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Expert: PALOMA-3 Trial Results, Benefits of Subcutaneous Amivantamab for Lung Cancer Treatment

The PALOMA-3 trial showed subcutaneous amivantamab was better than IV for lung cancer patients.

United statesNatashab leighlKennedy ferruggiaPrincess margaret cancer centreAmerican society of clinical oncologyPharmacy timesMedical oncologistAmerican societyClinical oncology

Improved Outcomes With Subcutaneous Amivantamab in NSCLC

Subcutaneous amivantamab plus lazertinib may offer a survival benefit over intravenous administration, alongside dramatically reduced administration times, a new study suggests.

United statesJessicaj linNatashab leighlTreatment administration satisfaction questionnairePrincess margaret cancer centreCancer clinical research unitAmerican society of clinical oncologyHarvard medical schoolClinical oncologyMassachusetts general hospitalDrug administration

First results from late-breaking Phase 3 PALOMA-3 study show five-fold reduction in infusion-related reactions with five-minute subcutaneous amivantamab administration

New formulation showed non-inferiority to intravenous administration in fourth positive Phase 3 study in RYBREVANT® clinical program

United statesPrnewswire johnsonNatashab leighlNone of janssen research developmentJanssen research developmentJanssen biotech incPrincess margaret cancer centreAmerican society of clinical oncologyExchange commissionEuropean medicines agencyClinical oncologyAnnual meetingBiologics license applicationNew drug applicationPriority reviewPractice guidelines

Subcutaneous Amivantamab Plus Lazertinib Non-Inferior to IV Dosing in NSCLC

Unexpectedly offers a possible overall survival benefit, researchers say

United statesJessica jiyeong linMike bassettNatashab leighlPrincess margaret cancer centreHarvard medical schoolAmerican society of clinical oncologyAmerican societyClinical oncologyMassachusetts general hospital

First results from late-breaking Phase 3 PALOMA-3 study show five-fold reduction in infusion-related reactions with five-minute subcutaneous amivantamab administration

First results from late-breaking Phase 3 PALOMA-3 study show five-fold reduction in infusion-related reactions with five-minute subcutaneous amivantamab administration
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United statesNatashab leighlPrnewswire johnsonJanssen biotech incNone of janssen research developmentAmerican society of clinical oncology annual meetingEuropean medicines agencyAmerican lung associationNational cancer instituteWorld health organizationAmerican cancer societyAmerican society of clinical oncologyJanssen research developmentNational comprehensive cancer network incExchange commissionPrincess margaret cancer centre
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