MedPath

Canakinumab

Generic Name
Canakinumab
Brand Names
Ilaris
Drug Type
Biotech
Chemical Formula
-
CAS Number
914613-48-2
Unique Ingredient Identifier
37CQ2C7X93
Background

Canakinumab is a recombinant, human anti-human-IL-1β monoclonal antibody that belongs to the IgG1/κ isotype subclass. It is expressed in a murine Sp2/0-Ag14 cell line and comprised of two 447- (or 448-) residue heavy chains and two 214-residue light chains, with a molecular mass of 145157 Daltons when deglycosylated. Both heavy chains of canakinumab contain oligosaccharide chains linked to the protein backbone at asparagine 298 (Asn 298). Canakinumab binds to human IL-1β and neutralizes its inflammatory activity by blocking its interaction with IL-1 receptors, but it does not bind IL-1alpha or IL-1 receptor antagonist (IL-1ra). Canakinumab is marketed under the brand name Ilaris and indicated for patients 4 years of age and older to treat Familial Cold Autoinflammatory Syndrome (FCAS) and Muckle-Wells Syndrome (MWS), which are both part of the Cryopyrin-Associated Periodic Syndromes (CAPS) as well as for patients 2 years of age and older to treat systemic juvenile idiopathic arthritis (SJIA). Clinical trials have established the administration of canakinumab every 2 weeks to be safe and effective, offering a considerable advantage over the existing treatment with the human IL-1 receptor antagonist, anakinra, which must be injected daily and which is often poorly tolerated by patients.

Indication

Canakinumab is indicated for the treatment of periodic fever syndromes in specific patient populations. In patients ≥4 years of age, canakinumab is indicated for the treatment of Cryopyrin-Associated Periodic Syndromes (CAPS), including Familial Cold Auto-inflammatory Syndrome (FCAS) and Muckle-Wells Syndrome (MWS). In adult and pediatric patients, canakinumab is also indicated for the treatment of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS), Hyperimmunoglobulin D Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD), and Familial Mediterranean Fever (FMF).

Canakinumab is additionally indicated in patients ≥2 years of age for the treatment of active Still's disease, including Adult-Onset Still's Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA).

Canakinumab is also indicated for the treatment of gout flares in adult patients in whom standard therapies (e.g. NSAIDs, colchicine) are contraindicated, not tolerated, or ineffective, and in whom repeated courses of corticosteroids are not appropriate.

Associated Conditions
Adult Onset Still's Disease, Cryopyrin-associated Periodic Syndromes (CAPS), Familial Cold Autoinflammatory Syndrome (FCAS), Familial Mediterranean Fever (FMF ), Gout Flares, Mevalonate Kinase Deficiency, Muckle-Wells Syndrome (MWS), Systemic Juvenile Idiopathic Arthritis (SJIA), Tumour necrosis factor receptor-associated periodic syndrome
Associated Therapies
-

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ACZ885 in Patients With Type 2 Diabetes

Phase 2
Completed
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2008-01-31
Last Posted Date
2012-02-13
Lead Sponsor
Novartis
Target Recruit Count
231
Registration Number
NCT00605475
Locations
🇺🇸

Allied Research International - Cetero Research Miami, Miami, Florida, United States

🇺🇸

Elite Research Institute Miami, Miami, Florida, United States

🇷🇺

Novartis Investigative Site, St. Petersberg, Russian Federation

and more 5 locations

Safety and Efficacy of Multiple Doses of Canakinumab (ACZ885) in Chronic Obstructive Pulmonary Disease (COPD) Patients

Phase 1
Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Placebo
Drug: Canakinumab
First Posted Date
2007-12-28
Last Posted Date
2011-06-30
Lead Sponsor
Novartis
Target Recruit Count
147
Registration Number
NCT00581945
Locations
🇺🇸

Novartis Investigator Site, Richmond, Virginia, United States

Long-term Efficacy, Safety and Tolerability of ACZ885 in Patients With Rheumatoid Arthritis

Phase 2
Completed
Conditions
Rheumatoid Arthritis
Interventions
First Posted Date
2007-11-07
Last Posted Date
2021-07-09
Lead Sponsor
Novartis
Target Recruit Count
115
Registration Number
NCT00554606
Locations
🇹🇷

Novartis Investigator Site, Sihhiye/Ankara, Turkey

Efficacy and Safety of Subcutaneous Versus Intravenous ACZ885 in Adult Patients With Established Rheumatoid Arthritis

Phase 1
Terminated
Conditions
Rheumatoid Arthritis
Interventions
First Posted Date
2007-07-20
Last Posted Date
2009-08-25
Lead Sponsor
Novartis
Target Recruit Count
11
Registration Number
NCT00505089
Locations
🇵🇱

Novartis Investigative Site, Grodzisk Mazowiecki, Poland

🇳🇱

Novartis investigative site, Leiden, Netherlands

🇵🇱

Novartis Investigator Site, Poznan, Poland

and more 1 locations

Safety and Tolerability of an Intravenous Infusion of ACZ885 in Patients With Wet Age-Related Macular Degeneration

Phase 1
Completed
Conditions
Wet Age-Related Macular Degeneration
First Posted Date
2007-07-18
Last Posted Date
2007-12-28
Lead Sponsor
Novartis
Target Recruit Count
20
Registration Number
NCT00503022

Safety, Efficacy, Pharmacokinetics, Pharmacodynamics of ACZ885 in Patients With NALP3 Mutations and Clinical Symptoms

Phase 2
Completed
Conditions
NALP3 Mutation
Interventions
First Posted Date
2007-06-19
Last Posted Date
2009-02-17
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
34
Registration Number
NCT00487708
Locations
🇩🇪

Novartis investigative site, Nuernberg, Germany

🇪🇸

Novartis Investigator Site, Oviedo, Spain

🇬🇧

Novartis Investigative site, London, United Kingdom

Efficacy, Safety, and Tolerability of ACZ885 in Patients With Muckle-Wells Syndrome

Phase 3
Completed
Conditions
Muckle Wells Syndrome
Interventions
Drug: Placebo
Drug: ACZ885
First Posted Date
2007-04-27
Last Posted Date
2017-08-28
Lead Sponsor
Novartis
Target Recruit Count
35
Registration Number
NCT00465985
Locations
🇫🇷

Novartis Investigational Site, Lille Cedex, France

🇬🇧

Novartis Investigative Site, London, United Kingdom

Safety, Efficacy and Pharmacokinetics of Subcutaneous ACZ885 in Patients With Systemic Juvenile Idiopathic Arthritis (SJIA)

Phase 1
Completed
Conditions
Arthritis, Juvenile Rheumatoid
Interventions
First Posted Date
2007-01-24
Last Posted Date
2011-08-09
Lead Sponsor
Novartis
Target Recruit Count
26
Registration Number
NCT00426218
Locations
🇮🇹

Novartis Investigative site, Origgio, Italy

Efficacy, Safety and Tolerability of ACZ885 in Patients With Active Rheumatoid Arthritis

Phase 2
Completed
Conditions
Rheumatoid Arthritis
Interventions
Drug: Canakinumab
Drug: Placebo
First Posted Date
2007-01-19
Last Posted Date
2014-02-10
Lead Sponsor
Novartis
Target Recruit Count
274
Registration Number
NCT00424346
Locations
🇪🇸

Novartis, Barcelona, Spain

🇺🇸

Sun Valley Arthritis Center, Ltd, Peoria, Arizona, United States

🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

and more 10 locations

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ACZ885 in Healthy Japanese Male Volunteers

Phase 1
Completed
Conditions
Healthy
First Posted Date
2007-01-11
Last Posted Date
2012-04-30
Lead Sponsor
Novartis
Target Recruit Count
48
Registration Number
NCT00421226
Locations
🇯🇵

Novartis Investigative site, Tokyo, Japan

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