Retsevmo (selpercatinib)

CHMP meeting highlights: January 2024

30 January 2024 | By Catherine Eckford (European Pharmaceutical Review)

In its first meeting of 2024, the CHMP recommended a generic medicine for schizophrenia and refused a marketing authorisation (MA) for geographic atrophy.

news

UK conditionally approves Lilly’s Retsevmo^® for RET-driven lung and thyroid cancers

12 March 2021 | By Hannah Balfour (European Pharmaceutical Review)

The conditional marketing authorisation of Retsevmo® (selpercatinib) was based on positive results from the LIBRETTO-001 Phase I/II trial.

news

EMA recommends 15 medicines for approval following December meeting

14 December 2020 | By Victoria Rees (European Pharmaceutical Review)

The EMA's human medicines committee has released its results for the December meeting, suggesting which therapies should receive marketing authorisation.

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Recommended

Retsevmo (selpercatinib)

CHMP meeting highlights: January 2024

UK conditionally approves Lilly’s Retsevmo® for RET-driven lung and thyroid cancers

EMA recommends 15 medicines for approval following December meeting

UK conditionally approves Lilly’s Retsevmo^® for RET-driven lung and thyroid cancers