Amivantamab 350mg/7mL (50mg/mL) Injection

Amivantamab 350mg/7mL (50mg/mL) is a targeted antibody treatment for selected advanced non-small cell lung cancers with EGFR alterations. Treatment selection depends on tumour testing and the combination regimen being used.
It is diluted and given by intravenous infusion. The first dose is divided across two days, with premedication and careful observation for infusion-related reactions.
The antibody binds EGFR and MET receptors, blocks growth signalling and helps immune cells identify and destroy tumour cells.
Rash, nail inflammation, mouth sores, swelling and tiredness can occur. Infusion reactions and inflammation of the lungs are important risks.
Report new breathlessness or a worsening cough promptly. Sun protection and early skin and nail care help manage treatment-related skin problems.
Targets receptor pathways driving susceptible lung cancers and can improve disease control in a molecularly selected population.
The result establishes whether the cancer has an EGFR alteration for which the treatment regimen is appropriate.
Splitting the initial dose and using premedication helps manage the high first-infusion reaction risk.
Yes. EGFR is also present in normal skin, so blocking it can produce rash and nail-fold inflammation.
It is a targeted antibody. Some regimens combine it with chemotherapy or another targeted treatment.
EGFR: a receptor that can drive tumour growth. MET: another growth-signalling receptor. NSCLC: non-small cell lung cancer.; AR: Amivantamab 350mg/7mL (50mg/mL) حقن; FR: Amivantamab 350mg/7mL (50mg/mL) injection; PT: Amivantamab 350mg/7mL (50mg/mL) injeção; ES: Amivantamab 350mg/7mL (50mg/mL) inyección; RU: Amivantamab 350mg/7mL (50mg/mL) инъекция; ID: Amivantamab 350mg/7mL (50mg/mL) suntikan; VI: Amivantamab 350mg/7mL (50mg/mL) thuốc tiêm; MS: Amivantamab 350mg/7mL (50mg/mL) suntikan; TL: Amivantamab 350mg/7mL (50mg/mL) iniksyon; ZH-SG: Amivantamab 350mg/7mL (50mg/mL) 注射剂
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Amivantamab 350mg/7mL (50mg/mL) Injection