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Dec 31, 2021

Cytokinetics Q4 2021 Earnings Report

Cytokinetics reported a net loss and increased revenue due to license revenue from Ji Xing.

Key Takeaways

Cytokinetics reported a net loss of $30.6 million for Q4 2021, with revenues increasing to $55.6 million compared to $6.7 million in the same period of 2020, primarily driven by license revenue from Ji Xing. The company's cash balance reached $623.7 million at the end of the year, and they anticipate revenue between $20 to $25 million for 2022.

Net loss for Q4 2021 was $30.6 million, or $0.36 per share.

Revenues for Q4 2021 increased to $55.6 million, up from $6.7 million in Q4 2020.

Cash, cash equivalents, and investments totaled $623.7 million as of December 31, 2021.

The company anticipates revenue between $20 to $25 million for 2022.

Total Revenue
$55.6M
Previous year: $6.72M
+727.1%
EPS
-$0.36
Previous year: -$0.62
-41.9%
Gross Profit
$12.1M
Previous year: -$22.5M
-153.8%
Cash and Equivalents
$624M
Previous year: $501M
+24.5%
Free Cash Flow
-$62.5M
Previous year: $45.6M
-237.1%
Total Assets
$841M
Previous year: $534M
+57.6%

Cytokinetics

Cytokinetics

Forward Guidance

Cytokinetics provided financial guidance for 2022, anticipating revenue between $20 to $25 million, operating expenses in the range of $380 to $400 million, and net cash utilization of approximately $365 to $385 million.

Positive Outlook

  • Revenue expected to be between $20 to $25 million.
  • Cash balance of $724 million, providing more than two years of runway.
  • Committed capital expected upon dosing of the first patient in SEQUOIA-HCM.
  • Focus on expanding the development program for aficamten.
  • Advancing the pipeline of early drug candidates.

Challenges Ahead

  • Operating expenses expected to be in the range of $380 to $400 million.
  • Net cash utilization expected to be approximately $365 to $385 million.
  • Potential difficulties or delays in development and regulatory approvals.
  • Patient enrollment for clinical trials may be difficult or delayed.
  • The FDA or foreign regulatory agencies may delay or limit clinical trials.