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A safer treatment path for high-risk children to overcome food allergies - Vimarsana News

A safer treatment path for high-risk children to overcome food allergies

New UBC research reveals a safe path to overcoming food allergies for older children and others who can’t risk consuming allergens orally to build up their resistance.

CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed - Vimarsana News

CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed

CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy Expanded indication for this one-time infusion may provide pati...

Johnson & Johnson : CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy - Vimarsana News

Johnson & Johnson : CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy

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J&J: EU green light for Carvykti in multiple myeloma - Vimarsana News

J&J: EU green light for Carvykti in multiple myeloma

Janssen-Cilag International NV, a Johnson & Johnson company, announced today that the European Commission has approved a type II variant for Carvykti . This latest approval is for the treatment of...

European Commission Approves Cilta-Cel for Relapsed/Refractory Multiple Myeloma - Vimarsana News

European Commission Approves Cilta-Cel for Relapsed/Refractory Multiple Myeloma

Cilta-cel has received approval from the European Commission for multiple myeloma that is relapsed or refractory to at least 1 prior line of therapy.