Severe Hypertriglyceridemia (SHTG)
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Enrollment continues to progress well in ENTRUST, the Phase 3 trial evaluating the efficacy, safety and
tolerability of pegozafermin in patients with SHTG. Topline results from this trial are expected in 2025. |
Corporate Updates
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Completed follow-on offering in the fourth quarter of 2023 for
$172.5 million in gross proceeds. |
Fourth Quarter 2023 Financial Results
Cash Position. As of December 31, 2023, 89bio had cash, cash equivalents and marketable securities totaling $578.9 million, as compared to
$188.2 million as of December 31, 2022.
Research and Development (R&D) Expenses. R&D expenses were $33.6 million and
$122.2 million for the three months and year ended December 31, 2023, respectively, compared to $19.1 million and $80.8 million for the three months and year ended December 31, 2022, respectively. The increase in R&D
expenses for the year was primarily driven by increases in contract manufacturing costs and personnel-related expenses.
General and Administrative
(G&A) Expenses. G&A expenses were $7.6 million and $29.0 million for the three months and year ended December 31, 2023, respectively, compared to $6.3 million and $21.5 million for the three months and year ended
December 31, 2022, respectively. The increase in G&A expenses for the year ended December 31, 2023, was primarily due to an increase in personnel-related expenses, employee headcount, including stock-based compensation expense, and
increased consultant and professional service fees, partially offset by a decrease in insurance-related costs.
Net Loss. 89bio reported a net loss
of $40.2 million and $142.2 million for the three months and year ended December 31, 2023, respectively, compared to a net loss of $24.6 million and $102.0 million for the three months and year ended December 31, 2022,
respectively. The increase in net loss is primarily attributable to increased R&D expenses to advance the companys programs, increased G&A expenses associated with additions in headcount, and expenses in support of the companys
expanded operations, offset by an increase in interest income.
The foregoing financial information is unaudited and subject to change, and actual results
may vary from the foregoing.
About 89bio
89bio is a
clinical-stage biopharmaceutical company dedicated to the development of best-in-class therapies for patients with liver and cardiometabolic diseases who lack optimal
treatment options. The company is focused on rapidly advancing its lead candidate, pegozafermin, through clinical development for the treatment of nonalcoholic steatohepatitis (NASH) and severe hypertriglyceridemia (SHTG). Pegozafermin is a
specifically engineered, potentially best-in-class fibroblast growth factor 21 (FGF21) analog with unique glycoPEGylated technology that optimizes biological activity
through an extended half-life. Pegozafermin has been granted Breakthrough Therapy Designation for the treatment of NASH with fibrosis from U.S. Food and Drug Administration (FDA). The company is headquartered in San Francisco. For more information,
visit www.89bio.com or follow the company on LinkedIn.