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Jun 30, 2024

Verrica Q2 2024 Earnings Report

Verrica reported second quarter 2024 financial results with YCANTH revenue of $4.9M and announced positive preliminary topline results of Phase 2 clinical study of VP-315.

Key Takeaways

Verrica Pharmaceuticals reported a net product revenue of $4.9 million in the second quarter of 2024, driven by YCANTH sales. The company is progressing with its clinical pipeline, including positive Phase 2 results for VP-315 and preparations for a Phase 3 trial for common warts. Net loss for the quarter was $17.2 million, or $0.37 per share.

Recognized net product revenue of $4.9 million in Q2 2024 from YCANTH.

Announced positive preliminary results from Phase 2 study of VP-315 for basal cell carcinoma.

Progressing towards global Phase 3 trial for YCANTH in common warts, expected to begin in 1H 2025.

Added Cencora, Inc. as a specialty distributor in Q2 2024 to grow YCANTH distribution.

Total Revenue
$5.18M
Previous year: $182K
+2744.5%
EPS
-$0.31
Previous year: -$0.21
+47.6%
Gross Profit
$4.64M
Previous year: $46K
+9976.1%
Cash and Equivalents
$31.9M
Previous year: $55.1M
-42.1%
Free Cash Flow
-$16.4M
Previous year: -$4.73M
+246.2%
Total Assets
$52M
Previous year: $62.2M
-16.4%

Verrica

Verrica

Forward Guidance

Verrica anticipates continued growth in YCANTH prescriptions throughout the latter half of 2024, driven by the receipt of a permanent J-Code, progress in removing unapproved cantharidin products from the market, growing insurance coverage, and expanded distribution capabilities.

Positive Outlook

  • Expect YCANTH prescription growth to continue quarter over quarter in the second half of 2024.
  • Permanent J-Code for YCANTH went into effect on April 1, streamlining product coverage and reimbursement.
  • Made progress in removing unapproved, compounded cantharidin distributed by Dormer Laboratories.
  • Growing insurance coverage for YCANTH.
  • Expansion of distribution capabilities.

Challenges Ahead

  • Uncertainties inherent in the drug development process and the regulatory approval process.
  • Reliance on third parties over which Verrica may not always have full control.
  • Risks and uncertainties described in Verrica's Annual Report on Form 10-K and Quarterly Report on Form 10-Q.
  • Potential for actual results to differ materially from forward-looking statements.
  • Verrica's ability to fund its operations into the first quarter of 2025.