β€’
Mar 31, 2024

Inozyme Q1 2024 Earnings Report

Inozyme reported financial results for the first quarter ended March 31, 2024 and provided business highlights.

Key Takeaways

Inozyme Pharma reported a net loss of $23.3 million, or $0.38 loss per share, for the quarter ended March 31, 2024. The company's cash, cash equivalents, and short-term investments were $166.2 million as of March 31, 2024, which are expected to fund operations into the fourth quarter of 2025.

Positive topline data from Phase 1/2 clinical trial of INZ-701 in adults with ABCC6 Deficiency, showing improvements in vascular pathology, visual function, and patient reported outcomes.

Initial findings from natural history studies indicate a substantial disease burden among pediatric patients with ABCC6 Deficiency, with a high incidence of major clinical events.

Positive topline data from Phase 1/2 clinical trial of INZ-701 in adults with ENPP1 Deficiency, showing maintained favorable safety, immunogenicity, and clinical outcome data through 48 weeks.

Cash, cash equivalents, and short-term investments were $166.2 million as of March 31, 2024, expected to fund operations into the fourth quarter of 2025.

Total Revenue
$0
EPS
-$0.38
Previous year: -$0.4
-5.0%
Gross Profit
-$182K
Cash and Equivalents
$166M
Previous year: $131M
+26.9%
Free Cash Flow
-$24.6M
Previous year: -$17.9M
+36.9%
Total Assets
$177M
Previous year: $142M
+24.8%

Inozyme

Inozyme

Forward Guidance

Inozyme anticipates several milestones including interim data from SEAPORT-1, interim data from ENERGY-1, and initiation of the ENERGY-2 pivotal trial in infants.

Positive Outlook

  • Interim data from SEAPORT-1, a Phase 1 trial of INZ-701 in patients with end-stage kidney disease receiving hemodialysis, on track for fourth quarter of 2024.
  • Interim data from ENERGY-1, a Phase 1b trial of INZ-701 in infants with ENPP1 Deficiency, on track for second half of 2024.
  • Initiation of the ENERGY-2 pivotal trial in infants, Ex-U.S. – 2H 2024
  • Topline data from the ENERGY-3 pivotal trial in pediatric patients – Mid-2025
  • Initiation of pivotal clinical trial in pediatric patients with ABCC6 Deficiency, subject to regulatory review and sufficient funding – Q1 2025