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Jun 30, 2024

Equillium Q2 2024 Earnings Report

Equillium's financial performance for Q2 2024 was reported, featuring revenue growth and a strengthened cash position.

Key Takeaways

Equillium reported a net income of $0.5 million for the second quarter of 2024, a significant improvement compared to the net loss of $3.3 million in the same period of 2023. Revenue increased to $13.9 million, driven by itolizumab development funding and amortization of the upfront payment. The company's cash balance increased to $33.3 million.

Revenue for Q2 2024 was $13.9 million, up from $9.1 million in Q2 2023.

Net income for Q2 2024 was $0.5 million, compared to a net loss of $3.3 million in Q2 2023.

Cash, cash equivalents, and short-term investments totaled $33.3 million as of June 30, 2024.

Ono Pharmaceutical has an option to acquire Equillium’s rights to itolizumab, with a decision expected by the end of October 2024.

Total Revenue
$13.9M
Previous year: $9.12M
+51.8%
EPS
$0.01
Previous year: -$0.1
-110.0%
Gross Profit
$13.8M
Previous year: $9.09M
+52.0%
Cash and Equivalents
$33.3M
Previous year: $48.4M
-31.2%
Free Cash Flow
$668K
Total Assets
$42.9M
Previous year: $58.8M
-27.1%

Equillium

Equillium

Forward Guidance

Equillium anticipates several milestones, including Ono's option exercise decision, EQ101's transition to subcutaneous delivery and Phase 2 dose optimization study, and EQ302's Phase 1 study initiation.

Positive Outlook

  • Potential for Ono to exercise its option to acquire Equillium’s rights to itolizumab, resulting in a $35.0 million payment.
  • Advancement of EQ101 with transition to subcutaneous delivery and initiation of Phase 2 dose optimization study in alopecia areata.
  • Advancement of EQ302 with plans to initiate Phase 1 clinical development in the second half of next year.
  • Positive interim review of the Phase 3 EQUATOR study.
  • Positive topline data from Phase 2 study of EQ101 in subjects with alopecia areata.

Challenges Ahead

  • Uncertainty regarding Ono’s decision to exercise its option.
  • Potential delays in clinical trial timelines.
  • Risks associated with transitioning EQ101 to subcutaneous delivery.
  • Dependence on itolizumab development funding payments from Ono.
  • Potential for increased research and development expenses.