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
-

A Phase IB Study to Determine the Safety and Tolerability of Canakinumab and Tislelizumab in Combination With Nab-Paclitaxel and Gemcitabine in the Neo-adjuvant Treatment of Patients With Pancreatic Cancer

Phase 1
Recruiting
Conditions
Pancreatic Cancer
Interventions
First Posted Date
2023-08-09
Last Posted Date
2024-06-26
Lead Sponsor
NYU Langone Health
Target Recruit Count
10
Registration Number
NCT05984602
Locations
🇺🇸

NYU Langone Ambulatory Care Center East 38th Street, New York, New York, United States

🇺🇸

Ambulatory Care Center, New York, New York, United States

🇺🇸

Clinical Cancer Center, New York, New York, United States

A Prevention Trial of Canakinumab in Subjects at High Risk for Lung Cancer

Phase 3
Terminated
Conditions
Lung Cancer
Interventions
Drug: Placebo
Drug: Canakinumab
First Posted Date
2023-02-13
Last Posted Date
2023-02-13
Lead Sponsor
Mario Negri Institute for Pharmacological Research
Target Recruit Count
350
Registration Number
NCT05725343
Locations
🇮🇹

Ente Ospedaliero Ospedali Galliera, Genova, Italy

🇮🇹

Ospedale San Martino, Genova, Italy

🇮🇹

IRST Meldola, Meldola, Italy

and more 3 locations

Canakinumab for the Prevention of Progression to Cancer in Patients With Clonal Cytopenias of Unknown Significance, IMPACT Study

Phase 2
Recruiting
Conditions
Clonal Cytopenia of Undetermined Significance
Interventions
Procedure: Biospecimen Collection
Procedure: Bone Marrow Aspiration and Biopsy
Procedure: Chest Radiography
Drug: Canakinumab
Procedure: Echocardiography
Drug: Placebo Administration
Other: Quality-of-Life Assessment
First Posted Date
2022-12-08
Last Posted Date
2024-12-20
Lead Sponsor
Uma Borate
Target Recruit Count
110
Registration Number
NCT05641831
Locations
🇺🇸

Weill Cornell Medical College, New York, New York, United States

🇺🇸

Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States

🇺🇸

Vanderbilt University Medical Center, Nashville, Tennessee, United States

and more 1 locations

Using a Contact Dermatitis Model With Biologic Medications to Study Skin Inflammation

Phase 2
Recruiting
Conditions
Skin Inflammation
Allergic Contact Dermatitis
Interventions
First Posted Date
2022-09-10
Last Posted Date
2024-05-23
Lead Sponsor
John Harris
Target Recruit Count
45
Registration Number
NCT05535738
Locations
🇺🇸

University of Massachusetts Chan Medical School, Worcester, Massachusetts, United States

Study of Canakinumab in Patients With Myelofibrosis

Phase 2
Active, not recruiting
Conditions
Primary Myelofibrosis
Post-essential Thrombocythemia Myelofibrosis
PV-MF
ET-MF
Post-polycythemia Vera Related Myelofibrosis
Interventions
First Posted Date
2022-07-21
Last Posted Date
2024-11-28
Lead Sponsor
John Mascarenhas
Target Recruit Count
10
Registration Number
NCT05467800
Locations
🇺🇸

Mayo Clinic Arizona, Phoenix, Arizona, United States

🇺🇸

Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California, United States

🇺🇸

Moffitt Cancer Center, Tampa, Florida, United States

and more 4 locations

Canakinumab for the Treatment of Postprandial Hypoglycemia

Phase 3
Recruiting
Conditions
Postprandial Hypoglycemia
Interventions
Drug: Placebo (0.9% NaCl)
Drug: Canakinumab
First Posted Date
2022-06-02
Last Posted Date
2024-07-03
Lead Sponsor
University Hospital, Basel, Switzerland
Target Recruit Count
56
Registration Number
NCT05401578
Locations
🇨🇭

University Hospital Basel, Division of Endocrinology, Diabetes and Metabolism, Basel, Switzerland

🇨🇭

Cantonal Hospital Olten, Division of Endocrinology, Olten, Switzerland

A Study of Canakinumab With Chemotherapy, Radiation Therapy, and Durvalumab in People With Lung Cancer

Phase 2
Active, not recruiting
Conditions
Non-small Cell Lung Cancer
Interventions
Drug: Canakinumab
Drug: Durvalumab
Radiation: Radiation therapy
Drug: Chemotherapy
First Posted Date
2021-05-27
Last Posted Date
2024-06-18
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Target Recruit Count
41
Registration Number
NCT04905316
Locations
🇺🇸

Memorial Sloan Kettering Commack, Commack, New York, United States

🇺🇸

Memorial Sloan Kettering Nassau, Uniondale, New York, United States

🇺🇸

Memorial Sloan Kettering Cancer Center, New York, New York, United States

and more 4 locations

Phase Ib Study of Select Drug Combinations in Patients With Lower Risk MDS

Phase 1
Terminated
Conditions
Myelodysplastic Syndromes
Interventions
Drug: canakinumab
Drug: MBG453
Drug: NIS793
First Posted Date
2021-03-23
Last Posted Date
2024-05-17
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
33
Registration Number
NCT04810611
Locations
🇺🇸

The Ohio State University Wexner Medical Center ., Columbus, Ohio, United States

🇺🇸

Massachusetts General Hospital ., Boston, Massachusetts, United States

🇺🇸

City Of Hope National Med Center Oncology, Duarte, California, United States

and more 3 locations

Canakinumab With Darbepoetin Alfa in PTs With Lower-Risk MDS Who Have Failed ESA

Phase 1
Recruiting
Conditions
Myelodysplastic Syndromes
Interventions
First Posted Date
2021-03-15
Last Posted Date
2025-01-09
Lead Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Target Recruit Count
41
Registration Number
NCT04798339
Locations
🇺🇸

Moffitt Cancer Center, Tampa, Florida, United States

🇺🇸

Emory-Winship Cancer Institute, Atlanta, Georgia, United States

Study of the Efficacy and Safety of Various Anti-inflammatory Agents in Participants With Mild Cognitive Impairment or Mild Alzheimer's Disease

Phase 2
Terminated
Conditions
Mild Cognitive Impairment
Alzheimer Disease
Interventions
First Posted Date
2021-03-12
Last Posted Date
2024-12-27
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
34
Registration Number
NCT04795466
Locations
🇺🇸

Massachusetts General Hospital, Charlestown, Massachusetts, United States

🇺🇸

SUNY at Stony Brook, Stony Brook, New York, United States

🇬🇧

Novartis Investigative Site, Southampton, United Kingdom

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