Dec 31, 2020

Revance Q4 2020 Earnings Report

Reported financial results for the fourth quarter and full year ended December 31, 2020, and provided a corporate update.

Key Takeaways

Revance Therapeutics, Inc. reported strong fourth-quarter results, driven by the commercial launch of the RHA® Collection of dermal fillers and the HintMD fintech platform. The company's revenue increased significantly compared to the same period in 2019, and they exited 2020 with a substantial cash balance, positioning them for continued growth and pipeline advancement.

Total revenue for the fourth quarter reached $11.1 million, a significant increase from $0.1 million in the same period of 2019.

RHA® Collection of dermal fillers contributed $10.0 million in product revenue during the quarter.

Selling, general, and administrative expenses increased to $55.8 million due to commercial launch activities and the HintMD acquisition.

Cash, cash equivalents, and short-term investments totaled $436.5 million at year-end, providing funding into 2024.

Total Revenue
$11.1M
Previous year: $89K
+12409.0%
EPS
-$1.24
Previous year: -$0.99
+25.3%
Gross Profit
$7.47M
Previous year: -$20.6M
-136.3%
Cash and Equivalents
$334M
Previous year: $171M
+94.9%
Free Cash Flow
-$320M
Previous year: -$33.8M
+846.1%
Total Assets
$720M
Previous year: $340M
+111.7%

Revance

Revance

Forward Guidance

Revance anticipates several key milestones in 2021, including potential BLA approval for DaxibotulinumtoxinA for Injection, a new product extension for the RHA® Collection, the integration of PayFac into HintMD, and the completion of a Phase 3 study for cervical dystonia. The company projects GAAP operating expenses of $375 million to $390 million and non-GAAP operating expenses of $270 million to $285 million for 2021.

Positive Outlook

  • BLA approval for DaxibotulinumtoxinA for Injection in glabellar lines anticipated in 2021.
  • Release of the next-generation HintMD fintech platform, including PayFac integration, planned for mid-2021.
  • Teoxane SA submitted the pre-market approval application for RHA® 1 for perioral (lip) lines, with FDA approval expected in the second half of 2021.
  • Topline results from the ASPEN-OLS Phase 3 open-label safety study for cervical dystonia expected in the second half of 2021.
  • End-of-Phase 2 meeting with the FDA planned as the next step for upper limb spasticity.