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Johnson & Johnson says FTC probing antitrust efforts around arthritis drug Remicade

Johnson & Johnson consequences on a shelf in a store in New York.

Lucas Jackson | Reuters

The Federal Trade Commission issued civil subpoenas to Johnson and Johnson in June as separate of an investigation into whether contracting practices for its blockbuster rheumatoid arthritis drug, Remicade, violated antitrust laws, the players said in a regulatory filing on Monday.

Shares of the company traded marginally down at $132.47, after having minuscule up 1.7% on Monday.

J&J said that the FTC had issued a “civil investigative demand,” or CID, the equivalent of a subpoena to determine if the contracting applications were legal.

Pfizer filed a lawsuit against J&J in 2017, saying its rivals contracts with health insurers for blockbuster rheumatoid arthritis deaden, Remicade, were anticompetitive and aimed at blocking sales of Pfizers biosimilar called Inflectra.

Pfizer said in the lawsuit that J&J had compact with many insurers to give discounts in exchange for giving preference to Remicade, and to only pay for Inflectra in cases where Remicade tried to be ineffective. Inflectra was approved in 2016 while Remicade went on the market in 1998.

Remicade is an infused treatment for chronic autoimmune shake ups and costs about $4,000 per dose, or $26,000 a year, Pfizer said in the lawsuit.

J&J has denied any wrongdoing and is fighting the Pfizer lawsuit.

Pfizer mentioned in a statement that it had received a CID in June.

“As Pfizers complaint alleges, J&Js unlawful conduct is designed to prevent Inflectra from being capable to compete on its primary point of differentiation price. Today, Inflectra has an average selling price (ASP) that is more than 22% lower than Remicade,” the entourage said in a statement. “Despite these facts, J&J has not lost substantial volume or share of sales counter to what should come to pass in a competitive market.”

Biosimilars are intended to be lower-cost alternatives to expensive biotech medicines. But since they are made from animate cells and it is not possible to make an exact copy of the branded medicine, they are not automatically substituted for the existing branded dope the way a generic drug would be.

The drugs treat ailments like rheumatoid arthritis, Crohn’s disease and ulcerative colitis.

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