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Dec 31, 2023

scPharmaceuticals Q4 2023 Earnings Report

scPharmaceuticals reported Q4 2023 financial results and provided a business update.

Key Takeaways

scPharmaceuticals reported Q4 2023 net FUROSCIX® revenue of $6.1 million, representing a 61% sequential growth from Q3 2023. The company ended the year with $76 million in cash, cash equivalents, and short-term investments.

Net FUROSCIX revenue was $6.1 million, up 61% sequentially compared to Q3 2023.

Total FUROSCIX doses written reached 13,542, a 56% sequential increase.

FUROSCIX doses filled totaled 7,016, up 44% sequentially.

The company ended Q4 with cash, cash equivalents, and short-term investments of $76.0 million.

Total Revenue
$6.1M
EPS
-$0.35
Previous year: -$0.27
+29.6%
Gross Profit
$4.32M
Cash and Equivalents
$76M
Previous year: $118M
-35.8%
Free Cash Flow
-$15.2M
Previous year: -$11.8M
+28.4%
Total Assets
$94.5M
Previous year: $124M
-23.9%

scPharmaceuticals

scPharmaceuticals

scPharmaceuticals Revenue by Segment

Forward Guidance

scPharmaceuticals is on track to initiate a pivotal pharmacokinetic (PK) study in Q2 to support development of an 80mg/1mL auto-injector and plans to submit an sNDA to the FDA next month seeking expansion of the FUROSCIX indication to include patients suffering from chronic kidney disease (CKD).

Positive Outlook

  • Initiate a pivotal pharmacokinetic (PK) study in Q2 to support development of an 80mg/1mL auto-injector.
  • If successful, submit a New Drug Application (NDA) to the FDA by the end of 2024.
  • Submit an sNDA to the FDA next month seeking expansion of the FUROSCIX indication to include patients suffering from chronic kidney disease (CKD).
  • Continue to see sales of FUROSCIX to integrated delivery networks (IDNs).
  • FUROSCIX acceptance and utilization among heart failure specialists is accelerating.

Challenges Ahead

  • Anticipate that the GTN discount will increase over time as contracting efforts continue to evolve and mature.
  • Dependence on the commercial success of FUROSCIX.
  • Risks related to the receipt of regulatory approval for product candidates.
  • Risks related to the ability to manufacture sufficient product for commercialization.
  • Risk that global economic factors and uncertainties will impact the Company’s operations.