CHMP recommends EU approval of Roche’s subcutaneous formulation of Lunsumio for people with relapsed or refractory follicular lymphoma

Roche

19 September 2025 - Subcutaneous Lunsumio has potential to substantially reduce treatment administration time with an approximately one minute injection, compared with 2-4 hours intravenous infusion.

Roche announced today that the EMA’s CHMP has recommended the approval of a subcutaneous formulation of Lunsumio (mosunetuzumab) for the treatment of adult patients with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy.

Read Roche press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Registration