Halozyme Therapeutics, Inc., a biopharmaceutical company based in San Diego, has reported significant growth in financial and operational results for the first quarter ending March 31, 2024. The company has also provided updates on recent corporate activities and future projections.
In the first quarter of 2024, Halozyme achieved a revenue of $196 million, marking a 21% year-over-year increase primarily due to higher royalty and milestone revenues. Key financial results for the quarter include a net income of $77 million, an adjusted EBITDA of $116 million, GAAP diluted earnings per share (EPS) of $0.60, and non-GAAP diluted EPS of $0.79. Royalty revenue also increased by 21% to reach $121 million.
Operating expenses saw various changes: the cost of sales decreased to $28.3 million from $35.2 million in the previous year, primarily due to reduced bulk rHuPH20 sales. Research and development expenses increased slightly to $19.1 million, reflecting continued investment in
ENHANZE®, while selling, general, and administrative expenses decreased to $35.1 million due to lower marketing costs. The company reported an operating income of $95.5 million, significantly up from $53.8 million in the first quarter of 2023.
Halozyme's cash position also improved, with cash and marketable securities totaling $463.5 million on March 31, 2024, compared to $336 million at the end of 2023. This increase was mainly driven by cash flow from operations.
The company reiterated its financial guidance for the full year 2024, projecting total revenue between $915 million and $985 million, representing a growth of 10% to 19% from 2023. The expected adjusted EBITDA ranges from $535 million to $585 million, marking a year-over-year growth of 26% to 37%. Non-GAAP diluted EPS is projected to be between $3.55 and $3.90, reflecting a growth of 28% to 41%.
Significant corporate milestones were also highlighted, including the launch of a new $750 million share repurchase program. Several partner achievements were noted:
Bristol Myers Squibb's U.S. FDA acceptance of a Biologics License Application for a subcutaneous formulation of
Opdivo® (nivolumab) with ENHANZE®, and
Roche's receipt of a recommendation for the approval of
Ocrevus® (ocrelizumab) subcutaneous formulation for
multiple sclerosis by the European Medicines Agency, with a final decision anticipated in mid-2024.
Additionally, argenx initiated two registrational studies for
efgartigimod with ENHANZE® for
thyroid eye disease, and ViiV started a Phase 1 study for
VH4524184 with ENHANZE®.
Takeda also submitted a New Drug Application in Japan for
TAK-771, seeking approval for the treatment of
primary immunodeficiency.
Looking ahead, Halozyme remains optimistic about its growth trajectory. The company is focused on advancing its ENHANZE® drug delivery technology, which facilitates subcutaneous drug delivery, aiming to reduce treatment burdens for patients. Halozyme's technology is currently utilized in seven commercialized products across over 100 global markets, in partnership with leading pharmaceutical companies like Roche, Takeda,
Pfizer, and
Janssen. The company continues to invest in developing drug-device combination products to enhance patient convenience and adherence.
In conclusion, Halozyme Therapeutics has reported robust financial performance for the first quarter of 2024, driven by increased revenues and strategic partnerships. The company’s future outlook remains strong, backed by ongoing product developments and a solid financial position.
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