Halozyme Therapeutics, Inc. develops and commercializes drug-delivery technologies for subcutaneous administration of biologics and other injectable therapies. News about HALO commonly covers ENHANZE licensing agreements, Hypercon and Surf Bio hyperconcentration collaborations, partner product regulatory approvals, royalty-based revenue updates, and financial guidance.
The company also reports developments tied to its proprietary products Hylenex and XYOSTED, drug-device combination products using auto-injector technologies, and collaborations with pharmaceutical and biotechnology companies in oncology, inflammatory disease and other therapeutic areas.
Halozyme Therapeutics, Inc. (NASDAQ: HALO) announced that Dr. Helen Torley, CEO, will participate in a fireside chat at the Piper Sandler 32nd Annual Virtual Healthcare Conference from December 1-3, 2020. The pre-recorded chat will be accessible on November 25 via the company’s investor relations website. Halozyme focuses on innovative biopharmaceutical solutions, primarily using its proprietary ENHANZE® technology, which enhances drug delivery and has positively impacted over 400,000 patients globally. The company partners with major pharmaceutical firms to develop new therapies, enhancing patient experiences and outcomes.
Summary not available.
Halozyme Therapeutics (NASDAQ: HALO) announced that Janssen Pharmaceutical submitted applications to both the FDA and EMA for the approval of DARZALEX FASPRO™ subcutaneous formulation. This treatment, aimed at relapsed or refractory multiple myeloma patients, allows administration in 3-5 minutes, vastly reducing the time from the traditional intravenous method. The application is backed by positive results from the Phase 3 APOLLO study suggesting longer progression-free survival compared to the standard treatment. The full study results will be presented at the ASH Annual Meeting on December 6, 2020.
Halozyme Therapeutics (NASDAQ: HALO) has announced that key studies sponsored by Janssen Research & Development will be presented at the American Society of Hematology (ASH) Annual Meeting from December 5-8, 2020. The Phase 3 APOLLO study will feature an oral presentation on December 6 at 3:00 p.m. ET, discussing subcutaneous daratumumab with pomalidomide and dexamethasone in multiple myeloma patients. The ANDROMEDA study results will be presented on December 7, also in an oral format, along with four additional poster presentations.
Halozyme Therapeutics, Inc. (NASDAQ: HALO) reported robust financial results for Q3 2020, achieving a revenue of $65.3 million, up from $46.2 million year-over-year. The growth was driven by $32.0 million in collaboration revenue and a 44% rise in royalties. The company's net income was $36.2 million, marking a significant turnaround from a net loss in the prior year. Halozyme also raised its full-year revenue guidance to $250 million-$260 million, reflecting a projected 28-33% growth. The company has repurchased $312.4 million in shares, reinforcing its commitment to capital return.
Halozyme Therapeutics, Inc. (NASDAQ: HALO) will host a webcast for its third-quarter 2020 financial results on November 2, 2020, at 4:30 p.m. ET. The call, led by CEO Dr. Helen Torley, follows the release of the financial results for the quarter ending September 30, 2020.
Investors can register through a provided link, with a replay available for two weeks post-call. Halozyme utilizes its ENHANZE® technology, enhancing drug delivery, to partner with major pharmaceutical firms and positively impact patient outcomes globally.
Halozyme Therapeutics (NASDAQ: HALO) has expanded its collaboration with argenx, adding exclusive access to its ENHANZE® drug delivery technology for three new targets. This brings the total to six targets under the agreement initiated in February 2019. argenx is advancing the development of its FcRn antagonist efgartigimod and has also nominated a complement inhibitor targeting C2. The collaboration aims to improve patient experiences by enabling subcutaneous delivery options for various therapies. Halozyme derives revenues through milestones and royalties from these partnerships.
Halozyme Therapeutics (NASDAQ: HALO) announced that Roche presented data from the Phase 1b study evaluating atezolizumab (Tecentriq) for subcutaneous use through Halozyme's ENHANZE technology at the ESMO Virtual Congress 2020. The study, involving 67 patients with advanced non-small cell lung cancer, showed that the subcutaneous formulation was well-tolerated and had similar exposure to the intravenous version. This supports further development in the Phase 3 study, potentially improving treatment efficiency by reducing administration time.
Halozyme Therapeutics announced that Janssen Biotech submitted a supplemental Biologics License Application (sBLA) to the FDA for DARZALEX FASPRO (daratumumab and hyaluronidase-fihj) to treat light chain (AL) amyloidosis, a serious disease with no approved therapies. The application is backed by positive results from the Phase 3 ANDROMEDA study, which achieved its primary endpoint. This sBLA is evaluated under the FDA's Real-Time Oncology Review program, aiming for expedited patient access to treatments. The approval process does not guarantee success.
Halozyme Therapeutics (NASDAQ: HALO) announced that Dr. Helen Torley, President and CEO, will participate in two upcoming investor conferences. The first is the Cantor Virtual Global Healthcare Conference scheduled for September 15, 2020, at 10:40 a.m. ET, and the second is the Morgan Stanley Virtual Global Healthcare Conference on September 17, 2020, at 2:00 p.m. ET. Live webcasts of both events will be available on Halozyme's website, along with an archive for 90 days post-event. Halozyme specializes in biopharmaceutical solutions, notably through its ENHANZE® technology.