Sep 30, 2022

Journey Medical Q3 2022 Earnings Report

Reported a decrease in revenue due to generic competition of Targadox, and are progressing with DFD-29 clinical trials.

Key Takeaways

Journey Medical reported a decrease in revenue for Q3 2022 compared to Q3 2021, primarily due to generic competition of Targadox. However, the company is progressing with its DFD-29 Phase 3 clinical program and anticipates top-line data in the first half of 2023.

Revenue for Q3 2022 was $16.1 million, compared to $19.6 million for Q3 2021.

The decline in revenue was primarily attributed to generic competition of Targadox and an increase in net revenue of Accutane.

75% enrollment achieved in DFD-29 Phase 3 clinical program for papulopustular rosacea.

Top-line data from the DFD-29 Phase 3 clinical program is anticipated in the first half of 2023.

Total Revenue
$16.1M
Previous year: $19.6M
-17.8%
EPS
-$0.23
Previous year: $0.32
-171.9%
Gross Profit
$8.9M
Previous year: $8.44M
+5.4%
Cash and Equivalents
$34.9M
Previous year: $21.7M
+60.9%
Total Assets
$108M
Previous year: $89.1M
+21.4%

Journey Medical

Journey Medical

Forward Guidance

Journey Medical expects to report record revenue for the full year 2022 and anticipates DFD-29 will achieve peak annual net sales exceeding $100 million after approval.

Positive Outlook

  • Expect to report record revenue for the full year 2022.
  • Anticipate announcing top-line data from the DFD-29 trials in the first half of 2023.
  • Expect to file a New Drug Application in the second half of 2023.
  • Anticipate that DFD-29 will achieve peak annual net sales exceeding $100 million.
  • Plan to launch another product in the upcoming months.

Challenges Ahead

  • Sales revenue for Q3 2022 continues to be negatively impacted primarily by the effect of Targadox generic competition versus Q3 2021.
  • Cybersecurity breach in September 2021 resulted in losses of $9.5 million.
  • The process to recover funds from the cybersecurity breach could take as long as 6 months or more to complete.
  • Uncertainties relating to preclinical and clinical testing.
  • Risks relating to the timing of starting and completing clinical trials, including disruptions that may result from hostilities in Europe.