Ankylosing Spondylitis
Conditions
Keywords
Ankylosing spondylitis, Imaging
Brief summary
This study will evaluate the effectiveness of apremilast in AS as measured by improvement in patients' signs and symptoms of the disease and changes in imaging. Additionally the safety and tolerability of apremilast in AS will be assessed.
Detailed description
Presently, there are very few treatments available which affect the progression of the disease in the spine. The only proven treatment is the use of drugs inhibiting tumour necrosis factor alpha (TNF). However, there are limitations with this treatment in that it needs to be administered via an injection and is also very expensive. Therefore it is necessary to develop new therapeutic agents for this condition. Apremilast (the study drug) is an oral tablet which has been shown to inhibit TNF production in a mouse model of inflammation. It has also been used in clinical trials for asthma and psoriasis in humans with good affect and tolerability. These studies were funded by Celgene Corporation and they will be funding this study. The patients will be recruited from hospitals by Consultant referral. The patients will have had AS for at least 2 years and their symptoms will have been uncontrolled on conventional non-steroidal anti-inflammatory drugs such as ibuprofen. Patients will be randomised to either receive apremilast or a placebo and treated over a period of 12 weeks. They will then be followed up for 28 days after the treatment period.
Interventions
DRUGApremilast
10mg twice a day, dose was titrated by 20mg every 2 days until the maximum dose 30mg twice a day for 12weeks
twice a day
Sponsors
Celgene Corporation
Imperial College London
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Written informed consent to participate in this trial * Diagnosis of ankylosing spondylitis as defined by the modified New York criteria (1984) as follows: 1. a history of inflammatory back pain; 2. limitation of motion of the lumbar spine in both the sagittal and frontal planes; 3. limited chest expansion, relative to standard values for age and sex; 4. definite radiographic / imaging evidence of sacroiliitis and/or spinal inflammation * Patients must have daily spinal pain and stiffness for at least 2 weeks prior to randomization. This is defined by having a score of \>1 on questions #2 and #5 of the BASDAI score for the 2 weeks prior to randomization. * Patients receiving NSAIDS and/or COX-2 inhibitors must be on stable doses for at least 2 weeks prior to randomization. * Age \>18 years * Male and female patients, who are not surgically sterile or postmenopausal, must use reliable methods of birth control for the duration of the study. Males must agree to use barrier contraception for 3 months following the end of the trial. * Women of childbearing potential, not surgically sterile or postmenopausal, must have a negative serum beta HCG.
Exclusion criteria
* Use of DMARDs (methotrexate, d-penicillamine, sulfasalazine, azathioprine, hydroxychloroquine, or gold) within 8 weeks of randomization. * Use of systemic corticosteroids within 4 weeks of randomization * Use of intravenous or intra-articular corticosteroids within 4 weeks of randomization * Use of TNF alpha blockers (eg, infliximab, adalimumab) or etanercept as follows: Compound PK Exclusion period Etanercept T ½ = 102 hrs = 4.25 days 4 weeks Adalimumab T ½ 2 wks; 5 half lives 10 weeks 10 weeks Infliximab T ½ 7.7-9.5 d 12 weeks 8 weeks after maintenance dose median infx conc 0.5-6 mcg/ml * Therapy with an investigational agent within 30 days of randomization or 5 half-lives (pharmacokinetic or pharmacodynamic), which ever is longer * Known HIV or hepatitis B or C infection * Exclusion of tuberculosis (TB) * History of active Mycobacterium tuberculosis infection (any subspecies) within 3 years prior to the screening visit. Infections that occurred \> 3 years prior to entry must have been effectively treated. * History of incompletely treated latent Mycobacterium tuberculosis infection (as indicated by a positive Purified Protein Derivative \[PPD\] skin test) * Clinically significant abnormality on chest x-ray (CXR) if mantoux \>5mm or ELISPOT positive * History of other rheumatic autoimmune diseases (eg, systemic lupus erythematosus, rheumatoid arthritis, etc.) * Pregnant or nursing women * Any condition, in the investigator's opinion, which places the patient at an undue risk by participating in the study. * Contraindication to MRI and other MRI exclusions following local centre guidelines (Appendix H) * An estimated glomerular filtration rate (eGFR) of \< 60 ml/min (because of the small risk of nephrogenic sclerosing fibrosis with gadolinium intravenous contrast), if patient is to have MRI with gadolinium contrast . * Claustrophobia * Hemoglobin \< 9 g/dL * White blood cell (WBC) count \< 3000 /μL (≥ 3.0 X 109/L) and ≥ 14,000/μL (≥ 20 X 109/L) * Neutrophils \< 1500 /μL (\< 1.5 X 109/L) * Platelets \< 100,000 /μL (\< 100 X 109/L) * Serum creatinine \> 1.5 mg/dL (\> 132.6 μmol/L) * Total bilirubin \> 2.0 mg/dL * Aspartate transaminase (AST \[serum glutamic oxaloacetic transaminase, SGOT\]) and alanine transaminase (ALT \[serum glutamate pyruvic transaminase, SGPT\]) \> 1.5x upper limit of normal (ULN)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes of Apremilast in Patients With AS, Changes in BASDAI Score From Baseline | Baseline and 12 weeks | Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), 0 - 10 score, higher reduction in the scores suggest better suboptimal control of disease. |
| Changes of Apremilast on the Signs and Symptoms of AS, Night Pain From Baseline | Baseline and 12 weeks | This endpoint the night time pain score change was recorded by questionnaire to evaluate the Apremilast effect on symptom, higher reduction better improvement. scale is 0-10 |
| Effect of Apremilast in Patients With AS, Changes in BASFI Score | Baseline and 12 weeks | Bath Ankylosing Spondylitis Functional Index (BASFI), 0 - 10 score, higher reduction in the scores suggest better suboptimal control of disease. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Safety and Tolerability of Apremilast in AS, Number of Participants With Adverse Events | 16 weeks | To evaluate the safety and tolerability of Apremilast in AS, the investigator recorded the incidence of adverse events. |
Countries
United Kingdom
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Placebo placebo twice a day for 12 weeks, 4 weeks follow up
Placebo (sugar pill): twice a day | 19 |
| Apremilast 30 mg twice a day for 12 weeks, 4 weeks follow up
Apremilast: 10mg twice a day, dose was titrated by 20mg every 2 days until the maximum dose 30mg twice a day for 12weeks | 17 |
| Total | 36 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Treatment 12 Weeks | Adverse Event | 0 | 2 |
Baseline characteristics
| Characteristic | Placebo | Apremilast | Total |
|---|---|---|---|
| Age, Continuous | 39.21 years STANDARD_DEVIATION 13.3 | 44.88 years STANDARD_DEVIATION 11.1 | 42.95 years STANDARD_DEVIATION 11.01 |
| Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) | 4.36 units on a scale STANDARD_DEVIATION 1.75 | 4.79 units on a scale STANDARD_DEVIATION 2.16 | 4.57 units on a scale STANDARD_DEVIATION 1.95 |
| Bath Ankylosing Spondylitis Functional Index (BASFI) | 3.19 units on a scale STANDARD_DEVIATION 2.2 | 4.55 units on a scale STANDARD_DEVIATION 2.42 | 3.87 units on a scale STANDARD_DEVIATION 2.31 |
| CRP C-reactive protein | 6.24 mg/dl STANDARD_DEVIATION 2.56 | 11.37 mg/dl STANDARD_DEVIATION 12.12 | 8.8 mg/dl STANDARD_DEVIATION 7.34 |
| Race and Ethnicity Not Collected | — | — | 0 Participants |
| Region of Enrollment United Kingdom | 19 participants | 17 participants | 36 participants |
| Sex: Female, Male Female | 2 Participants | 2 Participants | 4 Participants |
| Sex: Female, Male Male | 17 Participants | 15 Participants | 32 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 19 | 0 / 19 |
| other Total, other adverse events | 17 / 19 | 18 / 19 |
| serious Total, serious adverse events | 0 / 19 | 0 / 19 |
Outcome results
Primary
Changes of Apremilast in Patients With AS, Changes in BASDAI Score From Baseline
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), 0 - 10 score, higher reduction in the scores suggest better suboptimal control of disease.
Time frame: Baseline and 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes of Apremilast in Patients With AS, Changes in BASDAI Score From Baseline | -0.77 units on a scale | Standard Deviation 1.47 |
| Apremilast | Changes of Apremilast in Patients With AS, Changes in BASDAI Score From Baseline | -1.59 units on a scale | Standard Deviation 1.48 |
p-value: 0.139ANCOVA
Primary
Changes of Apremilast on the Signs and Symptoms of AS, Night Pain From Baseline
This endpoint the night time pain score change was recorded by questionnaire to evaluate the Apremilast effect on symptom, higher reduction better improvement. scale is 0-10
Time frame: Baseline and 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Changes of Apremilast on the Signs and Symptoms of AS, Night Pain From Baseline | -0.23 score on a scale | Standard Deviation 2.75 |
| Apremilast | Changes of Apremilast on the Signs and Symptoms of AS, Night Pain From Baseline | -0.81 score on a scale | Standard Deviation 3.01 |
p-value: 0.58ANCOVA
Primary
Effect of Apremilast in Patients With AS, Changes in BASFI Score
Bath Ankylosing Spondylitis Functional Index (BASFI), 0 - 10 score, higher reduction in the scores suggest better suboptimal control of disease.
Time frame: Baseline and 12 weeks
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo | Effect of Apremilast in Patients With AS, Changes in BASFI Score | -0.28 units on a scale | Standard Deviation 1.61 |
| Apremilast | Effect of Apremilast in Patients With AS, Changes in BASFI Score | -1.74 units on a scale | Standard Deviation 1.91 |
p-value: 0.108ANCOVA
Secondary
The Safety and Tolerability of Apremilast in AS, Number of Participants With Adverse Events
To evaluate the safety and tolerability of Apremilast in AS, the investigator recorded the incidence of adverse events.
Time frame: 16 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Placebo | The Safety and Tolerability of Apremilast in AS, Number of Participants With Adverse Events | 17 Participants |
| Apremilast | The Safety and Tolerability of Apremilast in AS, Number of Participants With Adverse Events | 18 Participants |