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.
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.
Show all 22Show fewer
- 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
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
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
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
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
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
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
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
Belgium3 sites
Teva Investigational Site 102
Brussels, 1090
Teva Investigational Site 101
Liège, 4000
Teva Investigational Site 100
Yvoir, 5530
Hungary3 sites
Teva Investigational Site 501
Budapest, 1023
Teva Investigational Site 502
Debrecen, 4032
Teva Investigational Site 500
Zalaegerszeg, 8900
Spain3 sites
Teva Investigational Site 751
Dresden, 01307
Teva Investigational Site 752
Santander, 39008
Teva Investigational Site 750
Seville, 41013
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.
- Conditions
- Systemic Lupus Erythematosus
- 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 group | Role | What they receive |
|---|---|---|
| CEP-33457 | Experimental | Participants 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 |
| Placebo | Placebo comparator | Participants 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.
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)
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
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
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
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
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
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
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
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
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
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.
- First posted2 Jun 2010 (estimated)
- Study start24 Jun 2010
- Primary completion31 Jan 2012
- Study completion30 Jun 2012
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.
- Other trials for Systemic Lupus ErythematosusStudies of the same condition, open and under way.
- 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
- 183 participants (actual)
Sponsor and investigators
- Lead sponsor
- Cephalon, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Teva Medical Expert, Study director, Teva Branded Pharmaceutical Products R&D, Inc.
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
- Results posted
- Yes, on ClinicalTrials.gov
Study at a glance
From the registry record, last updated by the sponsor on 16 Dec 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT01135459
- Acronym / sponsor ID
- C33457/2047
- Conditions
- Systemic Lupus Erythematosus
- Keywords
- Lupus
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 183 participants (actual)
- Lead sponsor
- Cephalon, Inc.Industry (pharma, biotech, devices)
- Study start
- 24 Jun 2010 (actual)
- Primary completion
- 31 Jan 2012 (actual)
- Study completion
- 30 Jun 2012 (actual)
- First posted
- 2 Jun 2010 (estimated)
- Results
- Posted 16 Dec 2022
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 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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| CEP-33457 | Experimental | Drug: CEP-33457Participants will receive CEP-33457 200 mcg SC every 4 weeks for 20 weeks (Day 1, Weeks 4, 8, 12, 16, and 20). |
| Placebo | Placebo comparator | Drug: PlaceboParticipants will receive placebo matching to CEP-33457 SC every 4 weeks for 20 weeks (Day 1, Weeks 4, 8, 12, 16, and 20). |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- 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.
Key exclusion criteria (22 listed)
- 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).
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 |
|---|---|---|
| CEP-33457Also: LupuzorCEP-33457 will be administered per dose and schedule specified in the arm description. | Drug | CEP-33457 |
| PlaceboPlacebo matching to CEP-33457 will be administered per schedule specified in the arm description. | Drug | Placebo |
Primary outcome
Number of Participants Achieving a Combined Clinical Response Using the Systemic Lupus Erythematosus (SLE) Responder Index (SRI) at Week 24
Time frame: 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.
10 secondary outcomes
Number of Participants Achieving an SRI Response at Each Visit During the Treatment Period
Time frame: Weeks 4, 8, 12, 16, and 20
Number of Participants Achieving a Reduction of at Least 4 Points in the SLEDAI-2K Total Score
Time frame: Week 24
Number of Participants Achieving a British Isles Lupus Assessment Group (BILAG) 2004 Response
Time frame: Weeks 4, 8, 12, 16, 20, and 24
Number of Participants Achieving a BILAG 2004 Clinical Response
Time frame: Weeks 4, 8, 12, 16, 20, and 24
Number of Participants Achieving a Physician Global Assessment (PhGA) Response
Time frame: Weeks 4, 8, 12, 16, 20, and 24
Number of Participants Achieving a Patient's Global Assessment (PtGA) Response
Time frame: Weeks 4, 8, 12, 16, 20, and 24
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
Time frame: Baseline, Week 12, Week 24
Change From Baseline in the Medical Outcome Survey SF-36 Patient-Reported Questionnaire For Mental Component Summary (MCS) Score at Weeks 12 and 24
Time frame: Baseline, Week 12, Week 24
Systemic Lupus International Collaborative Clinics/American College of Rheumatology (SLICC/ACR) Damage Index
Time frame: Baseline, Week 24
Number of Participants With Adverse Events (AEs)
Time frame: Baseline up to Week 24
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Dec 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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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.
Teva Medical Expert study director
Teva Branded Pharmaceutical Products R&D, Inc.
86 sites in 11 countries: see every site and its status.
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.