FTC’s Take On Two Pharma Mergers Shows Deals Can Clear Higher Hurdle

Pfizer’s acquisition of Arena without FTC intervention and Hikma’s acquisition of Custopharm with one product divestiture shows the commission is bound by anticompetitive facts of a deal. A more controversial merger may not get through, former FTC attorney says.

Hurdle
Pharma mergers are clearing higher FTC hurdles • Source: Alamy

The US Federal Trade Commission has indicated that biopharma mergers would have a tougher time clearing the agency. But it’s decision not to intervene in Pfizer Inc.’s $6.7bn acquisition of Arena Pharmaceuticals, Inc. and its requirement for a single pipeline product divestiture as a condition of Hikma Pharmaceuticals plc’s acquisition of Custopharm, Inc. show that such deals can go through despite the agency’s closer scrutiny and consideration of broader anticompetitive factors.

Some analysts had questioned if Pfizer’s deal with Arena would be accepted by the FTC given Pfizer’s substantial presence in immunology and inflammation. Arena’s etrasimod, in development across a range of immuno-inflammatory conditions, was at the heart of the deal. Pfizer argued that the drug is complementary to its current portfolio and not overlapping, and that the deal would bring a differentiated mechanism of action to market

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Generics

More from Biosimilars & Generics

US FDA Shows Support For Generic Drug User Fee Goals Amid Cutbacks

 

The FDA struck an upbeat tone during its annual Generic Drugs Forum despite an unprecedented period of cutbacks and disruptions and reiterated a desire to continue meeting user fee goals.

EU Biosimilar Filings, Opinions And Approvals

 

A list of EU biosimilar filings, CHMP opinions and EU marketing authorizations, including details of the biosimilar company, the brand name/INN, indication(s), the reference product/company, and the date and type of event.

Pulling Together: Global Regulators Discuss Convergence On Biosimilars

 
• By 

While the biosimilars industry has welcomed individual pockets of progress around regulatory streamlining, it is essential that approaches from global authorities move forward together if they are to have a meaningful impact on biosimilar development. At Medicines for Europe’s annual biosimilars conference, regulators from around the world talked about how their thinking is converging.