New clinical trial data demonstrates BD Libertas™ Wearable Injector as a drug delivery system

BD (Becton, Dickinson and Company), one of the leading global medical technology companies, has announced publication of the results from a 52-subject human clinical trial with the BD Libertas™ Wearable Injector. The subcutaneous drug delivery system, currently in final phases of development, is designed as ready-to-use to deliver drugs such as biologics with viscosities up to 50 cP in 2-5 mL and 5-10 mL configurations.

This research to evaluate the performance of the 5 mL BD Libertas™ device in human subjects, including tissue effects, skin reactivity and patient acceptance, confirms that the BD Libertas™ device delivered within an acceptable time period 5 mL of 8 cP injections to the abdomen and thigh regardless of subject age, gender, or BMI and with/without patient movement.

The application, use, and removal of the injector were found to be acceptable and 100% of subjects were likely to use the BD Libertas™ Wearable Injector if prescribed. No severe wheal, erythema, or bleeding was observed, and no unacceptable pain was noted at 24 hours post-injection.

The study represents the most recent in a series of over 50 BD-conducted pre-clinical and clinical studies intended to inform the design and measure the performance of the BD Libertas™ Wearable Injector, demonstrate feasibility of 2-10 mL biologic injections into subcutaneous tissue and characterize tissue response to large volume injections in human and animal subjects.

“These results show that BD Libertas™ Wearable Injector effectively delivers dose volumes up to 5 mL subcutaneously and may be leveraged by our pharmaceutical partners as a reliable platform for large volume delivery,” said Eric Borin, Worldwide President, BD Pharmaceutical Systems. “BD is committed to working with our customers and the broader pharmaceutical market to meet their needs by enabling an expanded drug delivery design space. We are excited to share these results further with our partners and the broader market, to help accelerate and de-risk combination product development.”

Biologics for subcutaneous delivery in larger dose volumes (>2mL) are now being developed by pharmaceutical companies to support life cycle management of therapies, including migration from intravenous to subcutaneous routes of administration. BD undertook this study, recognizing that limited clinical evidence exists in the public domain to support injection feasibility and tolerability with wearable injector solutions to deliver larger dose volumes (up to 5 mL).

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