Canakinumab for Treatment of Adult-onset Still's Disease

Phase 2TerminatedNCT02204293

Charite University, Berlin, Germany36 enrolled

Overview

The purpose of this trial is to investigate the efficacy of the treatment with canakinumab in participants with Adult-onset Still's Disease (AOSD) and active joint involvement.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Adult-Onset Still´s Disease

Interventions

CanakinumabDRUG

Canakinumab, single-dose 4 mg/kg up to 300 mg administered subcutaneously.

PlaceboDRUG

Matching placebo administered subcutaneously.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Written and signed consent from the participant to take part in the study 2. Men and women aged ≥ 18 years and ≤ 75 years 3. Fulfilment of AOSD classification criteria (according to Yamaguchi et al, J. Rheumatology, 1992) 4. Disease activity based on Disease Activity Score 28 (DAS28) of ≥3.2 at screening 5. At least 4 painful and 4 swollen joints at screening and baseline (of the 28 joints according to DAS28) 6. If undergoing treatment with non-steroidal anti-inflammatory drugs (NSAIDs), stable dose for at least 4 weeks prior to randomisation 7. If undergoing treatment with glucocorticoids, stable dose of ≤10 milligrams per day (mg/day) (prednisolone or equivalent) for at least 4 weeks prior to randomisation 8. If undergoing treatment with conventional disease-modifying anti-rheumatic drugs (DMARD), stable dose for at least 3 months prior to randomisation 9. Normalisation period for biological DMARDS (anakinra 1 week, etanercept 1 month, adalimumab and certolizumab 2 months, infliximab, golimumab, abatacept and tocilizumab 3 months, rituximab 9 months, canakinumab 6 months) prior to randomisation 10. In participants of reproductive age, use of an effective method of contraception as well as negative pregnancy test prior to the study commencing. Exclusion Criteria: 1. Previous treatment with the study drug with repeated administration of canakinumab 2. Intraarticular or intravenous administration of glucocorticoids within 4 weeks prior to the baseline or use of narcotic analgesics except for analgesics permitted within the framework of the investigation (codeine and tramadol) 3. Presence of another, serious chronic-inflammatory disease 4. Positive hepatitis B antigen (HBsAg), hepatitis C antibodies and/or human immunodeficiency virus (HIV) antibodies. 5. Presence of a relevant, active infection or other diseases, which entail a tendency towards infection 6. Positive screening for latent tuberculosis, in accordance with usual local practice 7. Raised liver count (raised bilirubin; alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 3-fold the normal range) 8. Serum-creatinine concentration \>1.5 milligrams per deciliter (mg/dL) 9. Inadequate haematological findings (hemoglobin \[Hb\] ≤ 10 grams per deciliter (g/dL), neutrophils ≤2,500/microliter (µl) and thrombocytes ≤100,000/µl) 10. Simultaneous participation in any other interventional clinical study within the last 30 days preceding the commencement of the study 11. History of neoplasia with the exception of a curatively treated non-melanoma skin tumour or carcinoma of the cervix treated in situ without any indication of recurrence within the last 10 years 12. Relevant cardiac or pulmonary disorders 13. Severe intercurrent neurological or psychiatric disorders 14. Macrophage activation syndrome (MAS) as part of previous treatment with IL-1 blockade (e.g. anakinra, rilonacept) 15. Vaccination with a live vaccine within 3 months before the baseline 16. Alcohol or drug abuse in the past 12 months 17. ≥400 milliliter (mL) donation of blood or loss up to 8 weeks before the baseline 18. Pregnancy or breast-feeding 19. Commitment of the patient to an institution at the direction of an authority or court

Locations (14)

Charité Campus Mitte

Berlin, Germany

Immanuel Krankenhaus Berlin

Berlin, Germany

Med. Klinik I für Innere Medizin Köln

Cologne, Germany

Outcomes

Primary Outcomes

Core Study Part I: Percentage of Responders as Assessed by Disease Activity Score 28 Joints (DAS28) Score at Week 12

Responders included participants with change in disease activity score based on 28 joint counts and ESR (DAS28) score \> 1.2. The DAS28 score index is a composite score of weighted components including tender joint counts of 28, swollen joint counts of 28, patient global assessment of disease activity score, and the erythrocyte sedimentation rate (ESR) value. Total score ranged between 0-10. A DAS28-ESR score of 5.1 or above = high disease activity, a value between 3.2 and 5.1 = moderate disease activity and value between 2.6 and 3.2 = low disease activity, value \< 2.6 = disease remission.

Time frame: Week 12

Secondary Outcomes

Core Study Part I: Change From Baseline (CFB) in Disease Activity Score 28 Joints Erythrocyte Sedimentation Rate (DAS28 [ESR]) Score

The DAS28 index is a composite score of weighted components including tender joint counts of 28, swollen joint counts of 28, patient global assessment of disease activity score, and ESR value.Total score ranged between 0-10. A DAS28-ESR score of 5.1 or above = high disease activity, a value between 3.2 and 5.1 = moderate disease activity and value between 2.6 and 3.2 = low disease activity, value \< 2.6 = disease remission. A positive change in score indicates worsening, and a negative change indicates improvement. Least squares (LS) mean was calculated by mixed linear model for repeated measures (MMRM) analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in DAS28 C-reactive Protein (CRP) Score

The DAS28 index is a composite score of weighted components including tender joint counts of 28, swollen joint counts of 28, patient global assessment of disease activity score, and CRP value. Total score ranged between 0-10. A DAS28-CRP score of 5.1 or above = high disease activity, a value between 3.2 and 5.1 = moderate disease activity and value between 2.6 and 3.2 = low disease activity, value \< 2.6 = disease remission. A positive change in score indicates worsening, and a negative change indicates improvement. LS mean was calculated by MMRM analyses.

Data from ClinicalTrials.gov

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Universität Erlangen

Erlangen, Germany

Kliniken Essen-Süd/Krankenhaus St. Josef

Essen, Germany

Universitätsklinikum der J.W. Goethe-Universität Frankfurt

Frankfurt A. M., Germany

Asklepios Klinikum Hamburg Altona

Hamburg, Germany

Medizinische Hochschule Hannover

Hanover, Germany

Universitätsklinikum Heidelberg

Heidelberg, Germany

Universitätskrankenhaus Schleswig Holstein

Kiel, Germany

...and 4 more locations

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in American College of Rheumatology (ACR) Component: 68 Tender Joint Count (TJC)

The 68 TJC included the 8 distal interphalangeal (IP), 10 proximal IP and 10 metacarpophalangeal (MTP) joints of hands, the 10 MTP and 10 proximal IP joints of feet, the 2 wrists, 2 elbows, 2 shoulders, 2 acromioclavicular, 2 sternoclavicular, 2 temporomandibular, 2 hip, 2 knee, 2 talo-tibial, and 2 mid-tarsal joints. Joint tenderness was graded present (1) or absent (0). Total score is calculated by adding the scores, which range from 0 (no tender joint) to 68 (all tender joints). Lower scores indicate no tender joint and higher scores indicate worsening tender joints. A negative change from Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in ACR Component: 66 Swollen Joint Count (SJC)

The 66 SJC included the 8 distal interphalangeal (IP), 10 proximal IP and 10 metacarpophalangeal (MTP) joints of hands, the 10 MTP and 10 proximal IP joints of feet, the 2 wrists, 2 elbows, 2 shoulders, 2 acromioclavicular, 2 sternoclavicular, 2 temporomandibular, 2 knee, 2 talo-tibial, and 2 mid-tarsal joints. Swelling was graded present (1) or absent (0). Total score is calculated by adding the scores, which range from 0 (no swollen joint) to 66 (all swollen joints). Lower scores indicate no swollen joint and higher scores indicate worsening swollen joints. A negative change in Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in the 28 TJC

A total of 28 joints were assessed for tenderness. The number of tender joints could range from 0 to 28, where higher values represented more tender joints. The change from Baseline to any time points was averaged among all participants, where negative changes indicated an improvement in disease activity. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in the 28 SJC

A total of 28 joints were assessed for swelling. The number of swollen joints could range from 0 to 28, where higher values represented more swollen joints. The change from Baseline to any time point was averaged among all participants, where negative changes indicated an improvement in disease activity. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in ACR Component: Acute Phase Reactant CRP

A negative change from Baseline in CRP level indicates an improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in ACR Component: Acute Phase Reactant ESR

A negative change from Baseline in ESR level indicates an improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in Serum Ferritin Level at Week 12

LS mean was calculated by MMRM analyses.

Time frame: Week 12

Core Study Part I: Percentage of Responders With Fever Episodes

Fever is defined as an oral or rectal body temperature greater than 38 degrees Celsius (°C).

Time frame: Week 12

Core Study Part I: CFB in ACR Component: Physician's Global Assessment of Disease Activity Score

The physician's global assessment of disease activity was assessed using a numerical rating scale of 0-10 where 0= no disease activity and 10= activity to maximal disease activity. A negative change from Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in ACR Component: Participant's Global Assessment of Disease Activity Score

The participant's global assessment of disease activity was assessed using a numerical rating scale of 0-10, where 0= no disease activity and 10= maximal disease activity. A negative change from Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in ACR Component: Participant's Global Assessment of Pain Score

The participant's global assessment of pain was assessed using a numerical rating scale of 0-10, where 0= no disease activity and 10= maximal disease activity. A negative change from Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Weeks 4, 8 and 12

Core Study Part I: CFB in Health Assessment Questionnaire-Disability Index (HAQ-DI) Score

The HAQ measures physical disability and functional status. It has 4 dimensions: disability, pain, drug side effects and dollar costs. The HAQ score is calculated by summing the computed scores for each category and dividing by the number of categories answered. It ranges from 0 (without any difficulty) to 3 (unable to do). A negative change from Baseline indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With American College of Rheumatology Response of 20 (ACR20)

ACR20 response was defined as a ≥ 20% improvement (reduction) compared with Baseline for both 68 TJC and 66 SJC, as well as for three of the additional five ACR core set variables: Participant's Assessment of Pain over the previous 24 hours: using a NRS left end of the line 0=no pain to right end of the line 10=unbearable pain; Participant's Global Assessment of Disease Activity and Physician's Global Assessment of Disease Activity over the previous 24 hours using a NRS where left end of the line 0=no disease activity to right end of the line 10=maximum disease activity; HAQ-DI 20 questions, 8 components: dressing/grooming, arising, eating, walking, hygiene, reach, grip and activities, 0=without difficulty to 3=unable to do; and acute-phase reactant ESR.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With ACR30

ACR30 response was defined as a ≥ 30% improvement (reduction) compared with Baseline for both 68 TJC and 66 SJC, as well as for three of the additional five ACR core set variables: Participant's Assessment of Pain over the previous 24 hours: using a NRS left end of the line 0=no pain to right end of the line 10=unbearable pain; Participant's Global Assessment of Disease Activity and Physician's Global Assessment of Disease Activity over the previous 24 hours using a NRS where left end of the line 0=no disease activity to right end of the line 10=maximum disease activity; HAQ 20 questions, 8 components: dressing/grooming, arising, eating, walking, hygiene, reach, grip and activities, 0=without difficulty to 3=unable to do; and acute-phase reactant ESR.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With Modified ACR30

A participant was considered responder if he/she had achieved the incidence of modified adapted response (ACR30 criteria) of at least a 30% improvement in no intermittent fever and had at least 30% improvement in at least 6 of the following 7 measures: tender and swollen 68-joint counts, participant's assessment of pain, participant's global assessment of disease activity, physician's global assessment of disease activity, participant's functional capacity (HAQ-DI score) and acute phase reactant- ESR. Participant were modified ACR30 responders at a given post-randomization visit if they satisfied the modified ACR30 criteria, respectively.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With ACR50

ACR50 response was defined as a ≥ 50% improvement (reduction) compared with Baseline for both 68 TJC and 66 SJC, as well as for three of the additional five ACR core set variables: Participant's Assessment of Pain over the previous 24 hours: using a NRS left end of the line 0=no pain to right end of the line 10=unbearable pain; Participant's Global Assessment of Disease Activity and Physician's Global Assessment of Disease Activity over the previous 24 hours using a NRS where left end of the line 0=no disease activity to right end of the line 10=maximum disease activity; HAQ-DI 20 questions, 8 components: dressing/grooming, arising, eating, walking, hygiene, reach, grip and activities, 0=without difficulty to 3=unable to do; and acute-phase reactant ESR.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With ACR70

ACR70 response was defined as a ≥ 70% improvement (reduction) compared with Baseline for both 68 TJC and 66 SJC, as well as for three of the additional five ACR core set variables: Participant's Assessment of Pain over the previous 24 hours: using a NRS left end of the line 0=no pain to right end of the line 10=unbearable pain; Participant's Global Assessment of Disease Activity and Physician's Global Assessment of Disease Activity over the previous 24 hours using a NRS where left end of the line 0=no disease activity to right end of the line 10=maximum disease activity; HAQ-DI 20 questions, 8 components: dressing/grooming, arising, eating, walking, hygiene, reach, grip and activities, 0=without difficulty to 3=unable to do; and acute-phase reactant ESR.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With ACR90

ACR90 response was defined as a ≥ 90% improvement (reduction) compared with Baseline for both 68 TJC and 66 SJC, as well as for three of the additional five ACR core set variables: Participant's Assessment of Pain over the previous 24 hours: using a NRS left end of the line 0=no pain to right end of the line 10=unbearable pain; Participant's Global Assessment of Disease Activity and Physician's Global Assessment of Disease Activity over the previous 24 hours using a NRS where left end of the line 0=no disease activity to right end of the line 10=maximum disease activity; HAQ-DI 20 questions, 8 components: dressing/grooming, arising, eating, walking, hygiene, reach, grip and activities, 0=without difficulty to 3=unable to do; and acute-phase reactant ESR.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders With European League Against Rheumatism (EULAR) Response

EULAR response is based on DAS28-ESR and DAS28-CRP scores. The DAS28 index is a composite score of weighted components including tender joint counts of 28, swollen joint counts of 28, subject global assessment of disease activity score, and ESR or CRP value. A DAS28-CRP or ESR score of 5.1 or above = high disease activity, a value between 3.2 and 5.1 = moderate disease activity and value between 2.6 and 3.2 = low disease activity, value \< 2.6 = disease remission. EULAR response has 3 categories: EULAR Good response: DAS28 ≤ 3.2 and a change from Baseline \< -1.2. EULAR Moderate response: DAS28 \>3.2 to ≤ 5.1 or a change from Baseline \< -0.6 to ≥ -1.2 or EULAR No response: DAS28 \>5.1 or a change from Baseline \< -0.6 to ≤ -1.2.

Time frame: Baseline, Week 12

Core Study Part I: Percentage of Responders Achieving Low Disease Activity (LDA)

Percentage of responders were defined as the participants who achieved LDA (DAS28 score \< 3.2) at Week 12. The DAS28 index is a composite score of weighted components including tender joint counts of 28, swollen joint counts of 28, participant global assessment of disease activity score, and ESR or CRP value. Total score ranged between 0-10. A DAS28 score greater than 5.1 implies high disease activity, equal to or less than 3.2 low disease activity, and less than 2.6 remissions.

Time frame: Week 12

Core Study Part I: Percentage of Responders Achieving Disease Remission and Extended Disease Remission

Participants with disease remission: LDA (DAS28 score\< 2.6). The DAS28 index is a composite score of weighted components including both 28 TJC an SJC, participant global assessment of disease activity score, and ESR or CRP value. A DAS28 score greater than 5.1: high disease activity, ≤ 3.2: low disease activity, and less than 2.6: remission. Extended remission criteria included DAS28 \< 2.6 and no signs of systemic activity for up to two consecutive study visits till Week 12 defined as any of Yamaguchi´s primary classification criteria for AOSD which included fever attacks at 39 °C for more than a week, arthralgia, salmon red, maculate, urticarial or maculo-papular rash and leukocytosis (white blood cells increase) of \> 10000/cubic millimeters (mm\^3) with \> 80% neutrophils.

Time frame: Week 12

Core Study Part I: Change in Joint Mobility (Degrees of Motion) Assessed by Neutral Zero Method

Number of joints with limitation of motion according to neutral zero method was assessed which included mobility of joints (elbows, wrists, shoulder joints, hip joints, knee joints, and upper ankle joints) within the reference range/degree. Response is defined as an improvement of ≥ 30%, 50%, 70% and 90% from Baseline. A negative change score indicates improvement. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Week 12

Core Study Part I: CFB in Medical Outcome Short Form (SF-36) Health Survey Score

The SF-36 determines overall quality of life assessing 1) limitations in physical functioning due to health problems; 2) limitations in usual role because of physical health problems; 3) bodily pain; 4) general health perceptions; 5) vitality; 6) limitations in social functioning because of physical or emotional problems; 7) limitations in usual role due to emotional problems; and 8) general mental health. Items 1-4 contribute to physical component summary score (PCS). Items 5-8 contribute to mental component summary score (MCS). Scores on each item are summed and averaged (range = 0 "worst"-100 "best"). Positive numbers indicate improvement from Baseline. LS mean was calculated by MMRM analyses.

Time frame: Baseline, Week 12

Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)

An AE is an adverse medical event which occurs in a participant of the study and which is not necessarily in a causal relationship with the treatment the participant receives. AEs include symptoms of illnesses, as well as every unfavourable and unintended reaction. SAEs are AEs leading to death, are life-threatening, require hospitalizations or prolongation of hospitalizations, represent an innate malformation or a congenital abnormality.

Time frame: Up to Month 27