The Center for Biosimilars Staff


Theradiag Partners with Biogaran on Infliximab Biosimilar Monitoring Kits in France

March 31, 2018

Last week, Theradiag, a French company specializing in in vitro diagnostics and theranostics (targeted therapy based on findings in diagnostic tests) announced that it has entered a new partnership agreement with pharmaceutical group Biogaran.

European Competition for Trastuzumab to Heat Up as ABP 980 Gains Positive CHMP Opinion

March 25, 2018

Amgen and its partner Allergan announced Friday that their ABP 980, a trastuzumab biosimilar referencing Herceptin, has gained a positive opinion for marketing from the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP).

No Negative Impact on Quality of Life With Subcutaneous Trastuzumab

March 14, 2018

Patients without comorbidities who received subcutaneous trastuzumab with their chemotherapy and endocrine therapy showed a significant improvement in emotional function, and reported that they were less upset by hair loss than the patients in the control group.

IQVIA Report Predicts the "Next Large Wave of Biosimilars"

March 13, 2018

The IQVIA Institute for Human Data Science (formerly the IMS institute) has released a new report making predictions for the healthcare landscape in 2018 and beyond, and the report’s authors see biosimilars as having a key role in developed markets in the years ahead.

European Commission Issues 8th Report on Drug Patent Settlements

March 12, 2018

The number of patent settlements that limit generic drugs' market entry and involve a transfer of value (monetary or otherwise) for the delay of entry have stabilized at a low level, says the European Commission.

United Kingdom Should Remain an EMA Member, Says Theresa May

March 06, 2018

On March 2, UK Prime Minister Theresa May delivered a speech on the future of the United Kingdom’s relationship with the European Union, calling for the United Kingdom to remain a member of the European Medicines Agency (EMA), and saying that the United Kingdom could commit to abiding by the rules of the EMA and “making an appropriate financial contribution” to the agency.