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large B-cell lymphoma

CHMP meeting highlights – June 2024

1 July 2024 | By Catherine Eckford (European Pharmaceutical Review)

In its latest meeting, the Committee for Medicinal Products for Human Use (CHMP) recommended several new medicines, including positive opinions for treatments for rare disorders.

news

Kite releases pivotal CAR T therapy Phase III study results

21 March 2023 | By Catherine Eckford (European Pharmaceutical Review)

Yescarta® is the first treatment in over 30 years to show statistically significant improvement in overall survival in R/R large B-cell lymphoma versus historical SOC.

news

FDA grants priority review of glofitamab for lymphoma

6 January 2023 | By Catherine Eckford (European Pharmaceutical Review)

Glofitamab for relapsed or refractory large B-cell lymphoma has been granted priority review by the US Food and Drug Administration (FDA).

news

FDA priority review for AbbVie lymphoma bispecific antibody

22 November 2022 | By Catherine Eckford (European Pharmaceutical Review)

The FDA has accepted priority review of epcoritamab for adults with relapsed/refractory large B-cell lymphoma, which could be the first subcutaneous bispecific antibody for large B-cell lymphoma.

podcasts

EPR Podcast Episode 16 – Evolving QC for Cell & Gene Therapy – Félix Montero Julian and Thomas Jones, bioMérieux

1 November 2022 | By European Pharmaceutical Review

What’s new in the cell and gene therapy landscape? What is the role of quality control in efforts to scale up manufacturing of CGT products and alleviate talent constraints? Find out more in this podcast with bioMérieux…

news

EMA validates AbbVie lymphoma bispecific antibody application

31 October 2022 | By Catherine Eckford (European Pharmaceutical Review)

AbbVie's marketing application for epcoritamab in adults with relapsed/refractory diffuse large B-cell lymphoma has been validated by the European Medicines Agency.

news

Merck to acquire VelosBio for $2.75 billion

10 November 2020 | By Hannah Balfour (European Pharmaceutical Review)

The acquisition will strengthen Merck’s oncology pipeline with VLS-101, an investigational antibody-drug conjugate in trials for haematological malignancies and solid tumours.

news

EMA announces medicine approval recommendations from November meeting

18 November 2019 | By Victoria Rees (European Pharmaceutical Review)

The EMA CHMP has revealed its suggestion to grant marketing authorisation to seven medicines after its most recent meeting.

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large B-cell lymphoma