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Halozyme Reports Second Quarter 2017 Results

-- Genentech's U.S. RITUXAN HYCELA™ Launch Underway; Lilly Doses First Patient in Clinical Study of New Investigational Therapy Combined with Halozyme ENHANZE® Technology --

-- Total Revenue of $33.8 million with Royalty Revenue Increase of 20 Percent from Prior-Year Period to $14.7 million --

SAN DIEGO, Aug. 8, 2017 /PRNewswire/ -- Halozyme Therapeutics, Inc. (HALO), a biotechnology company developing novel oncology and drug-delivery therapies, today reported financial results and recent highlights for the second quarter ended June 30.

"A clear highlight of the second quarter was approval of Genentech's RITUXAN HYCELATM in the U.S., and the resulting strong interest from new potential partners who seek to coformulate with our ENHANZE® technology," said Dr. Helen Torley, president and chief executive officer. "We have strong momentum in the ENHANZE® business with continued growth in royalties and a number of catalysts in the second half of 2017, including Lilly's recent start of their Phase 1 study, Janssen's upcoming start of their Phase 3 study of subcutaneous daratumumab and our expectation for a new collaboration agreement.

"At the same time, we are executing well in our HALO-301 study of PEGPH20 with screening and enrollment tracking to our expectations and investigator enthusiasm continuing to be strong. I also remain encouraged by recent progress screening and enrolling patients in the dose expansion portion of our Phase 1b study of PEGPH20 in combination with KEYTRUDA® and the recent initiation of Genentech's study of PEGPH20 with TECENTRIQ®.

"With strategic and operational progress across both pillars, we look forward to the potential for additional value inflecting events in the coming months."

Second Quarter 2017 and Recent Highlights include:

  • Approval of Genentech's RITUXAN HYCELA by the Food and Drug Administration (FDA). The combination of rituximab and Halozyme's hyaluronidase human ENHANZE® technology has been approved for patients with follicular lymphoma, diffuse large B-cell lymphoma and chronic lymphocytic leukemia and is now available to patients in more than 60 countries worldwide.
  • Eli Lilly initiating a Phase 1 study of an investigational new therapy in combination with Halozyme's ENHANZE® technology as part of the companies' 2015 Global Collaboration and Licensing agreement.
  • Johnson and Johnson highlighting progress with the subcutaneous formulation of DARZALEX® (daratumumab) during their 2017 Pharmaceutical Business Review. The formulation, which uses Halozyme's ENHANZE® technology to enable a 5-minute infusion, is currently being studied in a Phase 1b clinical trial and planned to begin a Phase 3 study later this year.
  • Progress in the HALO-301 study of PEGPH20 in combination with ABRAXANE® (nab-paclitaxel) and gemcitabine in first line metastatic pancreas cancer patients with high levels of tumor hyaluronan (HA-High). Screening and enrollment in the study continues to track in line...