagnosis of inclusion body myositis (IBM)
- •Presence of immune-mediated necrotizing myositis (IMNM)
- •Myositis with end-stage organ involvement
- •Active bacterial, viral or fungal infections or hospitalizations for serious infections within 60 days prior to enrollment
- •History of recurrent bacterial, viral, fungal, mycobacterial or other infections
- •Clinically significant finding on a chest x-ray
- •Have cancer or a history of cancer within 5 years of screening
- •Significant current or prior disease conditions that may interfere with the response to or safety of the study medicine, including but not limited to:
- •history of major organ transplant
- •acute coronary syndrome or any history of significant cerebrovascular disease within 24 weeks of screening
- •preexisting demyelinating disorder such as multiple sclerosis, or other severe neurological disorder
- •major surgery within 4 weeks of screening, or scheduled to occur during the study, excluding diagnostic surgery
- •previous treatment with total lymphoid irradiation
- •history of any lymphoproliferative disorder such as Epstein Barr Virus, history of lymphoma, leukemia, or symptoms of current lymphatic or lymphoid disease
- •Clinically significant depression, suicidal ideation, or previous history of suicidal behaviors
- •Other medical or laboratory abnormality that may increase the risk of study participation
- •Previous administration with an investigational product (drug or vaccine) within 30 days or of the first dose of study medicine
- •Current use or incomplete appropriate washout period of any prohibited medication(s) or known exposure to anti-interferon beta (PF-06823859) or any type of anti-interferon beta therapy
- •Prior SOC medication that does not fulfill the criteria
- •Certain laboratory results from screening assessments that may interfere with study participation.
- •Investigator site staff directly involved in the conduct of the study and their family members, site staff and sponsor and sponsor delegate employees directly involved in the conduct of the study and their family members
研究组 & 干预措施
Placebo
Participants will receive placebo via intravenous infusion every 4 weeks.
干预措施: Placebo (Drug)
PF-06823859
Participants will receive PF-06823859 via intravenous infusion every 4 weeks.
干预措施: PF-06823859 (Drug)
结局指标
主要结局
Moderate change in Total Improvement Score (TIS)
时间窗: 24 weeks outside of the United States (US) and 52 weeks in the US
Total Improvement Score 0 to 100 with higher scores indicating a better outcome.
次要结局
- Corticosteroid (CS) dose assessment(52 weeks)
- Change from baseline in Manual Muscle Testing - 8 designated muscles (MMT-8)(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in Cutaneous Dermatomyositis Disease Area and Severity Index Activity Score (CDASI-A) in participants with dermatomyositis (DM)(Week 24 outside the US)
- Change from baseline in Investigator Global Assessment severity scale (IGA) in participants with dermatomyositis(24 and 52 weeks in the US only)
- Moderate change in Total Improvement Score(24 weeks in the US and 52 weeks outside of the US)
- Change from baseline in Patient-Reported Outcomes Measurement Information System - Physical Function (PROMIS-PF)(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in 5-D Itch Scale Score(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F)(24 weeks outside of the US and 52 weeks in the US)
- Response in corticosteroid tapering(52 weeks US only)
- Change from baseline in Manual Muscle Testing - 8 designated muscles (MMT-8)(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in Cutaneous Dermatomyositis Disease Area and Severity Index Activity Score (CDASI-A) in participants with dermatomyositis (DM)(Week 24 outside the US)
- Change from baseline in Investigator Global Assessment severity scale (IGA) in participants with dermatomyositis(24 and 52 weeks in the US only)
- Corticosteroid (CS) dose assessment(52 weeks)
- Moderate change in Total Improvement Score(24 weeks in the US and 52 weeks outside of the US)
- Change from baseline in Patient-Reported Outcomes Measurement Information System - Physical Function (PROMIS-PF)(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in 5-D Itch Scale Score(24 weeks outside of the US and 52 weeks in the US)
- Change from baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F)(24 weeks outside of the US and 52 weeks in the US)
- Response in corticosteroid tapering(52 weeks US only)