M281
DrugM281 injection administered as intravenous infusion
Other names: Nipocalimab, JNJ-80202135
NCT Number: NCT04119050
The main purpose of this study is to evaluate the efficacy and safety of M281 in participants with warm autoimmune hemolytic anemia (wAIHA).
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Hospital das Clínicas da Faculdade de Medicina de Botucatu, Botucatu, Brazil
The study consists of a 24-week double-blind, placebo control period, a 144-week open-label extension period and follow-up period of 8 weeks after last study drug administration. Eligible participants will be randomized to placebo or nipocalimab (2 dose levels) during the double-blind period and nipocalimab (2 dose levels) during the open-label extension period.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
M281 injection administered as intravenous infusion
Other names: Nipocalimab, JNJ-80202135
Placebo administered as intravenous infusion
Time frame: Up to Week 20 of the double-blind period
Time frame: Baseline (Day 1, Week 0) through Week 24
The FACIT-Fatigue is a self-administered 13-item questionnaire that assess patient-reported fatigue associated with chronic illness therapy. It assesses both the physical and functional consequences of fatigue. Each question is answered on a 5-point scale, where 0 means "not at all," and 4 means "very much." The FACIT-Fatigue scale score ranges from 0 to 52, with higher scores denoting lower levels of fatigue. A positive change from baseline score indicates an improvement.
Time frame: Baseline (Day 1, Week 0) through Week 24 of the double-blind period
The FACIT-Fatigue is a self-administered 13-item questionnaire that assess patient-reported fatigue associated with chronic illness therapy. It assesses both the physical and functional consequences of fatigue. Each question is answered on a 5-point scale, where 0 means "not at all," and 4 means "very much." The FACIT-Fatigue scale score ranges from 0 to 52, with higher scores denoting lower levels of fatigue. A positive change from baseline score indicates an improvement.
Time frame: Baseline (Day 1, Week 0) and at Week 24
Change from baseline in average daily dose of prednisone or equivalent at week 24 among participants on prednisone or equivalent at baseline will be reported.
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Up to 24 weeks
Percentage of participants who achieve the durable response in improvement of Hgb during the double-blind period and maintain that response for up to 24 weeks, without the need of rescue therapy will be reported.
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24
Time frame: Baseline (Day 1, Week 0) through Week 24 of the double-blind period
The FACIT-Fatigue scale is a 13-item self-administered questionnaire that assesses both the physical and functional consequences of fatigue. Each question is answered on a 5-point scale, where 0 means "not at all," and 4 means "very much." The FACIT-Fatigue scale score ranges from 0 to 52, with higher scores denoting lower levels of fatigue. A positive change from baseline score indicates an improvement.
Time frame: Baseline (Day 1, Week 0) through Week 24
The EQ-5D-5L quality of life questionnaire will be used to assess health related quality of life status. The 5 dimensions are mobility, self-care, usual activities, pain/discomfort, and anxiety/depression; each dimension is rated by the patient on a 5 level scale (no problems, slight problems, moderate problems, severe problems, extreme problems).
Time frame: Baseline (Day 1, Week 0) through Week 24
The SF-36v2 will be used to assess general quality of life. The 36 items on the SF-36 health survey encompass the following 8 domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. The 8 domains can be aggregated into 2 summary scales that reflect physical and mental health: a physical component summary (PCS) and a mental component summary (MCS). Responses to all items are rated on a 3-, 5- or 6-point Likert scale. Higher scores indicate a higher level of functioning. A positive change from baseline score indicates an improvement.
Time frame: Baseline (Day 1, Week 0) through Week 24
The PGIS will be used to assess the severity of warm autoimmune hemolytic anemia (wAIHA) fatigue symptoms. The PGIS is a 5-point response scale. Participant will be asked to rate their fatigue over the past 7 days using the following 5-point scale: 1 = None, 2 = Mild, 3 = Moderate, 4 = Severe, and 5 = Very severe.
Time frame: At Week 24
The PGIC will assess if there has been an improvement or decline in patient-reported status since the beginning of the treatment. The PGIC is a 7-point response scale. Participants will be asked to rate their current fatigue as compared to when they started the study, using the following 7-point scale: 1 = Much better, 2 = Moderately better, 3 = A little better, 4 = No change, 5 = A little worse, 6 = Moderately worse, and 7 = Much worse.
Time frame: Baseline (Day 1, Week 0) through Week 24
It will be estimated using a model-based longitudinal analysis of Hgb/hemolysis parameters in relationship to IgG level and dose regimen.
Time frame: Baseline (Day 1, Week 0) and at Week 24
Absolute change from baseline in average daily dose of prednisone or equivalent at Week 24 among all participants will be reported.
Time frame: At Week 24
Percentage of participants who achieve corticosteroid reduction to <= 7.5 mg/day of oral prednisone (or equivalent) at Week 24 of the double-blind period, among participants with prednisone or equivalent >7.5 mg/day at baseline will be reported.
Janssen Research & Development, LLC
Industry
Efficacy and Safety of M281 in Adults With Warm Autoimmune Hemolytic Anemia: A Multicenter, Randomized, Double-blind, Placebo-controlled Study With a Long-term Open-label Extension
Acronym: ENERGY
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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