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.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Switzerland2 sites
Universitaetsspital Basel
Basel, 4031
Kantonsspital St Gallen
Sankt Gallen, 9007
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.
- Conditions
- 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 group | Role | What they receive |
|---|---|---|
| Placebo + Standard of Care | Placebo comparator | Not described Receives: Drug: Placebo; Other: Standard of Care |
| Efavaleukin Alfa Dose Level One + Standard of Care | Experimental | Not described Receives: Drug: Efavaleukin Alfa; Other: Standard of Care |
| Efavaleukin Alfa Dose Level Two + Standard of Care | Experimental | Not described Receives: Drug: Efavaleukin Alfa; Other: Standard of Care |
| Efavaleukin Alfa Dose Level Three + Standard of Care | Experimental | Not 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.
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)
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
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
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
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
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
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
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
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
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
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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Limitations in physical activities because of health problems.
- Limitations in social activities because of physical or emotional problems.
- Limitations in usual role activities because of physical health problems.
- Bodily pain.
- General mental health (psychological distress and well-being).
- Limitations in usual role activities because of emotional problems.
- Vitality (energy and fatigue).
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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:
- Physical health.
- Pain.
- Planning.
- Intimate relationships.
- Burden to others.
- Emotional health.
- Body image.
- 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
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
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.
- First posted23 Dec 2020
- Study start6 May 2021
- Primary completion22 May 2023
- Study completion22 May 2023
Why it stopped: The trial was terminated prematurely as it met pre-defined criteria for futility at IA3.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Active Systemic Lupus ErythematosusStudies of the same condition, open and under way.
- More trials run by AmgenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Amgen
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- MD, Study director, Amgen
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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
Study at a glance
From the registry record, last updated by the sponsor on 28 Jun 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT04680637
- Acronym / sponsor ID
- 20200234
- Conditions
- Active Systemic Lupus Erythematosus
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: The trial was terminated prematurely as it met pre-defined criteria for futility at IA3.
- Enrolment
- 168 participants (actual)
- Lead sponsor
- AmgenIndustry (pharma, biotech, devices)
- Study start
- 6 May 2021 (actual)
- Primary completion
- 22 May 2023 (actual)
- Study completion
- 22 May 2023 (actual)
- First posted
- 23 Dec 2020 (actual)
- Results
- Posted 28 Jun 2024
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective is to evaluate the efficacy and safety of efavaleukin alfa in subjects with active systemic lupus erythematosus.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Placebo + Standard of Care | Placebo comparator | Drug: Placebo, Other: Standard of Care |
| Efavaleukin Alfa Dose Level One + Standard of Care | Experimental | Drug: Efavaleukin Alfa, Other: Standard of Care |
| Efavaleukin Alfa Dose Level Two + Standard of Care | Experimental | Drug: Efavaleukin Alfa, Other: Standard of Care |
| Efavaleukin Alfa Dose Level Three + Standard of Care | Experimental | Drug: Efavaleukin Alfa, Other: Standard of Care |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- 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.
Key exclusion criteria (31 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Efavaleukin AlfaAlso: AMG 592Administered as a subcutaneous (SC) injection. | Drug | Efavaleukin Alfa Dose Level One + Standard of Care, Efavaleukin Alfa Dose Level Three + Standard of Care, Efavaleukin Alfa Dose Level Two + Standard of Care |
| PlaceboAdministered as a subcutaneous (SC) injection. | Drug | Placebo + Standard of Care |
| Standard of CareStandard of care procedures and therapies for managing active systemic lupus erythematosus will be carried out according to each investigator's standard procedures. | Other | Efavaleukin Alfa Dose Level One + Standard of Care, Efavaleukin Alfa Dose Level Three + Standard of Care, Efavaleukin Alfa Dose Level Two + Standard of Care, Placebo + Standard of Care |
Primary outcome
Number of Participants Who Achieved a Systemic Lupus Erythematosus Responder Index 4 (SRI-4) Response at Week 52
Time frame: 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.
30 secondary outcomes
Number of Participants Who Achieved a BILAG-based Composite Lupus Assessment (BICLA) Response at Week 52
Time frame: Week 52
Number of Participants Who Achieved a Lupus Low Disease Activity State (LLDAS) Response at Week 52
Time frame: Week 52
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
Time frame: Baseline to Week 52
Number of Participants Who Achieved a SRI-4 Response at Week 24
Time frame: Week 24
Number of Participants Who Achieved a BICLA Response at Week 24
Time frame: Week 24
Number of Participants With a hSLEDAI Response at Week 24 and Week 52
Time frame: Week 24 and Week 52
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
Time frame: Weeks 8, 12, 24, 36 and 52
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
Time frame: Weeks 8, 12, 24, 36 and 52
Annualized Flare Rate Over 52 Weeks
Time frame: Up to 52 weeks
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
Time frame: Baseline to Week 12, 24, 36 and 52
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
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Mental Component Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Physical Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Social Role Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Physical Role Functioning Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Bodily Pain Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Mental Health Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Emotional Role Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Vitality Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the General Health Domain Score of the SF-36V2 at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Physical Health Domain Score of the Lupus Quality of Life (LupusQoL) at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Pain Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Planning Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Intimate Relationship Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Burden to Others Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Emotional Health Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Body Image Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Change From Baseline in the Fatigue Domain Score of the LupusQoL at Week 12, 24, 36 and 52
Time frame: Baseline to Week 12, 24, 36 and 52
Number of Participants Who Experienced a Treatment-emergent Adverse Event (TEAE)
Time frame: Day 1 to Week 56
Serum Efavaleukin Alfa Concentrations by Timepoint
Time frame: 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
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jun 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 37491104Garces 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.
- AmgenTrials clinical trials websiteLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
MD study director
Amgen
150 sites in 19 countries: see every site and its status.
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.