AzTrials
AzTrials

Active Systemic Lupus ErythematosusPhase 2NCT04680637

Efficacy and Safety of Efavaleukin Alfa in Subjects With Active Systemic Lupus Erythematosus

A Phase 2 study testing Efavaleukin Alfa in people with Active Systemic Lupus Erythematosus, run by Amgen at 150 sites in 19 countries.

Terminated

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

Official record
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Trial summary

The primary objective is to evaluate the efficacy and safety of efavaleukin alfa in subjects with active systemic lupus erythematosus. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Active Systemic Lupus Erythematosus
What is being tested?
Efavaleukin Alfa
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
168 participants
Where
150 sitesin 19 countries
Study dates
6 May 2021to 22 May 2023
Phase
Phase 2
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 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participant has provided informed consent prior to initiation of any study specific activities/procedures.
  • Participant is aged between 18 and 75.
  • Fulfills classification criteria for systemic lupus erythematosus (SLE) according to the 2019 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria for SLE with antinuclear antibody ≥ 1:80 by immunofluorescence on Hep-2 cells being present at screening.
  • Hybrid SLEDAI score ≥ 6 points with a "Clinical" hSLEDAI score ≥ 4 points. The "Clinical" hSLEDAI is the hSLEDAI assessment score without the inclusion of points attributable to laboratory results, including urine or immunologic parameters.
  • British-Isles Lupus Assessment Group (BILAG) index score (BILAG 2004) of ≥ 1 A item or ≥ 2 B items.
  • Must be taking ≥ 1 of the following SLE treatments (or regional equivalent): hydroxychloroquine, chloroquine, quinacrine, mycophenolate mofetil, azathioprine, methotrexate, dapsone, or oral calcineurin inhibitors, or OCS. A participant may enter the study on OCS alone (prednisone ≥ 10 mg/day or equivalent) only if the participant has previously documented trial of anti-malarial or immunosuppressant treatment for SLE. Participants must be on a stable dose for ≥ 8 weeks prior to screening for all antimalarials and immunosuppressants, with the exception of OCS doses which must be stable for ≥ 2 weeks prior to screening.
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  • For participants taking OCS, dose must be ≤ 20 mg/day of prednisone or OCS equivalent, and the dose must be stable at baseline visit and for ≥ 2 weeks prior to screening visit.
  • Stability of SLE treatments: OCS and other immunosuppressants/immunomodulator agents and doses must be stable since screening visit.
  • Disease activity: active disease as indicated by clinical hSLEDAI score ≥ 4 must be observed (clinical hSLEDAI score is the hSLEDAI assessment score without the inclusion of points attributable to laboratory results including urine and immunologic parameters).

Who cannot join

  • Lupus nephritis if any of the following are present: urine protein creatinine ratio ≥ 2000 mg/g (or equivalent) at screening, OR requiring induction therapy currently or within 1 year prior to screening, OR histological evidence (if available) of diffuse proliferative glomerulonephritis within 12 weeks prior to screening.
  • Active CNS lupus within 1 year prior to screening including, but not limited to, aseptic meningitis, ataxia, CNS vasculitis, cranial neuropathy, demyelinating syndrome, optic neuritis, psychosis, seizures, or transverse myelitis.
  • Currently present or within 1 year prior to screening a diagnosis of any chronic inflammatory disease other than SLE (eg, rheumatoid arthritis) which would interfere with SLE disease assessment.
  • History of any disease other than SLE that has required treatment with oral or parenteral corticosteroids for > 2 weeks within 4 months prior to screening.
  • Active infection (including chronic or localized infections) for which anti-infectives are indicated currently or within 4 weeks prior to screening visit OR presence of serious infection, defined as requiring hospitalization or intravenous anti-infectives within 8 weeks prior to screening visit.
  • Active tuberculosis or latent tuberculosis with no documented past history of adequate treatment per local standard of care.
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  • Positive test for tuberculosis during creening defined as: either a positive or indeterminate QuantiFERON®-TB or T-spot test OR positive purified protein derivative (PPD) (≥5 mm of induration at 48 to 72 hours after test is placed).
  • Positive for hepatitis B surface antigen (HBsAg); or positive for hepatitis B core antibody (HBcAb). A history of hepatitis B vaccination without history of hepatitis B infection (ie, positive hepatitis B surface antibody (HBsAb), negative HBsAg and negative HBcAb) is allowed.
  • Positive for hepatitis C antibody.
  • Known history of HIV or positive HIV test at screening.
  • Presence of 1 or more significant concurrent medical conditions, including but not limited to the following:
  • poorly controlled diabetes (hemoglobin A1C > 7) or hypertension
  • symptomatic heart failure (New York Heart Association class III or IV)
  • myocardial infarction or unstable angina pectoris within the past 12 months prior to screening
  • severe chronic pulmonary disease requiring oxygen therapy
  • multiple sclerosis or any other demyelinating disease
  • Any history of malignancy with the following exceptions:
  • resolved non-melanoma skin cancers > 5 years prior to screening
  • resolved cervical carcinoma > 5 years prior to screening
  • resolved breast ductal carcinoma in situ > 5 years of screening
  • Currently receiving or had treatment with: cyclophosphamide, chlorambucil, nitrogen mustard, or any other alkylating agent within 6 months prior to screening or sirolimus within 4 weeks prior screening.
  • Currently receiving or had treatment with a Janus kinase (JAK) inhibitor within 3 months or less than 5 drug half-lives (whichever is longer) prior to screening.
  • Currently receiving or had treatment with an immune checkpoint inhibitor (eg, programmed death 1 [PD-1] inhibitor, programmed death ligand 1 [PD-L1] inhibitor, cytotoxic T-lymphocyte associated protein 4 [CTLA-4] inhibitor).
  • Note: Abatacept is not considered a CTLA-4 inhibitor and is referred to below.
  • Currently receiving or had treatment within 12 months prior to screening with T-cell depleting agents (eg, antithymocyte globulin, Campath).
  • Currently receiving of had treatment with an interleukin 2 (IL-2) based therapy (eg, Proleukin).
  • Current or previous treatment with a biologic agent with immunosuppressive/immunomodulatory activity as follows: rituximab within 6 months prior to screening; abatacept and belimumab within the past 3 months prior to screening; other biologics within < 5 drug half lives prior to screening.
  • Participants who have received intraarticular, intralesional, or intramuscular corticosteroids within 2 weeks prior to screening or intravenous corticosteroids within 6 weeks prior to screening.
  • Participants who have received live vaccines within 5 weeks prior to screening, or plan to receive live vaccines during the treatment period and up to 6 weeks after the end of treatment period in the study.
  • Currently receiving treatment in another investigational device or drug study.
  • Ending a treatment with an investigational drug or investigational device less than 3 months or 5 half-lives from the last dose of the investigational drug (whichever is longer) at screening.

Trial locations and contacts

150 sites in 19 countries.

150 sites in 19 countries

United States51 sites
  • Arthritis and Rheumatology Institute

    Allen, Texas, 75013

  • Arthritis and Rheumatic Disease Specialties

    Aventura, Florida, 33180

  • Life Clinical Trials

    Aventura, Florida, 33180

  • University of Alabama at Birmingham,Arthritis Clinical Intervention Program

    Birmingham, Alabama, 35294

  • New York University Langone Ambulatory Care Brooklyn Heights

    Brooklyn, New York, 11201

  • University of North Carolina at Chapel Hill Thurston Arthritis Research Center

    Chapel Hill, North Carolina, 27599

  • Joint and Muscle Research Institute

    Charlotte, North Carolina, 28204

  • DJL Clinical Research PLLC

    Charlotte, North Carolina, 28210

  • Javara

    Charlotte, North Carolina, 28210

  • Atrium Health Rheumatology

    Charlotte, North Carolina, 28211

  • University of Chicago

    Chicago, Illinois, 60637

  • Precision Comprehensive Clinical Research Solutions

    Colleyville, Texas, 76034

  • Columbia Arthritis Center, PA

    Columbia, South Carolina, 29204

  • Texas Arthritis Center PA

    El Paso, Texas, 79902

  • Centre for Rheumatology Immunology and Arthritis

    Fort Lauderdale, Florida, 33309

  • Arizona Arthritis and Rheumatology Associates PC

    Gilbert, Arizona, 85297

  • Arizona Arthritis And Rheumatology Associates PC

    Glendale, Arizona, 85306

  • Michigan Rheumatology Group, PC - Grand Blanc Office

    Grand Blanc, Michigan, 48439

  • Piedmont Arthritis Clinic

    Greenville, South Carolina, 29601

  • GNP Research

    Hollywood, Florida, 33024

  • Western Kentucky Rheumatology PLLC

    Hopkinsville, Kentucky, 42240

  • Biopharma Informatic, LLC

    Houston, Texas, 77043

  • Accurate Clinical Management

    Houston, Texas, 77084

  • Laila A Hassan, MD, PA

    Houston, Texas, 77089

  • West Tennessee Research Institute, LLC

    Jackson, Tennessee, 38305

  • University of Tennessee Medical Center

    Knoxville, Tennessee, 37920

  • Accurate Clinical Research

    Lake Charles, Louisiana, 70605

  • Arthritis and Rheumatology of Michigan

    Lansing, Michigan, 48910

  • Loma Linda University Health Care

    Loma Linda, California, 92354

  • University of California Los Angeles

    Los Angeles, California, 90024

  • Feinstein Institute for Medical Research

    Manhasset, New York, 11030

  • Ramesh C Gupta MD

    Memphis, Tennessee, 38119

  • Icahn School of Medicine at Mount Sinai

    New York, New York, 10029

  • Arthritis and Rheumatology Center of Oklahoma PLLC

    Oklahoma City, Oklahoma, 73102

  • Oklahoma Medical Research Foundation

    Oklahoma City, Oklahoma, 73104

  • University of California Irvine

    Orange, California, 92868

  • Millennium Research

    Ormond Beach, Florida, 32174

  • University of Pittsburgh Medical Center Lupus Center of Excellence

    Pittsburgh, Pennsylvania, 15213

  • Trinity Universal Research Associates, LLC

    Plano, Texas, 75024

  • Integral Rheumatology and Immunology Specialists

    Plantation, Florida, 33324

  • Clinical Trials of Texas

    San Antonio, Texas, 78229

  • University of Texas Health Science Center at San Antonio Medical Arts Research Clinic Marc

    San Antonio, Texas, 78229

  • Greater Chicago Specialty Physicians

    Schaumburg, Illinois, 60195

  • Clinic of Robert Hozman, MD - Clinical Investigational Specialists, Inc

    Skokie, Illinois, 60076

  • Suncoast Medical Clinic

    St. Petersburg, Florida, 33710

  • State University of New York - Upstate Medical University

    Syracuse, New York, 13210

  • Baycare Medical Group Inc

    Tampa, Florida, 33614

  • Institute for Clinical and Translation Research at Einstein and Montefiore Clinical Research Center

    The Bronx, New York, 10461

  • Arizona Arthritis and Rheumatology Associates PC

    Tucson, Arizona, 85704

  • Robin K Dore MD Inc

    Tustin, California, 92780

  • Arthritis and Osteoporosis Clinic

    Waco, Texas, 76710

Other trials in United States

Japan19 sites
  • Juntendo University Hospital

    Bunkyo-ku, Tokyo, 113-8431

  • National Hospital Organization Chibahigashi National Hospital

    Chiba, Chiba, 260-8712

  • St Lukes International Hospital

    Chuo-ku, Tokyo, 104-8560

  • Seirei Hamamatsu General Hospital

    Hamamatsu, Shizuoka, 430-8558

  • Hiroshima University Hospital

    Hiroshima, Hiroshima, 734-8551

  • Eiraku Clinic

    Kagoshima, Kagoshima-ken, 890-0063

  • Kagoshima University Hospital

    Kagoshima, Kagoshima-ken, 890-8520

  • Kanazawa University Hospital

    Kanazawa, Ishikawa-ken, 920-8641

  • St Marianna University Hospital

    Kawasaki-shi, Kanagawa, 216-8511

  • Hospital of the University of Occupational and Environmental Health Japan

    Kitakyushu-shi, Fukuoka, 807-8556

  • National Hospital Organization Tokyo Medical Center

    Meguro-ku, Tokyo, 152-8902

  • Nagasaki University Hospital

    Nagasaki, Nagasaki, 852-8501

  • Japan Community Healthcare Organization Chukyo Hospital

    Nagoya, Aichi-ken, 457-8510

  • Nagoya City University Hospital

    Nagoya, Aichi-ken, 467-8602

  • Sapporo City General Hospital

    Sapporo, Hokkaido, 060-8604

  • Hokkaido University Hospital

    Sapporo, Hokkaido, 060-8648

  • National University Corporation Tohoku University Tohoku University Hospital

    Sendai, Miyagi, 980-8574

  • Keio University Hospital

    Shinjuku-ku, Tokyo, 160-8582

  • Center Hospital of the National Center for Global Health and Medicine

    Shinjuku-ku, Tokyo, 162-8655

Other trials in Japan

Chile8 sites
  • Corporacion de Beneficiencia Osorno

    Osorno, 5311092

  • Investigacion y Terapias Reumatologicas Innovadoras LTDA - Interin LTDA

    Providencia, Santiago Metropolitan, 7500010

  • Enroll SpA

    Providencia, Santiago Metropolitan, 7500587

  • Sociedad de prestaciones Medicas y Paramedicas Goecke Gatica y Compania Limitada - Prosalud

    Providencia, Santiago Metropolitan, 7510047

  • Estudios Clinicos Limitada - Centro de Estudios Reumatologicos

    Santiago, 7501126

  • CECIM

    Santiago, 8320000

  • Sociedad de Prestaciones Medicas Intermedica Limitada

    Valdivia, 5111847

  • Oncocentro Apys

    Viña del Mar, 2520598

Other trials in Chile

Italy8 sites
  • Azienda Ospedaliera Universitaria Careggi

    Florence, 50139

  • Università degli studi della Campania Luigi Vanvitelli

    Naples, 80131

  • Azienda Ospedaliera di Padova

    Padova, 35128

  • Azienda Ospedaliera Policlinico Umberto I

    Roma, 00161

  • Policlinico Universitario Agostino Gemelli

    Roma, 00168

  • Azienda Ospedaliera Ordine Mauriziano di Torino

    Torino, 10128

  • Azienda Ospedaliero Universitaria Integrata Santa Maria della Misericordia

    Udine, 33100

  • Centro Ricerche Cliniche

    Verona, 37134

Other trials in Italy

Spain8 sites
  • Hospital de la Santa Creu i Sant Pau

    Barcelona, Catalonia, 08041

  • Hospital Universitario Reina Sofia

    Córdoba, Andalusia, 14004

  • Corporacio Sanitaria Parc Tauli

    Sabadell, Catalonia, 08208

  • Hospital Universitario Hospiten Rambla

    Santa Cruz de Tenerife, Canary Islands, 38001

  • Hospital Clinico Universitario de Santiago

    Santiago de Compostela, Galicia, 15706

  • Hospital Infanta Luisa

    Seville, Andalusia, 41010

  • Hospital Universitari i Politecnic La Fe

    Valencia, Valencia, 46026

  • Hospital Universitario Araba

    Vitoria-Gasteiz, Basque Country, 01009

Other trials in Spain

Greece7 sites
  • Athens Naval Hospital

    Athens, 11521

  • Laiko General Hospital

    Athens, 11527

  • Attiko Hospital

    Athens, 12462

  • University Hospital of Heraklion

    Heraklion, 71500

  • Olympion Hospital-General Clinic of Patras AE

    Pátrai, 26443

  • Euromedica - Kyanous Stavros

    Thessaloniki, 54636

  • Ippokrateio Hospital of Thessaloniki

    Thessaloniki, 54642

Other trials in Greece

Colombia6 sites
  • Centro Integral de Reumatología del Caribe Circaribe SAS

    Barranquilla, Atlántico, 080002

  • Centro de Investigacion en Reumatologia y Especialidades Medicas SAS

    Bogota, Cundinamarca, 110221

  • Solano y Terront Servicios Medicos Ltda - Uniendo

    Bogota, Cundinamarca, 110221

  • Centro Medico Julian Coronel

    Cali, Valle del Cauca Department, 760035

  • Mediservis del Tolima IPS SAS

    Ibague, Tolima Department, 730006

  • Hospital Pablo Tobon Uribe

    Medellín, Antioquia, 050034

Other trials in Colombia

Mexico6 sites
  • Centro de Investigacion Integral Medivest SC

    Chihuahua City, 31203

  • Phylasis Clínicas Research S. De R. L. De C. V.

    Cuautitlán Izcalli, 54769

  • Centro Integral en Reumatologia SA de CV

    Guadalajara, Jalisco, 44160

  • Centro de Estudios de Investigacion Basica y Clinica, Sc

    Guadalajara, Jalisco, 44690

  • CITER SA de CV (Centro de Investigación y Tratamiento de las Enfermedades Reumáticas SA de CV)

    Mexico City, Mexico City, 06700

  • Eukarya Pharmasite sc

    Monterrey, Nuevo León, 64718

Other trials in Mexico

Poland6 sites
  • Centrum medyczne intercore sp zoo

    Bydgoszcz, 85-605

  • Centrum Medyczne Pratia Czestochowa

    Częstochowa, 42-200

  • Centrum Badan Klinicznych Wojciech Brzezicki

    Malbork, 82-200

  • NZOZ Lecznica MAK-MED sc

    Nadarzyn, 05-830

  • Gabinety Lekarskie RIVERMED

    Poznan, 61-441

  • Reumatop Grzegorz Rozumek, Karin Pistorius

    Wroclaw, 52-210

Other trials in Poland

Russia6 sites
  • Limited liability company Scientific Research Medical Complex Your Health

    Kazan', 420097

  • FSBSI SRI of Rheumatology na V A Nasonova

    Moscow, 115522

  • I M Sechenov First Medical University of the MoH of RF

    Moscow, 119435

  • Saint-Petersburg State Budget Healthcare Institution Clinical Rheumatology Hospital 25

    Saint Petersburg, 190068

  • LLC Medical Sanitary Unit №157

    Saint Petersburg, 196066

  • Center for medical consultations and research - practice

    Yaroslavl, 150003

Other trials in Russia

Bulgaria4 sites
  • Diagnostic-Consultative Center Sveti Georgi EOOD

    Plovdiv, 40002

  • Medical Center Excelsior OOD

    Sofia, 1407

  • Medical Center Academy EOOD

    Sofia, 1612

  • University Multiprofile Hospital for Active Treatment Sveti Ivan Rilski EAD

    Sofia, 1612

Other trials in Bulgaria

France4 sites
  • Centre Hospitalier Universitaire de Montpellier Hopital Lapeyronie

    Montpellier, 34295

  • Centre Hospitalier Universitaire de Strasbourg - Nouvel Hopital Civil

    Strasbourg, 67091

  • Centre Hospitalier Universitaire de Toulouse - Hopital Rangueil

    Toulouse, 31059

  • Centre Hospitalier Universitaire de Nancy - Hopital de Brabois

    Vandœuvre-lès-Nancy, 54511

Other trials in France

South Korea4 sites
  • Daegu Catholic Universtiy Medcial Center

    Daegu, 42472

  • Seoul National University Hospital

    Seoul, 03080

  • Hanyang University Seoul Hospital

    Seoul, 04763

  • Ajou University Hospital

    Suwon-si, Gyeonggi-do, 16499

Other trials in South Korea

Taiwan4 sites
  • Kaohsiung Chang Gung Memorial Hospital

    Kaohsiung City, 83301

  • Chung Shan Medical University Hospital

    Taichung, 40201

  • Taichung Veterans General Hospital

    Taichung, 40705

  • National Taiwan University Hospital

    Taipei, 10002

Other trials in Taiwan

Turkey (Türkiye)4 sites
  • Cukurova Universitesi Balcali Hastanesi Saglik Uygulama ve Arastirma Merkezi

    Adana, 01790

  • Hacettepe Universitesi Tip Fakultesi

    Ankara, 06100

  • Akdeniz Universitesi Tip Fakultesi

    Antalya, 07070

  • Istanbul Universitesi Istanbul Tip Fakultesi

    Istanbul, 34093

Other trials in Turkey (Türkiye)

Switzerland2 sites
  • Universitaetsspital Basel

    Basel, 4031

  • Kantonsspital St Gallen

    Sankt Gallen, 9007

Other trials in Switzerland

Austria1 site
  • Medizinische Universitaet Graz

    Graz, 8036

Other trials in Austria

Canada1 site
  • Toronto Western Hospital

    Toronto, Ontario, M5T 2S8

Other trials in Canada

Hong Kong1 site
  • Tuen Mun Hospital

    New Territories

Other trials in Hong Kong

About this study

Official title: A Phase 2b Dose Ranging Study to Evaluate the Efficacy and Safety of Efavaleukin Alfa in Subjects With Active Systemic Lupus Erythematosus With Inadequate Response to Standard of Care Therapy

The primary objective is to evaluate the efficacy and safety of efavaleukin alfa in subjects with active systemic lupus erythematosus.

Being tested
Efavaleukin Alfa, Placebo, Standard of Care

What participants receive

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

  • Efavaleukin AlfaDrug

    Also called AMG 592

    Administered as a subcutaneous (SC) injection.

  • PlaceboDrug

    Administered as a subcutaneous (SC) injection.

  • Standard of CareOther

    Standard of care procedures and therapies for managing active systemic lupus erythematosus will be carried out according to each investigator's standard procedures.

Study groups in NCT04680637
Study groupRoleWhat they receive
Placebo + Standard of CarePlacebo comparatorNot described
Receives: Drug: Placebo; Other: Standard of Care
Efavaleukin Alfa Dose Level One + Standard of CareExperimentalNot described
Receives: Drug: Efavaleukin Alfa; Other: Standard of Care
Efavaleukin Alfa Dose Level Two + Standard of CareExperimentalNot described
Receives: Drug: Efavaleukin Alfa; Other: Standard of Care
Efavaleukin Alfa Dose Level Three + Standard of CareExperimentalNot described
Receives: Drug: Efavaleukin Alfa; Other: Standard of Care

What is being measured

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

  1. Number of Participants Who Achieved a Systemic Lupus Erythematosus Responder Index 4 (SRI-4) Response at Week 52

    A participant achieved an SRI-4 response if all the following criteria were met:

    • ≥ 4-point reduction from baseline in Hybrid Systemic Lupus Erythematosus Disease Activity Index (hSLEDAI) score (scale 0-105, with higher scores indicating more disease activity).
    • No new British-Isles Lupus Assessment Group (BILAG) A score and no > 1 new BILAG B organ domain scores compared with baseline. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active), B (moderate activity), C (minor activity), D (stable) or E (never present).
    • < 0.3-points deterioration from baseline in Physician Global Assessment (PGA) visual analogue (VAS) score (scale 0 to 3, with higher scores indicating more severe disease).

    Participants were considered non-responders for using more than protocol-permitted therapies.

    Measured: Week 52

Secondary outcomes (30)
  1. Number of Participants Who Achieved a BILAG-based Composite Lupus Assessment (BICLA) Response at Week 52

    A participant achieved a BICLA response if all the following criteria were met:

    • At least 1 gradation of improvement in baseline BILAG domain scores in all body systems with moderate or severe disease activity at entry and no > 1 BILAG B domain scores compared with baseline. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active), B (moderate activity), C (minor activity), D (stable) or E (never present).
    • No worsening of the hSLEDAI score from baseline (scale 0-105, with higher scores indicating more disease activity).
    • < 0.3-points deterioration from baseline in PGA VAS (scale 0 to 3, with higher scores indicating more severe disease).
    • No initiation of non-protocol treatment.

    Measured: Week 52

  2. Number of Participants Who Achieved a Lupus Low Disease Activity State (LLDAS) Response at Week 52

    A participant achieved an LLDAS response if all the following criteria were met:

    • hSLEDAI ≤ 4 (scale 0-105, higher scores indicating more disease activity) with no activity in major organ systems (renal [proteinuria, hematuria, pyuria, urinary casts], central nervous system [seizure, psychosis, organic brain syndrome, cranial nerve disorder, cerebrovascular accident], cardiopulmonary [pericarditis, pleurisy], vasculitis and fever) \& no hemolytic anemia or gastrointestinal activity in BILAG. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active) to E (never present).
    • No new lupus disease activity compared with previous assessment defined as no new descriptor scores in hSLEDAI.
    • A score of < 1 in PGA VAS score (scale 0 to 3, with higher scores indicating more severe disease).
    • Current prednisolone dose ≤ 7.5 mg daily.
    • No increase or initiation of immunosuppressive drugs.

    Measured: Week 52

  3. Number of Participants With a Reduction of Oral Corticosteroids (OCS) to ≤ 7.5 mg/Day by Week 44 and Sustained Through Week 52 in Participants With a Baseline OCS Dose ≥ 10 mg/Day

    Participants taking OCS could begin tapering OCS after the Week 12 assessment up to the Week 44 assessment with initiation of tapering based upon clinical judgement of the treating physician. The tapering schedule was at the discretion of the investigator but should not have been tapered more than 20% of the prior dose per week. Tapering OCS before Week 12 was not encouraged but may have been allowed based upon investigator's judgement. Between weeks 44 and 52, the OCS dosing must again have remained stable.

    Measured: Baseline to Week 52

  4. Number of Participants Who Achieved a SRI-4 Response at Week 24

    A participant achieved an SRI-4 response if all the following criteria were met:

    • ≥ 4-point reduction from baseline in hSLEDAI score (scale 0-105, with higher scores indicating more disease activity).
    • No new BILAG A score and no > 1 new BILAG B organ domain scores compared with baseline. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active), B (moderate activity), C (minor activity), D (stable) or E (never present).
    • < 0.3-points deterioration from baseline in PGA VAS score (scale 0 to 3, with higher scores indicating more severe disease).

    Participants were considered non-responders for using more than protocol-permitted therapies.

    Measured: Week 24

  5. Number of Participants Who Achieved a BICLA Response at Week 24

    A participant achieved a BICLA response if all the following criteria were met:

    • At least 1 gradation of improvement in baseline BILAG domain scores in all body systems with moderate or severe disease activity at entry and no > 1 BILAG B domain scores compared with baseline. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active), B (moderate activity), C (minor activity), D (stable) or E (never present).
    • No worsening of the hSLEDAI score from baseline (scale 0-105, with higher scores indicating more disease activity).
    • < 0.3-points deterioration from baseline in PGA VAS (scale 0 to 3, with higher scores indicating more severe disease).
    • No initiation of non-protocol treatment.

    Measured: Week 24

  6. Number of Participants With a hSLEDAI Response at Week 24 and Week 52

    The hSLEDAI is a global index that evaluates disease activity and includes both laboratory and clinical parameters. The score ranges from 0 to 105, with higher scores indicating more disease activity.

    A participant achieved a hSLEDAI response if there was a ≥ 4-point reduction in hSLEDAI from baseline.

    Measured: Week 24 and Week 52

  7. Number of Participants With an Improvement From Baseline in Tender and Swollen Joint Count ≥ 50% at Weeks 8, 12, 24, 36, and 52 in Participants With ≥ 6 Tender and Swollen Joints in Hands and Wrists

    The swollen and tender join count assessments were performed at the site by an experienced independent and blinded joint evaluator.

    Joints in hands and wrists were scored for the simultaneous presence (1) or absence (0) of swelling and tenderness. Scores ranged from 0-28. A higher score indicates more severe disease.

    Measured: Weeks 8, 12, 24, 36 and 52

  8. Number of Participants With an Improvement From Baseline in Cutaneous Lupus Erythematosus Area and Severity Index (CLASI) Activity Score ≥ 50% at Week 8, 12, 24, 36, and 52 in Participants With a CLASI Activity Score ≥ 8 at Baseline

    The CLASI consists of 2 scores, the first summarizes the activity of the disease while the second is a measure of the damage done by the disease. Activity is scored based on erythema, scale/hyperkeratosis, mucous membrane involvement, acute hair loss and non-scarring alopecia. The total score ranges from 0-70, with higher scores indicating more severe disease.

    Measured: Weeks 8, 12, 24, 36 and 52

  9. Annualized Flare Rate Over 52 Weeks

    A flare was defined as a BILAG score designation of "worse" or "new" resulting in a B score in ≥ 2 organs or an A score in ≥ 1 organ. The BILAG index evaluates disease activity in 9 separate organ systems. Each of the organ systems are allocated an alphabetical score of A (most active), B (moderate activity), C (minor activity), D (stable) or E (never present).

    The annualized flare rate was calculated as the number of flares divided by the flare exposure time in days multiplied by 365.25.

    Measured: Up to 52 weeks

  10. Change From Baseline in Fatigue Standardized Score Using the Patient-Reported Outcome Measurement Information System (PROMIS) Fatigue Short Form (SF) 7a Instrument at Week 12, 24, 36 and 52

    The PROMIS Fatigue SF 7a assesses the experience of fatigue as well as its impact on physical, mental and social activities. The score ranges from 7 to 35, with higher scores indicating more fatigue. A negative change from baseline indicates a reduction in fatigue.

    Efficacy data collected after the study termination decision date were censored and excluded from analyses for that particular visit.

    Measured: Baseline to Week 12, 24, 36 and 52

  11. Change From Baseline in the Physical Component Score of the Medical Outcomes Short Form-36 Questionnaire Version 2 (SF-36V2) at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  12. Change From Baseline in the Mental Component Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  13. Change From Baseline in the Physical Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  14. Change From Baseline in the Social Role Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  15. Change From Baseline in the Physical Role Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  16. Change From Baseline in the Bodily Pain Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  17. Change From Baseline in the Mental Health Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  18. Change From Baseline in the Emotional Role Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  19. Change From Baseline in the Vitality Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  20. Change From Baseline in the General Health Domain Score of the SF-36V2 at Week 12, 24, 36 and 52

    The SF-36v2 contains 36 items and yields assessments of 8 domains of health-related quality of life:

    1. Limitations in physical activities because of health problems.
    2. Limitations in social activities because of physical or emotional problems.
    3. Limitations in usual role activities because of physical health problems.
    4. Bodily pain.
    5. General mental health (psychological distress and well-being).
    6. Limitations in usual role activities because of emotional problems.
    7. Vitality (energy and fatigue).
    8. General health perceptions.

    The scores from the 8 domains will be evaluated independently and aggregated into 2 norm-based summary component measures of physical and mental health. The recall period is the past 7 days. The score ranges from 0-100 for the summary components and for each domain, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  21. Change From Baseline in the Physical Health Domain Score of the Lupus Quality of Life (LupusQoL) at Week 12, 24, 36 and 52

    The LupusQoL is a systemic lupus erythematosus (SLE)-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  22. Change From Baseline in the Pain Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  23. Change From Baseline in the Planning Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  24. Change From Baseline in the Intimate Relationship Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  25. Change From Baseline in the Burden to Others Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  26. Change From Baseline in the Emotional Health Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  27. Change From Baseline in the Body Image Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  28. Change From Baseline in the Fatigue Domain Score of the LupusQoL at Week 12, 24, 36 and 52

    The LupusQoL is a SLE-specific health-related QoL instrument and consists of 8 domains:

    1. Physical health.
    2. Pain.
    3. Planning.
    4. Intimate relationships.
    5. Burden to others.
    6. Emotional health.
    7. Body image.
    8. Fatigue.

    The score for each domain ranges from 0-100, with higher scores indicating better outcomes. A positive change from baseline indicates an improvement in outcomes.

    Measured: Baseline to Week 12, 24, 36 and 52

  29. Number of Participants Who Experienced a Treatment-emergent Adverse Event (TEAE)

    A TEAE was defined as any untoward medical occurrence in a clinical study participant irrespective of a causal relationship with the study treatment and had emerged or worsened during treatment.

    A serious TEAE was defined as any untoward medical occurrence that, met at least 1 of the following criteria:

    • Resulted in death (fatal).
    • Was immediately life-threatening.
    • Required in-patient hospitalization or prolongation of existing hospitalization.
    • Resulted in persistent or significant disability/incapacity.
    • Was a congenital anomaly/birth defect.
    • Was any other medically important serious event.

    Clinically significant changes from baseline in laboratory values and vital signs were also recorded as TEAEs.

    Measured: Day 1 to Week 56

  30. Serum Efavaleukin Alfa Concentrations by Timepoint

    Serum efavaleukin alfa concentrations by timepoint after multiple dose subcutaneous administration of efavaleukin alfa to participants with active systemic lupus erythematosus. Lower limit of quantification= 0.100 ng/mL.

    Measured: Day 1: 6-24 and 48-96 hrs, Day 29, Day 43: 6-24 and 48-96 hrs, Day 85, Day 169, Day 253, Day 309, and Day 365

Timeline

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

  1. First posted23 Dec 2020
  2. Study start6 May 2021
  3. Primary completion22 May 2023
  4. Study completion22 May 2023

Why it stopped: The trial was terminated prematurely as it met pre-defined criteria for futility at IA3.

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
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
168 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04680637
Sponsor's protocol ID
20200234
Status last verified
Jun 2024
First submitted
18 Dec 2020
Last updated
28 Jun 2024
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request

Publications

  • Garces S, Karis E, Merrill JT, Askanase AD, Kalunian K, Mo M, Milmont CE. Improving resource utilisation in SLE drug development through innovative trial design. Lupus Sci Med. 2023 Jul;10(2):e000890. doi: 10.1136/lupus-2022-000890.

    PubMed 37491104

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Efavaleukin Alfa in people with Active Systemic Lupus Erythematosus, run by Amgen at 150 sites in 19 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 9 inclusion and 31 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 28 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 150 sites in United States, Japan, Chile, Italy, Spain and 14 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 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.

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 28 Jun 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 Who Achieved a Systemic Lupus Erythematosus Responder Index 4 (SRI-4) Response at Week 52 (time frame: Week 52). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04680637, which also lists 1 linked publication.

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 28 Jun 2024.

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