
Patent Cliff
A patent cliff is a colloquialism to denote the potential sharp decline in revenues upon patent expiry of one or more leading products of a firm. Additionally, for every drug that makes it to the market, a number of drugs never make it out of the lab or end up not being approved by the Food and Drug Administration (FDA). The exclusivity of the drug allows pharmaceutical companies to recoup losses from failed drugs. The world's biggest pharmaceutical firms, such as Pfizer (PFE) and GlaxoSmithKline (GSK), thus stand to lose billions of dollars in revenues and profits from the patent expiration on such blockbuster drugs as cholesterol drug Lipitor and asthma medication Advair respectively. Numerous firms have established profitable businesses by manufacturing generic alternatives to off-patent drugs, which can be sold at a fraction of the price of branded drugs. A patent cliff is a colloquialism to denote the potential sharp decline in revenues upon patent expiry of one or more leading products of a firm.

What Is a Patent Cliff?
A patent cliff is a colloquialism to denote the potential sharp decline in revenues upon patent expiry of one or more leading products of a firm. A patent cliff is when a firm's revenues could "fall off a cliff" when one or more established products go off-patent, since these products can be replicated and sold at much cheaper prices by competitors.
While it is applicable to any industry, in recent years the term "patent cliff" has come to be associated almost exclusively with the pharmaceutical industry.



Understanding Patent Cliffs
Currently, the term of a new patent in the U.S. is 20 years from the date on which the application for the patent was filed in the United States. Many other factors, however, can affect the actual duration of a patent.
Patent cliffs are the associated drops in revenue that can come when a firm sees a key product's patent expire. When this happens, a competing firm can bring substitutes for the product to the market more cheaply and easily, which takes market share from the original product. Developing a drug is a costly and time-consuming process, with sizeable research and development (R&D) expense.
Getting a drug approved is also an expensive and lengthy process with various clinical trials required to prove that the drug is safe. In recent years, costs have decreased due to advances in biotechnology and genomics. Additionally, for every drug that makes it to the market, a number of drugs never make it out of the lab or end up not being approved by the Food and Drug Administration (FDA).
The exclusivity of the drug allows pharmaceutical companies to recoup losses from failed drugs. Profit margins may seem impressive for a single brand-name drug, but it is much less impressive given that it subsidizes the cost of research and failed drugs. Once exclusivity ends, generic drug companies are allowed to produce the same drug, sold under a different brand name. The cost of a generic drug is significantly less for the consumer and the pharmacy. For both parties, generic drugs costs can be as much as 80% to 85% less than the name brand.
The world's biggest pharmaceutical firms, such as Pfizer (PFE) and GlaxoSmithKline (GSK), thus stand to lose billions of dollars in revenues and profits from the patent expiration on such blockbuster drugs as cholesterol drug Lipitor and asthma medication Advair respectively.
Patent Cliffs and Competition from Generics
Numerous firms have established profitable businesses by manufacturing generic alternatives to off-patent drugs, which can be sold at a fraction of the price of branded drugs. The "patent cliff" threat has spurred increasing consolidation in the pharmaceutical industry, as companies strive to replace blockbuster drugs whose patents are expiring with other drugs that have the potential to become big sellers.
Generic drug manufacturers have no significant research departments to subsidize. Instead, they simply have to copy the compounds used to manufacture the drug. The compounds are made public due to FDA regulations. Due to far lower research and development expenses, as well as a significantly lower burden for approval, the profit margins for generic drugs are higher despite significantly lower prices.
Related terms:
Bioequivalence
Bioequivalence represents the similarity between two drugs that have the same effect on a patient. read more
Biotechnology Industry ETF
A biotechnology industry exchange-traded fund (ETF) invests in companies that combine biology and technology to develop innovative products and services. read more
Biotechnology
Biotechnology is the scientific study using living organisms to develop healthcare products and processes. Learn how to invest in biotech companies. read more
Blockbuster Drug
A blockbuster drug is an extremely popular drug that generates annual sales of at least $1 billion for the company that sells it. read more
Food and Drug Administration (FDA)
The Food and Drug Administration is a government agency that regulates certain food, drugs, cosmetics, and medical products. read more
Generic Brand
A generic brand is a type of consumer product that lacks a widely recognized name or logo because it typically isn't advertised. read more
Orange Book
The Orange Book is a list of drugs that the U.S. Food and Drug Administration (FDA) has approved as both safe and effective. read more
Patent
A patent grants property rights to an inventor of a process, design, or invention for a set time in exchange for a comprehensive disclosure of the invention. read more
Research and Development (R&D)
Research and development (R&D) is a term to describe the effort a company devotes to the innovation, and improvement of its products and processes. read more