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used with a wide variety of drugs, making it easier for drugs that usually must be infused intravenously to instead be injected just beneath the skin, which makes it possible for patients to more conveniently inject themselves at home. In effect, the enzyme is intended to accelerate the distribution and cellular absorption of immunoglobulin and other large-molecule, biologic drugs.
The San Diego company also has been working with Roche to develop injectable versions of the cancer drugs trastuzumab (Herceptin) and rituximab (Rituxan). In a statement emailed to Reuters, Halozyme said Roche officials do not believe the FDA query will impact its program at this time. But Roche has been developing combined versions of the two cancer drugs for use in Europe.
“Halozyme made it sound like the request for additional data was not a big deal, and they made it sound like the issue the FDA was having was specific to the Baxter product,” Brad Loncar, a Halozyme shareholder, told me this afternoon. “With today’s news, the truth has come out. It’s clear that it’s a much bigger problem than they had previously indicated. They are testing this enzyme with multiple drugs and multiple partners.’
“The uncertainty level on a scale of one to 10 right now is like a 10,” Loncar said.
ViroPharma said it plans to proceed with studies of its C1 esterase inhibitor (Cinryze) as a stand-alone therapy. In a separate statement, ViroPharma says, “FDA stated that the issues are not specific to Cinryze and that ViroPharma could continue to evaluate subcutaneous administration of Cinryze without rHuPH20 [the Halozyme enzyme].