Kelly Davio


Celltrion Receives Warning Letter From FDA

February 01, 2018

The FDA has issued a warning letter to Celltrion, maker of the infliximab biosimilar Inflectra. The company announced today that, on January 30, the company received a letter from the agency that “raises issues related to certain manufacturing process[es]” at its Incheon, Republic of Korea facility.

SB3 Shows Equivalence to Reference Trastuzumab in Phase 3 Study

January 31, 2018

A study newly published in the Journal of Clinical Oncology found that SB3, a proposed trastuzumab biosimilar being developed by Samsung Bioepis, demonstrated equivalence with European-sourced reference trastuzumab (Herceptin) in terms of breast pathologic complete response (bpCR) rate. Safety and immunogenicity for the 2 drugs were also similar.

Trump Says Drug Prices to "Come Rocketing Down" With Azar Helming HHS

January 30, 2018

Trump said of Azar, who was confirmed by a vote of 55 to 43 on January 24 to replace Tom Price, MD, as Secretary of HHS, “He’s going to get those prescription drug prices way down…it’s going to come rocketing down.”

Biosimilars Council Backs Pfizer With Amicus Brief in Ongoing Infliximab Case

January 30, 2018

On January 26, the Biosimilars Council (a division of the Association for Accessible Medicines) filed an amicus brief opposing Johnson & Johnson’s motion to dismiss a complaint brought by Pfizer over its biosimilar infliximab, Inflectra, which references Johnson & Johnson’s innovator product, Remicade.

Real-World Data Support the Noninferiority of Biosimilar Filgrastim in Preventing FN

January 26, 2018

Zarxio, a biosimilar filgrastim approved in the United States in 2015, was demonstrated to have no clinically meaningful differences from its reference in a randomized clinical trial setting, but data on its effectiveness in preventing febrile neutropenia (FN) a real-world setting have been limited thus far.

Treating Crohn Disease With Anti-TNF Drugs Reduces Mortality Rates

January 25, 2018

Although some studies have demonstrated an increased risk of death in patients with inflammatory bowel disease taking corticosteroids, the relationship between death and anti–tumor necrosis factor (anti-TNF) drugs has not been as clear.

EMA to Survey Pharma on Brexit Preparedness

January 24, 2018

The European Medicines Agency (EMA) has launched a survey of pharmaceutical companies to assess their preparedness for the United Kingdom’s upcoming withdrawal from the European Union, as it hopes to identify any concerns about the continued supply of drugs during the Brexit transition.

Report Points to Pricing, Litigation, and Lack of Interchangeability as Threats to Biosimilars

January 24, 2018

The report from Trinity Partners details findings from qualitative research with 10 medical directors at US payer organizations, representing plans covering over 100 million commercial and Medicare enrollees in the United States.