Acute Gout
Conditions
Brief summary
The purpose of this study is to determine the efficacy and safety of recombinant anti-IL-1β humanized monoclonal antibody injection in Chinese participants with acute gout.
Detailed description
Study SSGJ-613-AG-III-01 is a phase 3, multicenter, randomized, double-blind, double-dummy, active-controlled, parallel-group study examining the effect of recombinant anti-IL-1β humanized monoclonal antibody injection versus compound betamethasone injection in Chinese adult patients with frequent flares of acute gouty arthritis who are contraindicated, intolerant, or lack efficacy to non-steroidal anti-inflammatory drugs (NSAIDs) and/or colchicine. The entire treatment period is 48 weeks, consisting of a double-blind treatment period of 24 weeks and an open treatment period of 24 weeks.
Interventions
one s.c. injection of SSGJ-613 once, on Day 1.
OTHERPlacebo
Participants will receive Placebo matching Compound Betamethasone Injection to maintain the blinding of the Investigational Medicinal Products.
1 mL i.m. once on Day 1
Sponsors
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
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 75 Years
Healthy volunteers
No
Inclusion criteria
* Must be 18 Years to 75 Years, both male and female. * BMI ≤35 kg/m2. * Meeting the American College of Rheumatology (ACR) 2015 criteria for the classification of acute arthritis of primary gout. * History of ≥ 3 gout flares within the 12 months prior to study randomization. * Onset of current acute gout flare within 4 days prior to study screening. * Screening pain intensity of the Target Joint ≥ 50 mm on the 0-100 mm VAS. * Contraindicated, intolerant or lack efficacy to NSAIDs and/or colchicine. * Accept uric acid lowering treatment according to the requirements of the protocol.
Exclusion criteria
* Gout caused by radiotherapy/chemotherapy, lead, organ transplantation, tumors, etc. * Evidence/suspicion of infectious/septic arthritis, or other acute inflammatory arthritis. * Presence of severe renal function impairment. * Intolerance of subcutaneous and intramuscular injection. * Known presence or suspicion of active or recurrent bacterial, fungal or viral infection at the time of enrollment. * History of malignant tumor within 5 years before screening. * Live vaccinations within 8 weeks prior to the start of the study. * Use of forbidden therapy.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The Change in Pain Intensity in the Target Joint From Baseline to 72 Hours Post Dose as Measured on a 0-100 mm Visual Analog Scale (VAS) | 72 hours post-dose | The change in pain intensity from baseline to 72 hours post dose as measured on a 0-100 mm Visual Analog Scale (VAS): 0= no pain and 100= severe pain. Change from baseline = (post-baseline measurement - baseline). |
| Time to First New Flare | 12 weeks | The Kaplan Meier method was used to estimate the median time and 95% CI of the first new flares within 12 weeks after the first administration of each group, as well as the event incidence and 95% CI at 12 weeks. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Time to Complete Pain Remission of Baseline Pain Intensity in the Target Joint after study drug administration | Up to 48 weeks | The time to complete pain remission in Pain intensity from baseline as measured by a 5-point Likert scale for each treatment group, is estimated using the Kaplan Meier method. Participants scored their pain intensity in the target joint on a 5-point Likert scale: None, mild, moderate, severe, extremely severe. |
| Percentage of Participants with Complete Pain Remission of the Target Joint within 12 weeks after study drug administration | 12 weeks | Participants scored their pain intensity in the target joint on a 5-point Likert scale: None, mild, moderate, severe, extremely severe. |
| Time to first use of Rescue Medication | Within 7 days after the first administration, within 7 days after the last acute attack of gout during the double blind treatment period | The Kaplan Meier method was used to estimate the median time and 95% CI of the first use of Rescue Medication. |
| Percentage of Participants Taking Rescue Medication After Study Drug Administration and Categories and Dosages of Rescue Medication | 12 weeks, 24 weeks, 48 weeks | — |
| The Change in Pain Intensity in the Target Joint From Baseline to 6, 24, 48 Hours and 7 Days Post Dose as Measured on a 0-100 mm Visual Analog Scale (VAS) | At 6, 24, 48 hours and 7 Days post-dose | The change in pain intensity from baseline to 6, 12, 48 hours and 7 days post dose as measured on a 0-100 mm Visual Analog Scale (VAS): 0= no pain and 100= severe pain. Change from baseline = (post-baseline measurement - baseline). |
| Time to First New Flare | 24 weeks, 48 weeks | The Kaplan Meier method was used to estimate the median time and 95% CI of the first new flares after the first administration of each group, as well as the event incidence and 95% CI. |
| Percentage of Participants with at least 1 new gout flare | 12 weeks, 24 weeks, 48 weeks | — |
| Number of new gout flares | 12 weeks, 24 weeks, 48 weeks | — |
| Likert scores for target joint pain | 7 days, 12 weeks, 24 weeks | Patients scored their pain intensity on a 5-point Likert scale (none, mild, moderate, severe, extreme). |
| The Time to At Least 50% Reduction of Baseline Pain Intensity in the Target Joint after study drug administration | Up to 48 weeks | The time to at least 50% reduction in Pain intensity from baseline as measured by Visual Analog Scale (VAS) for each treatment group, is estimated using the Kaplan Meier method. Participants scored their pain intensity in the target joint on a 0-100 mm VAS, ranging from no pain (0) to unbearable pain (100). |
Contacts
Primary ContactQinghong Zhou, MD
Outcome results
None listed