Vials vs. Dual-Chamber Systems

For freeze-dried drugs, packaging makes the difference

By Thomas Otto, Managing Director, Vetter

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Freeze-dried products are currently omnipresent and gaining more and more ground in the pharmaceutical market. If international pharmaceutical and biotech industries want to keep up, they are compelled to reconsider their strategies. In the past few years, no fewer than 30% of all FDA approvals for parenteral drugs were given for lyophilized products. Market research is even predicting that 50% of all parenteral drugs will be lyophilized in the future. For the manufacturers involved, the major change lies in the challenges affecting the choice of packaging.

Lyophilization is particularly advantageous for complex and highly sensitive substances. For instance, freeze-drying increases a drug’s resistance to heat, light, and other external influences. Development, manufacturing and delivery of such substances, however, demands different requirements than with liquid formulations. Galenic formulation for example, requires other excipients, while manufacturing demands efficient freeze-drying cycles. Also, the drug has to be reconstituted completely and safely immediately prior to administration.

Lyophilized drugs require manufacturers to think carefully about what kind of packaging their product will need; usually vials or dual-chamber systems, with the latter being either syringes or cartridges. These two systems involve different manufacturing processes and, later delivery steps. Each offers specific opportunities that depend on the competitive situation. When determining the most adapted packaging for the chosen system, companies should take into consideration three critical factors:

• The market – What other drugs are available, and in what drug delivery system?
• The user – Who will be performing the injection, and will the user group be expanded to the homecare segment at a later date?
• Packaging know-how – Does the company itself or a contract development and manufacturing organization (CDMO) dispose of efficient production technologies and innovative injection systems?

Vials are a good option if the product is a genuine innovation with no visible competition in the medium-term. They are less complex than other options, and the manufacturing processes are fairly standard. Choosing vials reduces time-to-market which, in turn, optimizes the duration of patent protection.

At the same time, vials require experience for the reconstitution of the drug and for producing an accurate dosage. If the user group includes not only doctors and nursing staff, but also patients and/or their relatives, then companies have the option of using auxiliary devices. For example, vials can be equipped with adapters that make reconstitution far easier to manage. Some CDMOs also have prefilled syringes with sterile water for injections (sWFI) in their portfolio.

For users with little practice, these combinations provide an adequate and reliable solution. The systems are built to produce the precise dose of reconstituted substances, therefore, adapters and sWFI syringes are an option to support all user groups. When competitors appear on the market at a later stage, a company’s product can then be differentiated by greater user-friendliness. Of course, this only applies if the competitor’s drug has also been lyophilized and packaged in a vial.

The previously mentioned scenario applies solely to genuine innovations. These innovations are becoming rarer as the industry moves away from the remunerative blockbuster model. That is why companies must carefully scrutinize the competitive landscape that will be using their drug. IMS Health, a market research institute recently published a forecast report entitled: “The Global Use of Medicines: Outlook Through 2016.” The report states that in the next three years about one-third of all new molecular entities will be in the follower therapies category. The IMS report also predicts an increase in the share of generics to 35 percent of the entire market. Thus, it is critical that manufacturers use every possible opportunity to differentiate themselves from the competition.
The choice of packaging is one such opportunity. Defining a proper packaging strategy early in the process is one way to stave off competition both in the present and the future. If lyophilized drugs are also available in similar delivery systems, using a dual-chamber system like those offered by some CDMOs could be a recipe for success. They allow reconstitution directly inside the system be it a syringe or a cartridge. The lyophilized substance is located in one chamber and the diluent in the other. The drug is reconstituted just before administration. It is a simple and controllable process completed in a few easy steps. And it eliminates the more complex vial solution which requires a needle and enough experience to draw up the exact amount required.

Innovative syringes and cartridges also represent product differentiation vis-à-vis vials. For the professionals, they simplify the process and save time. Regarding the number of applications, doctors and caregivers save valuable time in the treatment and care of patients. In addition, the all-in-one-system reduces the risk of needle stick injuries which can represent a problem with vials.

The dual-chamber systems also open the way to entirely new segments such as the homecare market. Thanks to the injection systems, patients and their relatives can perform the injections themselves if need be, without fear of erroneous dosage. This is a genuine relief, particularly for patients who have to take medication themselves over longer periods. Of course, this particular segment includes unpracticed users with chronic illnesses. Such users often have the necessary experience, but their illness means they are less able to inject themselves due to declining muscular skills. All-in-one systems will then mean safer self-medication.

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