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Morning Briefing

Summaries of health policy coverage from major news organizations

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Monday, Jul 29 2019

Full Issue

Pfizer In Talks To Merge Its Off-Patent Drugs Business With Mylan To Create Generic Drug Giant

The deal, if completed, could be announced as early as Monday. The deal would bring together two businesses whose sales have slowed since former big sellers lost patent protection and began facing lower-priced competition. In other pharmaceutical news: black box warnings, antibiotics, and biotech's burning questions.

The New York Times: Pfizer Is Said To Plan A Deal For Its Off-Patent Drugs Unit

Pfizer is near a deal to combine its off-patent drugs division — which includes best-selling treatments like Viagra — with Mylan, the maker of the EpiPen emergency allergy treatment, to create a new giant in the business of drugs without patent protections, two people briefed on the matter said. A deal could be announced as soon as Monday, according to these people, who were not authorized to speak publicly about the confidential discussions. (de la Merced and Thomas, 7/28)

The Wall Street Journal: Pfizer Nears Deal To Combine Off-Patent Drug Business With Mylan

The deal, which hasn’t been completed, could be announced as early as Monday if an agreement is reached, the people said. The companies have discussed a stock deal in which Mylan shareholders would own a little more than 40% of the new entity and Pfizer shareholders the remainder, one of the people said. Pfizer would also receive about $12 billion in proceeds from a new sale of debt, this person said. Mylan’s market value currently stands at just under $10 billion. (Rockoff and Lombardo, 7/29)

Bloomberg: Pfizer And Mylan Are Near A Merger 

Michael Goettler, who runs Pfizer’s off-patent drug unit, would become chief executive of the combined company, and Mylan Chairman Robert Coury would be executive chairman, one of the people said. Current Mylan CEO Heather Bresch would depart. Mylan President Rajiv Malik, who faces civil suits accusing him of taking part in an alleged price-fixing scheme, would ultimately leave the combined company, one of the people said.(Annett and Griffin, 7/27)

Bloomberg: Pfizer’s Dealmaker CEO Sharpens Cancer Focus With Mylan Plan

Pharmaceutical behemoth Pfizer Inc. has transformed itself under new leadership through a series of spinouts and joint ventures, mitigating risk by placing some units at arm’s length while continuing to reap rewards from them. Chief Executive Officer Albert Bourla, 57, who took the helm in January after serving as the drugmaker’s operations chief, has rapidly transformed the company through a new deal-making strategy. His next major step may come as soon as Monday with a plan to combine Pfizer’s less-lucrative off-patent drug business with Mylan NV to form a generic-drug giant. (Griffin, 7/28)

The Wall Street Journal: FDA Requires Box Warnings For Pfizer Drug Xeljanz

The U.S. Food and Drug Administration is requiring that health warnings be added to Pfizer Inc. ’s drug Xeljanz, advising patients they could experience a higher risk of blood clots or death with a specific dose. The FDA’s warnings are specifically geared toward patients who take the 10-milligram dose of the medicine, known as tofacitinib, twice a day. The regulatory agency also said it is limiting the use of the treatment for ulcerative colitis so that patients can only take it if they have severe side effects from other medicines or aren’t treated effectively. (Prang, 7/26)

The Wall Street Journal: Antibiotics Companies Plot Course Past Market Obstacles

With investor interest in antibiotics dwindling, companies in the sector are crafting survival strategies that include seeking out alternative sources of funding and avoiding reliance on hospitals as customers. (Gormley, 7/26)

Stat: Answers To Some Of Biotech’s Burning Questions — And Issues To Watch

Last January, we compiled a list of “burning questions” for a group of the largest and most closely followed biotech companies. Answers to these questions — encompassing financial performance, clinical trial milestones, and regulatory approvals — can make or break a company’s performance during the year. August is almost here, so we figured it was a good opportunity to see how many of this year’s biotech burning questions have been answered, and what lies ahead. (Feuerstein and Garde, 7/29)

This is part of the Morning Briefing, a summary of health policy coverage from major news organizations. Sign up for an email subscription.
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