Bringing Drug Costs Down in 2016 with Generics and Biosimilarsby Carissa - January 20th, 2016
Carissa Andrews is an passionate author and freelancer from Minnesotan with a focus in creative writing.
2016 is shaping up to be an interesting year for the pharmaceutical industry and for potential savings for consumers. Beyond the backlash, the US market has finally taken steps to approve a new type of medication that you may never have even heard of: Biosimilars.
What are Biosimilars?
In its basic form, a biosimilar drug is nothing more than a biologic drug; as opposed to a straight up small molecule (chemically synthesized) drug. The biosimilar drug is just like it sounds, intentionally created to be similar to its reference product. To understand how a biosimilar is different from a small molecule drug or even a standard generic drug, we need to understand the nature of biologic drugs themselves because that’s where the distinction lies. Biologic drugs are those whose active ingredients are made in a living system and are far more complex than small molecule drugs. This is because they’re generally derived from a living organism including humans, animals, microorganisms, yeast, or bacteria.
In order for a biosimilar to be approved, there’s still an extensive dance it must participate in with the FDA. While a typical drug has market exclusivity for five years, a biologic drug has twelve to recoup the costs involved with development and research. This goes to show just how much added efforts go into the complexity of a biologic medication. Not to get too complicated, but there are actually two types of biosimilar drugs:
1. Ones that are biosimilar, but have different indications than their reference product, and
2. Ones that are bioequivalent enough to be used interchangeably with their reference product. More on that in a minute.
Once patents and exclusivity runs out, and a biosimilar drug is ready to be considered, the FDA looks at the following definitions to determine whether or not to approve the drug.
FDA’s Definition of Biosimilarity:
• The biological product is highly similar to the reference product notwithstanding minor differences in clinically inactive components; and
• There are no clinically meaningful differences between the biological product and the reference product in terms of the safety, purity, and potency of the product.
• NOTE: A biosimilar will not always have the same indications for use as its reference biologic drug. It can also be granted indications different from those of the reference biologic product if a full clinical data is submitted for those indications.
FDA’s Definition of Interchangeability:
• The biological product is biosimilar to the reference product
• It can be expected to produce the same clinical result as the reference product in any given patient; and
• For a product to be administered more than once, the safety and reduced efficacy risks of alternating or switching are not greater than with use of the reference product without altering or switching.
• NOTE: The interchangeable product may be substituted for the reference product without the authorization of the health care prescriber. This is the main difference between biosimilar and interchangeable biosimilar in the United States.
March 6, 2015 brought about the era of biosimilar drugs to the United States when the first biosimilar drug was approved. Zarxio (filgrastim-sndz) by Sandoz is the only biosimilar FDA approved drug and based off of the reference product, Neupogen by Amgen. Though Zarxio shares 5 major indications with it’s reference, at this time it’s not considered to be interchangeable. So a prescription for the medication is still needed in order to use it.
How are Biosimilars Different from Generics?
Generics are small molecule drugs which are the pharmaceutical equivalence to their reference product and can be used interchangeably without a separate prescription.
Depending on what the biosimilar drug treats, it could be considered a biologic generic of sorts – but only if the indications are the same as its reference product and if the FDA approves the drug to be used interchangeably.
To be considered an interchangeable biosimilar is likely the goal for most companies producing biosimilars, but the FDA will likely require extensive clinical data to give such an approval. Once that threshold is met, the hope is to begin a healthy competition which will bring prices down on biologic drugs, just as generics have done for small molecule drugs.
In the meantime, a biosimilar could be used for the same indications, just as Zarxio is for a number of Neupogen’s indications, but it could either not be equivalent enough to be interchangeable or conceivably have better efficacy than their reference product – thus also denying its interchangeability.
Only time will tell just how much biosimilar drugs will end up affecting pricing down the road, but all indications are good that a more competitive market will produce a more competitive price structure, too. So while the politicians work their end to lower the costs of prescription drugs in the United States, generics and biosimilars may be another avenue toward cost savings for the average American. That’s something we can all get behind.
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