Tezepelumab

Hypersensitivity. Concomitant use with live attenuated vaccine.

Patient with known parasitic (helminth) infection. Not indicated for the treatment of acute asthma symptoms or acute exacerbations, including status asthmaticus. Children. Pregnancy and lactation.

Significant: Hypersensitivity reactions (e.g. anaphylaxis, allergic conjunctivitis, rash); risk of serious infections; serious cardiac events.
General disorders and administration site conditions: Local inj site reactions (e.g. erythema, pain, swelling).
Immune system disorders: Antibody development.
Infections and infestations: Pharyngitis.
Musculoskeletal and connective tissue disorders: Back pain, arthralgia.

SC: Z (Avoid unless benefits outweigh risks. Consult product literature for specific recommendations.)

Monitor forced expiratory volume in the 1st second (FEV₁), peak flow, other pulmonary function tests. Monitor for signs and symptoms of hypersensitivity reactions, infections, uncontrolled or worsening asthma conditions, and cardiac events (e.g. dyspnoea, chest pain, feeling of fainting or being lightheaded, malaise).

May enhance the adverse effects of live vaccines.

Description:
Mechanism of Action: Tezepelumab is a recombinant human monoclonal antibody IgG₂ lambda. Its exact mechanism of action has not been fully established, but it is known to bind to human thymic stromal lymphopoietin (TSLP), preventing its interaction with heterodimeric TSLP receptor. TSLP inhibition leads to the reduction of inflammatory biomarkers and cytokines associated with airway inflammation (e.g. airway submucosal eosinophils, blood eosinophils, IgE, fraction of expired nitric oxide (FeNO), interleukin (IL)-5, and IL-13).
Onset: Approx 2 weeks.
Pharmacokinetics:
Absorption: Bioavailability: Approx 77%. Time to peak plasma concentration: Approx 3-10 days.
Distribution: Crosses the placenta. Volume of distribution: 3.9 L (central); 2.2 L (peripheral).
Metabolism: Metabolised via proteolytic degradation by enzymes widely distributed in the body.
Excretion: Via intracellular catabolism. Elimination half-life: Approx 26 days.

Store between 2-8°C. Do not freeze. Do not shake. May be stored between 20-25°C for up to 30 days; discard if unused after 30 days. Do not put back in the refrigerator. Protect from light. Do not expose to heat.

Thuốc trị hen & bệnh phổi tắc nghẽn mạn tính

R03DX11 - tezepelumab ; Belongs to the class of other systemic drugs used in the treatment of obstructive airway diseases.

Anon. Tezepelumab. AHFS Clinical Drug Information [online]. Bethesda, MD. American Society of Health-System Pharmacists, Inc. https://www.ahfscdi.com. Accessed 01/04/2024.

Buckingham R (ed). Tezepelumab. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 01/04/2024.

Joint Formulary Committee. Tezepelumab. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 01/04/2024.

Paediatric Formulary Committee. Tezepelumab. BNF for Children [online]. London. BMJ Group, Pharmaceutical Press, and RCPCH Publications. https://www.medicinescomplete.com. Accessed 01/04/2024.

Tezepelumab. Gold Standard Drug Database in ClinicalKey [online]. Elsevier Inc. https://www.clinicalkey.com. Accessed 01/04/2024.

Tezepelumab. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 01/04/2024.

Tezspire 210 mg Solution for Injection in Pre-filled Syringe (AstraZeneca UK Limited). MHRA. https://products.mhra.gov.uk. Accessed 01/04/2024.

Tezspire 210 mg Solution for Injection in Pre-filled Syringe or Pen (AstraZeneca AB). MIMS Singapore. http://www.mims.com/singapore. Accessed 01/04/2024.

Tezspire Injection, Solution (Amgen, Inc). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 01/04/2024.