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bevacizumab

Acquisition deal to back European biosimilars market

30 November 2023 | By Catherine Eckford (European Pharmaceutical Review)

Following the acquisition from Viatris, Biocon Biologics and its partners state that they will commercialise biosimilar products in 31 European countries.

news

Clinical trial-first for liver cancer immunotherapy combo

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

IMbrave050 is the first Phase III study to show a cancer immunotherapy combo reduced risk of disease recurrence for early-stage hepatocellular carcinoma.

news

EMA’s human medicines committee (CHMP) Feb meeting highlights

28 February 2022 | By European Pharmaceutical Review

Highlights of the February 2022 meeting of EMA’s human medicines committee (CHMP) include the recommendation of 13 medicines for approval, along with updates to other drugs and COVID-19 vaccines.

article

Merck’s Keytruda^®: update on trials and outcomes

8 October 2021 | By Anna Begley (European Pharmaceutical Review)

EPR’s Anna Begley summarises some of the key results from trials of Merck’s Keytruda® (pembrolizumab) cancer treatment.

news

Biologics patent expiry to positively impact US pharma, says report

11 February 2020 | By Victoria Rees (European Pharmaceutical Review)

New research has suggested that the expiration of biologics patents will be the factor that positively impacts US pharma the most this year.

news

FDA antibody biosimilar product approvals increase in 2019

9 August 2019 | By European Pharmaceutical Review

2019 has seen a marked increase of antibody biosimilar product approvals in the first half of the year, according to a report.

news

Arfolitixorin linked to tumour shrinkage in colorectal cancer

18 January 2019 | By European Pharmaceutical Review

A Phase I/IIa study has shown that arfolitixorin along with either irinotecan or oxaliplatin could shrink the size of tumours in colorectal cancer patients...

news

Study reveals huge improvement for severe HHT patients after bevacizumab treatment

31 January 2018 | By European Pharmaceutical Review

A new study reveals the efficacy and safety of using intravenous bevacizumab to treat patients with severe hereditary haemorrhagic telangiectasia (HHT). Successful results suggest it should be used as a first-line therapy.

news

EC approves first biosimilar Mvasi for the treatment of cancer

19 January 2018 | By Dr Zara Kassam (European Pharmaceutical Review)

The European Commission has granted marketing authorisation for Mvasi for the treatment of certain types of cancer...

news

BIOCAD does its sums for growth

28 July 2017 | By Steve Bremer (European Pharmaceutical Review)

Russian biotech company BIOCAD plans to leverage competitive advantages to take 5% of the European medicines market

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