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Systemic Lupus ErythematosusPhase 2NCT01135459

A Study to Evaluate the Efficacy and Safety of CEP-33457 in Participants With Systemic Lupus Erythematosus (SLE)

A Phase 2 study testing CEP-33457 in people with Systemic Lupus Erythematosus, run by Cephalon, Inc. at 86 sites in 11 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary objective of this study is to evaluate the efficacy of a 200 micrograms (mcg) dose of CEP-33457 compared with placebo in participants with active systemic lupus erythematosus (SLE) as assessed by the proportion of participants achieving a combined clinical response using the SLE responder index (SRI) at… Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Systemic Lupus Erythematosus
What is being tested?
CEP-33457
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
183 participants
Where
86 sitesin 11 countries
Study dates
24 Jun 2010to 30 Jun 2012
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 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • The participant has an established diagnosis of systemic lupus erythematosus (SLE) as defined by ACR Classification Revised Criteria. The diagnosis is fulfilled provided that at least 4 criteria are met.
  • The participant has a positive test for antinuclear antibody (ANA) at screening and/or a positive test for anti-double-stranded deoxyribonucleic acid antibody (anti-dsDNA Ab) at screening.
  • Women must be surgically sterile, 2 years postmenopausal, or, if of childbearing potential, using a medically accepted method of contraception, and must agree to continued use of this method for the duration of the study and for 30 days after discontinuation of study drug treatment.
  • The participant has a clinical SLEDAI-2K score of at least 6 points during screening.
  • The participant does not have an "A" score on the BILAG-2004 scale.
  • If the patient is using oral corticosteroids, the weekly cumulative dose must not exceed 80 mg of prednisone equivalent; the weekly dose must be stable over the 4 weeks preceding the first dose of study drug.
  • If the participant is using antimalarials, methotrexate, leflunomide, mycophenolate mofetil, or azathioprine, the start date must be at least 3 months prior to the first dose of study drug, and the daily dose must be stable over the 4 weeks preceding the first dose of study drug.
  • If the participant is not currently using corticosteroids, antimalarials, methotrexate, mycophenolate mofetil, or azathioprine, the last dose (in case of previous use) must be at least 4 weeks prior to the first dose of study drug. For leflunomide, the stop date must be at least 8 weeks before the first dose of study drug, unless an adequate cholestyramine washout has been completed.

Who cannot join

  • The participant has been treated with intramuscular or intravenous (iv) pulse steroids (ie, 250 to 1000 milligrams [mg] iv total daily dose of methylprednisolone) within 4 weeks of the first dose of study drug. The use of intra-articular steroids may be allowed after consultation with the medical expert.
  • The participant has received tacrolimus, cyclosporine A, or iv immunoglobulins (IVIG) within 3 months of the first dose of study drug.
  • The participant has received cyclophosphamide within 12 months prior to the first dose of study drug.
  • The participant has been treated for SLE with agents such as fusion proteins, therapeutic proteins, or monoclonal antibodies or antibody fragments, within 12 months of the first dose of study drug.
  • The participant has received B-cell depleting agents such as rituximab and has not yet normalized the B-cell count (ie, CD20+ B-cell count is less than 200 and the absolute lymphocyte count [ALC] is less than 1500/μL).
  • The participant has New York Heart Association (NYHA) Class III or IV congestive heart failure.
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  • The participant has severe active lupus nephritis or cerebritis.
  • The participant has an estimated glomerular filtration rate (eGFR) of less than 30 milliliters (mL)/minute (min)/1.73 square meter (m^2) (via Modification of Diet in Renal Disease [MDRD] equation).
  • The participant has an aspartate aminotransferase (AST) or alanine aminotransferase (ALT) value greater than 2 times the upper limit of normal (ULN) or a total bilirubin level greater than 1.5 times ULN.
  • The participant has a planned immunization with a live or live attenuated vaccine within 3 months prior to administration of the first dose of study drug and for 3 months after administration of the last dose of study drug.
  • The participant has any clinically significant abnormalities on electrocardiogram (ECG) that are not related to SLE, as determined by the investigator. Participant with stable ECG changes without evidence of active cardiovascular disease may participate at the discretion of the investigator and medical monitor.
  • The participant has an ongoing active systemic infection requiring treatment or a history of severe infection, such as hepatitis or pneumonia, in the 3 months prior to administration of the first dose of study drug. Less severe infections in the 3 months prior to administration of the first dose of study drug are permitted at the discretion of the investigator and medical monitor.
  • The participant has any concomitant medical condition unrelated to SLE that may interfere with his or her safety or with evaluation of the study drug, as determined by the investigator.
  • The participant has a history of a medical condition other than SLE that has required treatment with steroids in excess of 80 mg of prednisone equivalent/week within 6 months of the first dose of study drug.
  • The participant has a positive test result for hepatitis B surface antigen (HBsAg) or antibodies to hepatitis C (HCV Ab).
  • The participant has a known positive history of antibodies to human immunodeficiency virus (HIV) or HIV disease.
  • The participant has a history of alcohol or substance dependence or abuse (with the exception of nicotine), according to the Diagnostic and Statistical Manual of Mental Disorders of the American Psychiatric Association, Fourth Edition, Text Revision (DSM-IV-TR), within 3 months of the screening visit or has current substance abuse.
  • The participant has a history of severe allergic reactions to or hypersensitivity to any component of the study drug or placebo.
  • The participant has undergone or is undergoing treatment with another investigational drug for the treatment of lupus within 6 months prior to the 1st dose of study drug or has received any other investigational drug for any other condition within 30 days prior to the 1st dose of study drug.
  • The participant has previously participated in a Cephalon- or ImmuPharma-sponsored clinical study with CEP-33457.
  • The participant is a pregnant or lactating woman. (Any women becoming pregnant during the study will be withdrawn from the study.)
  • The participant is unlikely to comply with the study protocol or is unsuitable for any other reason, as judged by the investigator or medical monitor.

Trial locations and contacts

86 sites in 11 countries.

86 sites in 11 countries

United States40 sites
  • Teva Investigational Site 22

    Ann Arbor, Michigan, 48109

  • Teva Investigational Site 19

    Arlington, Virginia, 22205

  • Teva Investigational Site 8

    Atlanta, Georgia, 30322

  • Teva Investigational Site 31

    Atlanta, Georgia, 30342

  • Teva Investigational Site 30

    Aurora, Colorado, 80045

  • Teva Investigational Site 4

    Aventura, Florida, 33180

  • Teva Investigational Site 36

    Baltimore, Maryland, 21231

  • Teva Investigational Site 27

    Birmingham, Alabama, 35233

  • Teva Investigational Site 10

    Boston, Massachusetts, 02111

  • Teva Investigational Site 3

    Chapel Hill, North Carolina, 27599-7600

  • Teva Investigational Site 15

    Charleston, South Carolina, 29425

  • Teva Investigational Site 28

    Charlotte, North Carolina, 28210

  • Teva Investigational Site 32

    Clearwater, Florida, 33765

  • Teva Investigational Site 23

    Coeur d'Alene, Idaho, 83814

  • Teva Investigational Site 29

    Dallas, Texas, 75231

  • Teva Investigational Site 25

    Duncansville, Pennsylvania, 16635

  • Teva Investigational Site 18

    Durham, North Carolina, 27710

  • Teva Investigational Site 35

    Fort Lauderdale, Florida, 33334

  • Teva Investigational Site 40

    Houston, Texas, 77034

  • Teva Investigational Site 6

    Houston, Texas, 77074

  • Teva Investigational Site 1

    Jupiter, Florida, 33458

  • Teva Investigational Site 37

    Lexington, Kentucky, 40504

  • Teva Investigational Site 16

    Los Angeles, California, 90048

  • Teva Investigational Site 5

    Los Angeles, California, 90095-1769

  • Teva Investigational Site 9

    Manhasset, New York, 11030

  • Teva Investigational Site 39

    Mesquite, Texas, 75150

  • Teva Investigational Site 33

    Milwaukee, Wisconsin, 53226

  • Teva Investigational Site 2

    Monroe, North Carolina, 28112

  • Teva Investigational Site 21

    Oklahoma City, Oklahoma, 73103

  • Teva Investigational Site 13

    Oklahoma City, Oklahoma, 73104

  • Teva Investigational Site 26

    Pittsburgh, Pennsylvania, 15213

  • Teva Investigational Site 34

    San Antonio, Texas, 78229

  • Teva Investigational Site 7

    San Diego, California, 92161

  • Teva Investigational Site 14

    San Leandro, California, 94578

  • Teva Investigational Site 12

    Seattle, Washington, 98104

  • Teva Investigational Site 17

    Stanford, California, 94305

  • Teva Investigational Site 38

    Stockbridge, Georgia, 30281

  • Teva Investigational Site 11

    Tampa, Florida, 33614

  • Teva Investigational Site 24

    Temple, Texas, 76508

  • Teva Investigational Site 20

    Tucson, Arizona, 85715

Other trials in United States

Germany7 sites
  • Teva Investigational Site 402

    Aachen, 52074

  • Teva Investigational Site 403

    Berlin, 12200

  • Teva Investigational Site 401

    Dresden, 01307

  • Teva Investigational Site 404

    Düsseldorf, 40225

  • Teva Investigational Site 406

    Hamburg, 22081

  • Teva Investigational Site 405

    Mainz, 55131

  • Teva Investigational Site 400

    München, 80336

Other trials in Germany

Poland7 sites
  • Teva Investigational Site 603

    Dąbrówka, 62-069

  • Teva Investigational Site 600

    Elblag, 82-300

  • Teva Investigational Site 602

    Gmina Końskie, 26-200

  • Teva Investigational Site 604

    Lublin, 20-090

  • Teva Investigational Site 601

    Lublin, 20-607

  • Teva Investigational Site 606

    Warsaw, 00-235

  • Teva Investigational Site 605

    Wroclaw, 50-556

Other trials in Poland

Ukraine6 sites
  • Teva Investigational Site 901

    Donetsk, 83059

  • Teva Investigational Site 905

    Ivano-Frankivsk, 76018

  • Teva Investigational Site 900

    Kyiv, 01601

  • Teva Investigational Site 902

    Kyiv, 03151

  • Teva Investigational Site 903

    Kyiv, 04107

  • Teva Investigational Site 904

    Lviv, 79035

Other trials in Ukraine

France5 sites
  • Teva Investigational Site 301

    Lille, 59000

  • Teva Investigational Site 302

    Nantes, 44093

  • Teva Investigational Site 300

    Paris, 75013

  • Teva Investigational Site 303

    Paris, 75674

  • Teva Investigational Site 304

    Strasbourg, 67098

Other trials in France

Czechia4 sites
  • Teva Investigational Site 201

    Brno, 638 00

  • Teva Investigational Site 200

    Olomouc, 775 20

  • Teva Investigational Site 202

    Prague, 128 08

  • Teva Investigational Site 203

    Prague, 128 50

Other trials in Czechia

Portugal4 sites
  • Teva Investigational Site 701

    Amadora, 2720-276

  • Teva Investigational Site 702

    Coimbra, 3000-075

  • Teva Investigational Site 703

    Porto, 4099-001

  • Teva Investigational Site 700

    Porto, 4200-319

Other trials in Portugal

United Kingdom4 sites
  • Teva Investigational Site 803

    Bath, BA1 1RL

  • Teva Investigational Site 801

    Leeds, LS7 4SA

  • Teva Investigational Site 800

    London, SE1 7EH

  • Teva Investigational Site 802

    Newcastle upon Tyne, NE7 7DN

Other trials in United Kingdom

Belgium3 sites
  • Teva Investigational Site 102

    Brussels, 1090

  • Teva Investigational Site 101

    Liège, 4000

  • Teva Investigational Site 100

    Yvoir, 5530

Other trials in Belgium

Hungary3 sites
  • Teva Investigational Site 501

    Budapest, 1023

  • Teva Investigational Site 502

    Debrecen, 4032

  • Teva Investigational Site 500

    Zalaegerszeg, 8900

Other trials in Hungary

Spain3 sites
  • Teva Investigational Site 751

    Dresden, 01307

  • Teva Investigational Site 752

    Santander, 39008

  • Teva Investigational Site 750

    Seville, 41013

Other trials in Spain

About this study

Official title: A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a 200-mcg Dose of CEP-33457 in Patients With Systemic Lupus Erythematosus

The primary objective of this study is to evaluate the efficacy of a 200 micrograms (mcg) dose of CEP-33457 compared with placebo in participants with active systemic lupus erythematosus (SLE) as assessed by the proportion of participants achieving a combined clinical response using the SLE responder index (SRI) at Week 24.

Read the detailed description

The study consisted of a 2-week screening period (visit 1), a 20-week treatment period beginning with a baseline visit in which randomization was completed and study drug treatment began (visits 2 through 7), and a final assessment was performed 4 weeks after the last dose of study drug (visit 8 [week 24 or early termination]). Participants were randomized to receive either CEP-33457 or placebo subcutaneously (SC) every 4 weeks. Plasma samples for measurement of study drug concentration were collected in a subset of participants and study drug was administered at each study visit until the final visit. The dose of background steroid medication may have been increased, if needed, to treat the participant for minor fluctuations in lupus disease activity. One interim analysis was conducted when at least 80 participants completed Week 12 or had been withdrawn from the study. Participants who completed the treatment period returned to the study center 4 weeks after the last dose had been administered for final procedures and assessments. Final procedures and assessments for participants who withdrew from the study before 20 weeks of treatment were performed at the last visit. Final procedures and assessments for participants who participated in the study beyond week 24 were to be performed at the next regularly scheduled visit. Participants who complete the study will be eligible for participation in the 12-month open-label study (study C33457/3075; herein referred to as study 3075) to assess continued effectiveness and safety of the CEP-33457 treatment.

Being tested
CEP-33457, Placebo
Keywords
Lupus
Medical subject headings
Lupus Erythematosus, Systemic

What participants receive

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

  • CEP-33457Drug

    Also called Lupuzor

    CEP-33457 will be administered per dose and schedule specified in the arm description.

  • PlaceboDrug

    Placebo matching to CEP-33457 will be administered per schedule specified in the arm description.

Study groups in NCT01135459
Study groupRoleWhat they receive
CEP-33457ExperimentalParticipants will receive CEP-33457 200 mcg SC every 4 weeks for 20 weeks (Day 1, Weeks 4, 8, 12, 16, and 20).
Receives: Drug: CEP-33457
PlaceboPlacebo comparatorParticipants will receive placebo matching to CEP-33457 SC every 4 weeks for 20 weeks (Day 1, Weeks 4, 8, 12, 16, and 20).
Receives: Drug: Placebo

What is being measured

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

  1. Number of Participants Achieving a Combined Clinical Response Using the Systemic Lupus Erythematosus (SLE) Responder Index (SRI) at Week 24

    An SRI response was defined as a reduction from baseline in SLE Disease Activity Index 2000 (SLEDAI-2K) score of ≥4 points, no worsening in Physician Global Assessment (PhGA), no new British Isles Lupus Assessment Group (BILAG) A body system score, and ≤1 new BILAG B body system score from baseline. SLEDAI-2K includes 24 weighted clinical and laboratory variables. Total score = 0 to 105. A score of 6 to 10 = moderate disease activity, and a reduction of >3 points = improvement. PhGA was completed by physician using a visual analog scale (VAS) from 0=none to 3=severe. A change of >0.3 points = worsening. BILAG includes 97 clinical and laboratory items. Each organ system is assigned a score displayed as a grade from A to E: A=very active disease; B=patient needs increase in treatment for moderately active disease; C=stable or mild disease; D=previous organ involvement but no current disease activity; and E=no current disease activity and organ system has never been involved.

    Measured: Week 24

Secondary outcomes (10)
  1. Number of Participants Achieving an SRI Response at Each Visit During the Treatment Period

    An SRI response was defined as a reduction from baseline in SLEDAI-2K score of ≥4 points, no worsening in PhGA, no new BILAG A body system score, and ≤1 new BILAG B body system score from baseline. SLEDAI-2K includes 24 weighted clinical and laboratory variables. Total score = 0 to 105. A score of 6 to 10 = moderate disease activity, and a reduction of >3 points = improvement. PhGA was completed by physician using a VAS from 0=none to 3=severe. A change of >0.3 points = worsening. BILAG includes 97 clinical and laboratory items. Each organ system is assigned a score displayed as a grade from A to E: A=very active disease; B=participant needs increase in treatment for moderately active disease; C=stable or mild disease; D=previous organ involvement but no current disease activity; and E=no current disease activity and organ system has never been involved.

    Measured: Weeks 4, 8, 12, 16, and 20

  2. Number of Participants Achieving a Reduction of at Least 4 Points in the SLEDAI-2K Total Score

    The SLEDAI-2K is a global index and includes 24 weighted clinical and laboratory variables. The total score (sum of all 24 scores) ranges from 0 to 105. A SLEDAI-2K score of 6 to 10 is indicative of moderate disease activity, and improvement is defined as a reduction of more than 3 points.

    Measured: Week 24

  3. Number of Participants Achieving a British Isles Lupus Assessment Group (BILAG) 2004 Response

    The BILAG 2004 is a validated objective and subjective global measure of the disease activity of SLE based on the physician intention to treat. It includes 97 clinical and laboratory items to evaluate SLE disease activity in 9 organ systems; each organ system is assigned a score displayed as a grade from A to E, as follows: A=very active disease; B=participant needs increase in treatment for moderately active disease; C=stable or mild disease; D=previous organ involvement but no current disease activity; and E=no current disease activity and the organ system has never been involved. BILAG 2004 response was defined as no new A body system score and no more than 1 new BILAG B body system score from baseline.

    Measured: Weeks 4, 8, 12, 16, 20, and 24

  4. Number of Participants Achieving a BILAG 2004 Clinical Response

    The BILAG 2004 is a validated objective and subjective global measure of the disease activity of SLE based on the physician intention to treat. It includes 97 clinical and laboratory items to evaluate SLE disease activity in 9 organ systems; each organ system is assigned a score displayed as a grade from A to E, as follows: A=very active disease; B=participant needs increase in treatment for moderately active disease; C=stable or mild disease; D=previous organ involvement but no current disease activity; and E=no current disease activity and the organ system has never been involved. BILAG 2004 clinical response was defined as having an improvement in at least 1 category from a B score at baseline to a C or D score with no worsening in any other category from baseline.

    Measured: Weeks 4, 8, 12, 16, 20, and 24

  5. Number of Participants Achieving a Physician Global Assessment (PhGA) Response

    The PhGA was completed by the physician using a 3 inch VAS labeled from 0=none to 3=severe. The PhGA response was defined as having no worsening in PhGA (with worsening defined as an increase in PhGA of more than 0.30 inch from baseline).

    Measured: Weeks 4, 8, 12, 16, 20, and 24

  6. Number of Participants Achieving a Patient's Global Assessment (PtGA) Response

    The PhGA was completed by the participant using a 3 inch VAS labeled from 0=none to 3=severe. The PtGA response was defined as having no worsening in PtGA (with worsening defined as an increase in PtGA of more than 0.30 inch from baseline).

    Measured: Weeks 4, 8, 12, 16, 20, and 24

  7. Change From Baseline in the Medical Outcome Survey Short-Form 36 (SF-36) Patient-Reported Questionnaire For Physical Component Summary (PCS) Score at Weeks 12 and 24

    The SF-36 questionnaire has 36 questions composing the scale that represent 8 domains: 1) physical functioning, role physical, 2) bodily pain, 3) general health, 4) vitality, 5) social functioning, 6) role, 7) emotional, and 8) mental health. The scores for the 8 domains were combined into two summary scores: the physical component summary (PCS) score and the mental component summary (MCS) score. Items 1 to 4 primarily contribute to the PCS score of the SF-36. Items 5-8 primarily contribute to the MCS score of the SF-36. Scores on each item were summed and averaged (range: 0=worst to 100=best). Higher scores represent better health status and functional ability.

    Measured: Baseline, Week 12, Week 24

  8. Change From Baseline in the Medical Outcome Survey SF-36 Patient-Reported Questionnaire For Mental Component Summary (MCS) Score at Weeks 12 and 24

    The SF-36 questionnaire has 36 questions composing the scale that represent 8 domains: 1) physical functioning, role physical, 2) bodily pain, 3) general health, 4) vitality, 5) social functioning, 6) role, 7) emotional, and 8) mental health. The scores for the 8 domains were combined into two summary scores: the physical component summary (PCS) score and the mental component summary (MCS) score. Items 1 to 4 primarily contribute to the PCS score of the SF-36. Items 5-8 primarily contribute to the MCS score of the SF-36. Scores on each item were summed and averaged (range: 0=worst to 100=best). Higher scores represent better health status and functional ability.

    Measured: Baseline, Week 12, Week 24

  9. Systemic Lupus International Collaborative Clinics/American College of Rheumatology (SLICC/ACR) Damage Index

    SLICC/ACR score or damage index is a measure of cumulative damage due to SLE. Damage is defined as nonreversible change (not related to active inflammation) occurring since onset of lupus, ascertained by clinical assessment and present for at least 6 months. Damage is defined for 12 separate organ systems: ocular (range 0-2), neuropsychiatric (0-6), renal (0-3), pulmonary (0-5), cardiovascular (0-6), peripheral vascular (0-5), gastrointestinal (0-6), musculoskeletal (0-7), skin (0-3), endocrine (diabetes) (0-1), gonadal (0-1) and malignancies (0-2). A score of 0=no damage, early damage is defined as ≥1. The total maximum score is 47, and increasing score indicates increasing disease damage severity.

    Measured: Baseline, Week 24

  10. Number of Participants With Adverse Events (AEs)

    An AE was defined as any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. SAEs were defined as death, a life-threatening AE, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant disability or incapacity, a congenital anomaly or birth defect, or an important medical event that jeopardized participant and required medical intervention to prevent 1 of the outcomes listed in this definition. A summary of other non-serious AEs and all serious AEs, regardless of causality is located in Reported AE section.

    Measured: Baseline up to Week 24

Timeline

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

  1. First posted2 Jun 2010 (estimated)
  2. Study start24 Jun 2010
  3. Primary completion31 Jan 2012
  4. Study completion30 Jun 2012

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
183 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01135459
Sponsor's protocol ID
C33457/2047
Status last verified
Nov 2022
First submitted
1 Jun 2010
Last updated
16 Dec 2022

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing CEP-33457 in people with Systemic Lupus Erythematosus, run by Cephalon, Inc. at 86 sites in 11 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 8 inclusion and 22 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: finished, as of the sponsor's last update on 16 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 86 sites in United States, Germany, Poland, Ukraine, France and 6 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 16 Dec 2022). 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 Achieving a Combined Clinical Response Using the Systemic Lupus Erythematosus (SLE) Responder Index (SRI) at Week 24 (time frame: Week 24). It is what the study was designed to measure, not a finding.

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

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

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Dec 2022.

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