Biosimilars

Top news of the day from across the health care landscape.

Another state passes legislation to increase uptake of biosimilars.

Jonathan Van Lare, PharmD, director of Pharmacy Advantage, discusses the growth of biosimilars in specialty pharmacy.

The World Health Organization recently announced plans to launch a pilot program for prequalifying biosimilars.

World Health Organization plans to launch a biosimilar prequalification program.

FDA authorizes an omalizumab (Xolair) biosimilar to commence clinical trials.

GBR 310 is a recombinant DNA-derived monoclonal antibody for the treatment of allergic asthma and chronic idiopathic urticaria.

Increased development of biosimilars will drive the need for analytical instrument analyzers, report finds.

Suzette DiMascio, CHE, CMCE, CPC, president and CEO of CSI Specialty Group, discusses the potential impact of biosimilars on specialty pharmacy.

Amgen is claiming patent infringement against Sanofi and Regeneron based on the biological mechanisms of dupilumab (Dupixent).

Litigation to continue surrounding biological mechanisms of dupilumab (Dupixent).

Amgen’s 2017 Trends in Biosimilars report examines commercialization and distribution issues in the biosimilar space.

Legal challenges, drug shortages, and regulatory issues create hurdles for biosimilars in the US market.

More biosimilar approvals may lead to lower costs.

Douglas Samojedny, RPh, director of Pharmacy Operations at Pharmacy Advantage, discusses how biosimilars could impact specialty pharmacy into the immediate future.

Mylan gains global licenses for its biosimilar to trastuzumab (Herceptin).

While biosimilars have the potential to slow the dramatic rise in the overall drug spend, many questions need to be answered.

GP2017 observed to reduce symptoms among patients with moderate-to-severe chronic plaque psoriasis.

Over the last few months, new developments have taken place within the biosimilar market including new drug approvals and guidance documents released by the FDA.

The interchangeability designation demonstrates that the efficacy and safety of a biosimilar is equal to the reference product.

Application pulled for biosimilar that treats neutropenia.

Increased use of biosimilars could create sustainable care for multiple chronic diseases.

Utilization of biosimilars has the potential to overhaul cancer treatment.

Humira is currently approved to treat rheumatoid arthritis, inflammatory bowel disease, and psoriasis.

Agency releases guidelines to determine the interchangeability of biosimilars with their reference products.

Guidance intends to help sponsors demonstrate Interchangeability with a reference product.

Requirements will vary based on the nature of the proposed interchangeable product, and may include an evaluation of data and information generated to support a demonstration of a biological product’s biosimilarity.

Biological products will be designated with 4-letter suffixes devoid of meaning.

FDA finalizes guidance for nonproprietary naming of biological products.

Top trends will include changing policies, pursuing value, and improving access to care.