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Halozyme Therapeutics — Jan 8, 2025 release

Fiscal 2024 fourth-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001159036-25-000003
Open on SEC.gov ↗
Showing in the filing
New Accelerated Share Repurchase (ASR) program
“$250 million”
Period
No period stated
Measure
Declared action
Source
Prose
All guidance in this release · 7
New Accelerated Share Repurchase (ASR) program
“$250 million”
Total revenue for FY2025
“$1,150 million to $1,225 million”
Revenue from royalties for FY2025
“$725 million to $750 million”
Adjusted EBITDA for FY2025
“$755 million to $805 million”
Non-GAAP diluted earnings per share for FY2025
“$4.95 to $5.35”
Royalty Revenue for FY2025
“$725 to $750 million”
Non-GAAP Diluted EPS for FY2025
“$4.95 to $5.35”
Exhibit 99.1 · the passage around this item
… earlier in the release
lion, Representing YoY Growth of 16% - 23%, Adjusted EBITDA of $755 - $805 million, Representing YoY Growth of 24% - 32%, and non-GAAP Diluted EPS of $4.95 - $5.35, Representing YoY Growth of 21% - 30% 1,2 Announces New $250 million Accelerated Share Repurchase Conference Call Scheduled Today at 5:30am PT/8:30am ET SAN DIEGO, January 8, 2025 -- Halozyme Therapeutics, Inc. (NASDAQ: HALO) (“Halozyme” or the “Company”) today provided a financial update, reiterating full year 2024 financial guidance and raising full year 2025 and multi-year financial guidance. The Company also announced it has recently entered into a new $250 million accelerated share repurchase (ASR) program under its previously announced $750 million share repurchase program. “Halozyme is at the forefront of drug delivery innovation, fostering a high-growth and durable business underpinned by our proprietary ENHANZE drug delivery technology. This leadership position is reflected in the global launch of nine ENHANZE co-formulated products, a robust pipeline and continuing interest from potential new partners,” said Dr. Helen Torley, president and chief executive officer. “Our 2025 guidance, with projected revenue growth of 16% to 23% and adjusted EBITDA growth of 24% to 32%, is largely driven by VYVGART Hytrulo, which has received strong early acceptance in generalized myasthenia gravis, and is now seeing growing adoption in CIDP following the J
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.