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DermatomyositisPhase 2/3NCT04999020

Ravulizumab Versus Placebo in Adult Participants With Dermatomyositis

A Phase 2/3 study testing Ravulizumab in people with Dermatomyositis, run by Alexion Pharmaceuticals, Inc. at 111 sites in 13 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

Trial summary

This is a Phase 2/3, double-blind, randomized, placebo-controlled, parallel group, multicenter study to evaluate the efficacy, safety, pharmacokinetics, pharmacodynamics, and immunogenicity of ravulizumab in adult participants with dermatomyositis (DM). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Dermatomyositis
What is being tested?
Ravulizumab
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
38 participants
Where
111 sitesin 13 countries
Study dates
19 Nov 2021to 8 May 2024
Phase
Phase 2/3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 18 years of age or older at the time of signing the informed consent.
  • Body weight ≥ 30 kilograms at the time of Screening.
  • Male or female.
  • Diagnosis: Meet 2017 American College of Rheumatology/European League Against Rheumatism classification criteria for definite or probable DM.
  • Participants who have an inadequate response or are intolerant to 1 or more DM treatments, including systemic corticosteroids or immunosuppressive/immunomodulatory therapies (for example, azathioprine, methotrexate, rituximab, intravenous immunoglobulin), either in combination or as monotherapy.
  • Vaccinated against Neisseria meningitidis within 3 years prior to initiating ravulizumab as per national and local guidelines. Participants must receive the vaccination at least 2 weeks before first study intervention. The sponsor recommends that national and local guidelines for prophylactic antibiotics should also be followed.
  • Female participants of childbearing potential and male participants must follow specified contraception guidance as described in the protocol.

Who cannot join

  • Participants who have been diagnosed with cancer within the last 3 years need to have appropriate negative cancer screening as per local standard of care within 6 months before Screening (basal or squamous cell skin cancer or carcinoma in situ of the cervix needs to have been excised and without evidence of residual disease for at least 3 months before Screening).
  • Evidence of active malignant disease or malignancies diagnosed within the previous 3 years including hematological malignancies and solid tumors.
  • Participants with other forms of myositis.
  • As per investigator discretion, participants with significant muscle damage (for example, severe muscle atrophy, end stage muscle disease, MRI with severe atrophy or fibrofatty replacement)
  • History of Neisseria meningitidis infection.
  • Human immunodeficiency virus (HIV) infection (evidenced by HIV Type 1 or Type 2 antibody titer).
Show all 11Show fewer
  • Active systemic bacterial, viral, or fungal infection within 14 days prior to ravulizumab administration.
  • Presence of fever ≥ 38°Celsius (100.4°Fahrenheit) within 7 days prior to study drug administration on Day 1.
  • History of hypersensitivity to murine proteins or to 1 of the excipients of ravulizumab.
  • Pregnant, breastfeeding, or intending to conceive during the course of the study.
  • Inability or unwillingness to adhere to the protocol requirements.

Trial locations and contacts

111 sites in 13 countries.

111 sites in 13 countries

United States20 sites
  • Research Site

    Atlanta, Georgia, 30322

  • Research Site

    Baltimore, Maryland, 21205

  • Research Site

    Chapel Hill, North Carolina, 27599

  • Research Site

    Charleston, South Carolina, 29425

  • Research Site

    Chicago, Illinois, 60637

  • Research Site

    Cleveland, Ohio, 44195

  • Research Site

    Durham, North Carolina, 27710

  • Research Site

    Fairway, Kansas, 66205

  • Research Site

    Irvine, California, 92617

  • Research Site

    Las Vegas, Nevada, 89145

  • Research Site

    Manhasset, New York, 11030

  • Research Site

    Memphis, Tennessee, 38120

  • Research Site

    New York, New York, 10021

  • Research Site

    North Richland Hills, Texas, 76180

  • Research Site

    Phoenix, Arizona, 85032

  • Research Site

    Pittsburgh, Pennsylvania, 15213

  • Research Site

    Santa Monica, California, 90404

  • Research Site

    Seattle, Washington, 98122

  • Research Site

    Tampa, Florida, 33612

  • Research Site

    Washington D.C., District of Columbia, 20037

Other trials in United States

Italy19 sites
  • Research Site

    Bari, 70124

  • Research Site

    Brescia, 25123

  • Research Site

    Catania, 95123

  • Research Site

    Florence, 50134

  • Research Site

    Iesi, 60035

  • Research Site

    Messina, 98124

  • Research Site

    Milan, 20132

  • Research Site

    Pavia, 27100

  • Research Site

    Pisa, 56126

  • Research Site

    Reggio Emilia, 42122

  • Research Site

    Roma, 00128

  • Research Site

    Roma, 00168

  • Research Site

    Rome, 00189

  • Research Site

    Rozzano, 20089

  • Research Site

    Siena, 53100

  • Research Site

    Torino, 10126

  • Research Site

    Torrette AN, 60126

  • Research Site

    Udine, 33100

  • Research Site

    Verona, 37126

Other trials in Italy

Spain16 sites
  • Research Site

    A Coruña, 15006

  • Research Site

    Barakaldo, 48903

  • Research Site

    Barcelona, 08035

  • Research Site

    Barcelona, 08036

  • Research Site

    Bilbao (Vizcaya), 48013

  • Research Site

    L'Hospitalet de Llobregat, 08907

  • Research Site

    Las Palmas de Gran Canaria, 35020

  • Research Site

    Madrid, 28034

  • Research Site

    Madrid, 28040

  • Research Site

    Madrid, 28041

  • Research Site

    Oviedo, 33011

  • Research Site

    Santander, 39008

  • Research Site

    Seville, 41010

  • Research Site

    Seville, 41013

  • Research Site

    Valencia, 46026

  • Research Site

    Zaragoza, 50009

Other trials in Spain

Brazil13 sites
  • Research Site

    Belém, 66095-055

  • Research Site

    Belo Horizonte, 30150-221

  • Research Site

    Campinas, 13083

  • Research Site

    Juiz de Fora, 36010-570

  • Research Site

    Natal, 59025-050

  • Research Site

    Porto Alegre, 90035-000

  • Research Site

    Porto Alegre, 90480-000

  • Research Site

    Salvador, 40150-150

  • Research Site

    São José do Rio Preto, 15090-000

  • Research Site

    São Paulo, 01308-050

  • Research Site

    São Paulo, 05403-010

  • Research Site

    Serra, 29160-750

  • Research Site

    Vitória, 29050-400

Other trials in Brazil

Japan10 sites
  • Research Site

    Bunkyō City, 113-8655

  • Research Site

    Hiroshima, 734-8551

  • Research Site

    Iruma-Gun, 350-0495

  • Research Site

    Nagoya, 467-8602

  • Research Site

    Narita-shi, 286-8520

  • Research Site

    Okayama, 700-8558

  • Research Site

    Osaka, 565-0871

  • Research Site

    Sapporo, 060-8648

  • Research Site

    Sendai, 980-8574

  • Research Site

    Urayasu-shi, 279-0021

Other trials in Japan

France7 sites
  • Research Site

    Lille, 59037

  • Research Site

    Lyon, 69437

  • Research Site

    Nantes, 44093

  • Research Site

    Paris, 75010

  • Research Site

    Paris, 75651

  • Research Site

    Strasbourg, 67098

  • Research Site

    Toulouse, 31059

Other trials in France

Germany7 sites
  • Research Site

    Düsseldorf, 40225

  • Research Site

    Erlangen, 91054

  • Research Site

    Essen, 45147

  • Research Site

    Freiburg im Breisgau, 79106

  • Research Site

    Göttingen, 37075

  • Research Site

    Halle, 06120

  • Research Site

    Jena, 07747

Other trials in Germany

South Korea6 sites
  • Research Site

    Daejeon, 35015

  • Research Site

    Junggu, 22332

  • Research Site

    Seoul, 02447

  • Research Site

    Seoul, 03080

  • Research Site

    Seoul, 04763

  • Research Site

    Seoul, 6591

Other trials in South Korea

United Kingdom5 sites
  • Research Site

    Edinburgh, EH4 2XU

  • Research Site

    Liverpool, L9 7AL

  • Research Site

    London, SE5 9RS

  • Research Site

    Salford, M6 8HD

  • Research Site

    West Bromwich, B71 4HJ

Other trials in United Kingdom

Taiwan3 sites
  • Research Site

    Kaohsiung City, 83301

  • Research Site

    Taichung, 40705

  • Research Site

    Taoyuan City, 33305

Other trials in Taiwan

Australia2 sites
  • Research Site

    Camperdown, 2050

  • Research Site

    Murdoch, WA6150

Other trials in Australia

Turkey (Türkiye)2 sites
  • Research Site

    Altındağ-Ankara, 06230

  • Research Site

    Istanbul, 34093

Other trials in Turkey (Türkiye)

Poland1 site
  • Research Site

    Warsaw, 02-637

Other trials in Poland

About this study

Official title: A Phase 2/3, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ravulizumab in Adult Participants With Dermatomyositis

This is a Phase 2/3, double-blind, randomized, placebo-controlled, parallel group, multicenter study to evaluate the efficacy, safety, pharmacokinetics, pharmacodynamics, and immunogenicity of ravulizumab in adult participants with dermatomyositis (DM).

Read the detailed description

The study will be conducted in 2 parts: Part A (Phase 2) and Part B (Phase 3). There will be 3 periods in both Part A and Part B of this study: Screening Period, Randomized Controlled Period, and Open-Label Extension Period.

Conditions
Dermatomyositis
Being tested
Ravulizumab, Placebo
Keywords
Ravulizumab, ALXN1210, Ultomiris, Pharmacokinetics, Pharmacodynamics, Efficacy, DM
Medical subject headings
Dermatomyositis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RavulizumabDrug

    Also called ALXN1210, Ultomiris

    Intravenous dosing will consist of a loading dose followed by maintenance doses administered every 8 weeks (q8w). The maintenance dosing will be initiated 2 weeks after the loading dose is administered.

  • PlaceboDrug

    Intravenous dosing will consist of a loading dose followed by maintenance doses administered q8w. The maintenance dosing will be initiated 2 weeks after the loading dose is administered.

Study groups in NCT04999020
Study groupRoleWhat they receive
RavulizumabExperimentalParticipants will receive ravulizumab in both Parts A and B.
Receives: Drug: Ravulizumab
PlaceboPlacebo comparatorParticipants will receive placebo in both Parts A and B.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With International Myositis Assessment and Clinical Studies Total Improvement Score (IMACS-TIS) (TIS40) Response at Week 26 of the Randomized Controlled Period

    Data are presented for the number of participants with a TIS40 response, defined as an IMACS-TIS score ≥ 40 at Week 26. IMACS-TIS is a clinical instrument that encompasses 6 core set measure (CSMs) (physician, patient, extra-muscular global activity, muscle strength, Health Assessment Questionnaire [HAQ], and muscle enzyme levels). A Total Improvement Score (TIS: 0-100), was determined by summing scores in each CSM, and was based on the improvement and relative weight of each CSM. A higher score indicated greater improvement. TIS40 was considered a moderate improvement score.

    Measured: Week 26

Secondary outcomes (15)
  1. TIS at Week 26

    TIS scores ranged from 0-100 with higher scores indicating a greater improvement. Scores were determined by summing scores in each of the 6 CSMs of the IMAC (physician, patient, extra-muscular global activity, muscle strength, HAQ, and muscle enzyme levels). Clinically meaningful thresholds for improvement were defined as ≥ 20 point improvement response on IMACS-TIS (TIS20; mild), ≥ 40 point improvement response on IMACS TIS (TIS40; moderate) and ≥ 60 point improvement response on IMACS-TIS (TIS60; severe). Scores were based on the improvement and relative weight of each CSM. Data are presented for TIS (least squares mean) at Week 26.

    Measured: Week 26

  2. Change From Baseline In Cutaneous Dermatomyositis Disease Area And Severity Index (CDASI) Activity Score at Week 26

    The CDASI is an instrument that separately measures activity and damage in the skin of dermatomyositis (DM) participants. It contains 3 activity measures (erythema, scale, and erosion/ulceration) and 2 damage measures (poikiloderma and calcinosis). CDASI score is calculated by rating the severity of skin disease in 15 anatomical locations on the body based on the activity and damage components. CDASI was completed by the Clinician or Clinician-Investigator while examining the participant. Total CDASI scores ranged from 0-100, with higher scores indicating a greater disease severity. Change from baseline in CDASI Total Activity Score at Week 26 was analyzed using a mixed model repeated measures (MMRM). The MMRM model included the observed Total Activity Score values at post baseline visits (Week 26) as the dependent variable.

    Measured: Baseline, Week 26

  3. Number of Participants With Response Related to Muscle Enzymes: Normalization of Most Abnormal Baseline Enzyme at Week 26

    Laboratory tests were conducted to measure serum activities of muscle associated enzymes including creatine kinase (CK), alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), and aldolase. Data are presented for the number of participants who had an abnormal muscle enzyme at baseline that had been normalized at Week 26.

    Measured: Baseline, Week 26

  4. Change From Baseline In IMACS CSMs: Extra-Muscular Disease Activity Based on Myositis Disease Activity Assessment Tool (MDAAT) at Week 26

    The MDAAT assesses disease activity of extra-muscular organ systems and muscles in participants with DM. The validated MDAAT tool measures the degree of disease activity of extra-muscular organ systems and muscle on a 0-10 centimeter (cm) visual analog scale (VAS). Extra-muscular activity ranged between 0 and 10, where, 0 cm = absent and 10 cm = maximum disease activity.

    Measured: Baseline, Week 26

  5. Change From Baseline In IMACS CSMs: Physician Global Activity Assessment at Week 26

    The physician global activity assessment provides an overall rating of disease activity related to myositis. Disease activity is judged by the physician based on all information available at the time of evaluation, including the participant's appearance, medical history, physical examination, laboratory testing, and prescribed medical therapy. The global disease activity score is recorded on a 10-cm VAS, where 0 cm= no evidence of disease activity and 10 cm= extremely severe disease activity.

    Measured: Baseline, Week 26

  6. Change From Baseline In IMACS CSMs: Patient Global Activity Assessment at Week 26

    The patient global activity assessment provides an overall rating of disease activity related to myositis from the participant's perspective. Participants were asked to consider all of the active inflammation in their own muscles, skin, joints, intestines, heart, lungs, or other parts of the body that can improve with treatment. The patient global disease activity score was recorded on a 10-cm VAS that contained a smiley face at the 0-cm anchor and a sad face at the 10 cm anchor to help participants understand the scale. Scores ranged from 0 (no evidence of disease activity) to 10 (extremely active or severe disease activity).

    Measured: Baseline, Week 26

  7. Change From Baseline In IMACS CSMs: Manual Muscle Testing Subset 8 Muscles (MMT-8) at Week 26

    The purpose of the MMT-8 was to measure muscle strength as part of the physical examination. It included a subset of 8 muscle groups: neck flexors, deltoids, biceps, wrist, extensors, gluteus maximus and medius, quadriceps, and ankle dorsiflexors. Total MMT8 scores ranged from 0 (lowest strength) to 150 (highest strength).

    Measured: Baseline, Week 26

  8. Change From Baseline In IMACS CSMs: Health Assessment Questionnaire (HAQ) at Week 26

    The HAQ is a brief self-report questionnaire that assesses physical function pertaining to activities of daily living in a variety of domains. The HAQ includes 20 questions relating to 8 domains of function: dressing and grooming, arising, eating, walking, hygiene, reach, grip and usual activities. For each of the categories, participants reported the amount of difficulty they had in performing 2 or 3 specific subcategory items. The standard disability score is calculated from the 8 categories by dividing the sum of the individual categories by the number of categories answered, yielding a score from 0 (without any difficulty) to 3 (unable to do), with higher values indicating higher disability.

    Measured: Baseline, Week 26

  9. Number of Participants With CDASI Response (>=7-point Improvement) at Week 26

    The CDASI is an instrument that separately measures activity and damage in the skin of dermatomyositis (DM) participants. It contains 3 activity measures (erythema, scale, and erosion/ulceration) and 2 damage measures (poikiloderma and calcinosis). CDASI score is calculated by rating the severity of skin disease in 15 anatomical locations on the body based on the activity and damage components. CDASI was completed by the Clinician or Clinician-Investigator while examining the participant. Total CDASI scores ranged from 0-100, with higher scores indicating a greater disease severity.

    Data are presented for the number of participants with a CDASI response. Response was defined as a >=7 point improvement in participants who did not have an intercurrent event at or prior to the relevant timepoint.

    Measured: Week 26

  10. Number of Participants With Cutaneous Dermatomyositis Activity Physician's Global Assessment (CDA-IGA) Response at Week 26

    CDA-IGA is a scale that was created to measure disease severity in participants with skin disease. It is a 5-point scale (0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe) with morphologic descriptors for each score. The CDA-IGA was completed by the Investigator and was used to describe the overall appearance of lesions at a given time point. Data are presented for the number of participants with a CDA-IGA response at Week 26. A response was defined as participants with clear or almost clear skin (score of 0 or 1) who did not have an intercurrent event at or before the relevant timepoint.

    Measured: Week 26

  11. Number of Participants With ≥ 20-Point Improvement Response on IMACS-TIS (TIS20) Response at Week 26

    TIS20 was defined as a ≥20-point improvement response on IMACS-TIS. IMACS-TIS is a clinical instrument that encompasses 6 CSMs (physician, patient, extra-muscular global activity, muscle strength, HAQ, and muscle enzyme levels). A Total Improvement Score (TIS: 0-100), was determined by summing scores in each CSM, and was based on the improvement and relative weight of each CSM. Higher scores indicated greater improvement/response. TIS20 is considered a mild improvement score.

    Measured: Week 26

  12. Number of Participants With ≥ 60-Point Improvement Response on IMACS-TIS (TIS60) Response at Week 26

    TIS60 was defined as a ≥60-point improvement response on IMACS-TIS. IMACS-TIS is a clinical instrument that encompasses 6 CSMs (physician, patient, extra-muscular global activity, muscle strength, HAQ, and muscle enzyme levels). A Total Improvement Score (TIS: 0-100), was determined by summing scores in each CSM, and was based on the improvement and relative weight of each CSM. Higher scores indicated greater improvement/response. TIS60 is considered a severe improvement score.

    Measured: Week 26

  13. Time to First Response of TIS20, TIS40, or TIS60

    TIS20, 40 and 60 were defined as a ≥20, ≥40 and ≥60-point improvement response on IMACS-TIS respectively. IMACS-TIS is a clinical instrument that encompasses 6 CSMs (physician, patient, and extra-muscular global activity, muscle strength, HAQ, and muscle enzyme levels). A Total Improvement Score (TIS: 0-100), was determined by summing scores in each CSM, and was based on the improvement and relative weight of each CSM. Higher scores indicated greater improvement/response. TIS20, 40 and 60 were considered mild, moderate and severe improvement scores respectively. Data are presented for the time to first response of TIS20, TIS40, or TIS60. The median time to TIS20, TIS40, and TIS60 was defined at the time in which 50% of the participants experienced TIS20, TIS40, or TIS60, respectively, based on a Kaplan-Meier analysis.

    Measured: Baseline through Week 26

  14. Number of Participants With Clinical Worsening (CW) During the RCP At 2 Consecutive Visits

    CW was defined as one of the following:

    1. Physician's global activity VAS worsening ≥ 2 cm and MMT-8 worsening ≥ 20% compared to baseline
    2. Global extra muscular activity worsening ≥ 2 cm on the MDAAT VAS compared to baseline
    3. Any 3 of 5 CSMs (excluding muscle enzymes) worsening by ≥ 30% compared to baseline

    Data are presented for the number of participants with clinical worsening during the RCP at 2 consecutive visits.

    Measured: Baseline through Week 26

  15. Number of Participants Who Received Acute Rescue Therapy With Standard DM Treatment

    Acute rescue therapy with standard DM treatment included an increased dose of a medication that was being taken for DM or the initiation of a new DM treatment (glucocorticoid and/or immunosuppressive/immunomodulatory therapy [ISTs]). Data are presented for the number of participants who received acute rescue therapy with standard DM treatment.

    Measured: Baseline through Week 26

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Aug 2021
  2. Study start19 Nov 2021
  3. Primary completion26 Oct 2023
  4. Study completion8 May 2024

Why it stopped: Sponsor decision

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
38 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04999020
Sponsor's protocol ID
ALXN1210-DM-310
Other IDs
2021-001200-15
Status last verified
Jul 2025
First submitted
4 Aug 2021
Last updated
9 Jul 2025
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Alexion has a public commitment to allow requests for access to study data and will be supplying a protocol, CSR, and plain language summaries.

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing Ravulizumab in people with Dermatomyositis, run by Alexion Pharmaceuticals, Inc. at 111 sites in 13 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 9 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 111 sites in United States, Italy, Spain, Brazil, Japan and 8 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 6 Dec 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With International Myositis Assessment and Clinical Studies Total Improvement Score (IMACS-TIS) (TIS40) Response at Week 26 of the Randomized Controlled Period (time frame: Week 26). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jul 2025.

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