cimzia

cimzia Uses, Dosage, Side Effects, Food Interaction and all others data.

cimzia is a pegylated monoclonal antibody against the tumor necrosis factor-alpha (TNF-alpha). It is formed with a humanized Fab fragment of 50 kDa, from an IgG 1 isotype, fused to a 40 kDa polyethylene glycol moiety replacing the Fc antibody region. The absence of the Fc region was ideated to prevent complement fixation and antibody-mediated cytotoxicity as well as to markedly increase its half-life.

Certolizumab does not require glycosylation for active function and hence, its production is significantly more affordable when compared to other existing TNF-alpha therapies as it can be done directly in bacterial hosts such as E. coli. It was developed and manufactured by UCB Pharma, first FDA approved in 2008 and updated for a new indication on March 28, 2019.

As part of the mechanism of action and nature of the drug, certolizumab does not induce apoptosis in cultured lymphocytes and monocytes. However, as a piece of the inhibition of inflammation, certolizumab pegol inhibits lipopolysaccharide-induced production of IL-1 beta and it induces nonapoptotic cell death via signaling transmembrane TNF-alpha.

cimzia
Uses
Dosage
Side Effect
Precautions
Interactions
Uses during Pregnancy
Uses during Breastfeeding
Accute Overdose
Food Interaction
Half Life
Volume of Distribution
Clearance
Interaction With other Medicine
Contradiction
Storage

Trade Name	cimzia
Generic	Certolizumab pegol
Certolizumab pegol Other Names	Certolizumab pegol
Weight	200mg, 200mg/ml,
Type	Injection, Solution, Subcutaneous Kit
Formula	C₂₁₁₅H₃₂₅₂N₅₅₆O₆₇₃S₁₆
Weight	91000.0 Da (Pegylated)
Protein binding	Monoclonal antibodies are usually not required to have protein binding studies.
Groups	Approved
Therapeutic Class
Manufacturer	U,c,b,, Ucb Pharma S,a, Ucb Pharma Limited
Available Country	Saudi Arabia, Australia, Canada, United Kingdom, United States, France, Netherlands, Portugal, Spain,
Last Updated:	September 19, 2023 at 7:00 am

Uses

cimzia is a tumor necrosis factor (TNF) blocker used to treat a variety of autoimmune and autoinflammatory conditions like Crohn's disease, rheumatoid arthritis, active psoriatic arthritis, ankylosing spondylitis, axial spondyloarthritis, and plaque psoriasis.

cimzia has been approved for several different conditions listed below:

Symptomatic management of Chron's disease patients and for the maintenance of clinical response in patients with moderate to severe disease with inadequate response to conventional therapy.
Treatment of adult patients with moderate to severely active rheumatoid arthritis.
Treatment of adult patients with active psoriatic arthritis.
Treatment of adult patients with active ankylosing spondylitis.
Treatment of adult patients with moderate-to-severe plaque psoriasis that are candidates for systemic therapy or phototherapy.
Treatment of adult patients with active non-radiographic axial spondyloarthritis with objective signs of inflammation.

In Canada, certolizumab pegol is additionally approved in combination with methotrexate for the symptomatic treatment, including major clinical response, and for the reduction of joint damage in adult patients with moderately to severely active rheumatoid arthritis and psoriatic arthritis.

Inflammation is a biological response against a potential threat. This response can be normal but in certain conditions, the immune system can attack the body's normal cells or tissues which causes an abnormal inflammation. TNF-alpha has been identified as a key regulator of the inflammatory response. The signaling cascades of this inflammatory mediator can produce a wide range of reactions including cell death, survival, differentiation, proliferation and migration.

cimzia is also used to associated treatment for these conditions: Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis, Moderate-to-severe Plaque Psoriasis, Moderately to Severely Active Rheumatoid Arthritis, Psoriatic Arthritis, Psoriatic arthritis aggravated, Severe Crohn's Disease, Active Ankylosing spondylitis, Moderate Crohn's disease, Moderate Rheumatoid arthritis, Severe Rheumatoid arthritis

How cimzia works

Certolizumab targets the activation of TNF-alpha with high affinity (KD 90 pM and IC90 0.004 mcg/ml) which in order, inhibits the downstream inflammatory process. It acts by binding and neutralizing the soluble and membrane portions of TNF-alpha without inducing complement or antibody-dependent cytotoxicity due to the lack of the Fc region. The inhibition of TNF-alpha is achieved in a dose-dependent manner and it does not present activity against lymphotoxin alpha (TNF-beta).

One additional feature od certolizumab pegol is that, due to the presence of the PEGylation, it is more significantly distributed into inflamed tissues when compared to other TNF-alpha inhibitors such as infliximab and adalimumab.

Toxicity

The oral ld50 observed in mice is determined to be of 300 mg/kg. To this date, there have not been reports of overdosage, however, in case of accidental overexposure close monitoring is recommended.

cimzia does not present mutagenic potential nor presents effects in fertility and reproductive performance. On the other hand, carcinogenicity studies have not been performed.

Volume of Distribution

cimzia volume of distribution is reported to be in the range of 4-8 L. It is known to have a very good distribution in the joints when compared to other TNF-alpha inhibitors.

Elimination Route

After subcutaneous administration, the peak plasma concentration is reached between 54 and 171 hours with a bioavailability of 80%. Certolizumab presents a linear pharmacokinetic profile with a peak plasma concentration of 43-49 mcg/ml.

Half Life

The circulatory half-life of certolizumab is of 14 days.

Clearance

The clearance rate of certolizumab pegol ranged between 9-14 ml/h when administered intravenously. However, when administered subcutaneously, the clearance rate is estimated to range between 14-21 ml/h depending on the patient condition.

Elimination Route

As certolizumab is a monoclonal antibody, the elimination route is not widely studied. However, it is known that the elimination of the PEG moiety is dependent on the renal function which links it directly with a high portion of renal elimination.