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Halozyme initiates morphine study with Hylenex

Biopharmaceutical company Halozyme Therapeutics has dosed its first patient in a clinical trial evaluating subcutaneous administration of morphine with its spreading agent Hylenex.

Hylenex is a liquid injectable formulation that includes the active pharmaceutical ingredient, recombinant human hyaluronidase (rHuPH20). Morphine is a widely used drug for pain management and is currently approved for both intravenous and subcutaneous administration.

More rapid absorption facilitated by Hylenex via the subcutaneous (SC) route of administration could shorten the time of onset for achieving effective pain relief for patients, without the burden of intravenous (IV) administration.

Halozyme’s product is approved for use as a spreading agent to accelerate the delivery of fluids and drugs, such as local anesthesics, contrast agents, and for subcutaneous fluid replacement.

The morphine study is designed to determine the time to maximal blood levels of morphine after subcutaneous administration with and without Hylenex, and to assess safety and tolerability. The placebo-controlled crossover study will enroll up to 18 subjects.