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Verrica Pharmaceuticals to Provide a Corporate Update and Report First Quarter 2024 Financial Results on May 13, 2024

Key Takeaway: Verrica Pharmaceuticals Inc. has announced a conference call and live webcast on May 13, 2024, to provide a corporate update and discuss its financial results for the first quarter of 2024. The company recently received FDA approval for its lead product, YCANTH™, to treat molluscum contagiosum, a contagious skin infection. Verrica continues to develop additional products for various dermatological conditions, showcasing its focus on medical interventions in dermatology.

Market Sentiment Analysis

POSITIVE FACTORS

  • Verrica Pharmaceuticals scheduled a corporate update and financial results meeting.
  • Company shows commitment to transparency with a scheduled call.
  • Verrica's lead product YCANTH™ has been FDA approved for treating molluscum contagiosum.

Full Press Release Details

WEST CHESTER, Pa., May 08, 2024 (GLOBE NEWSWIRE) -- Verrica Pharmaceuticals Inc. (“Verrica” or “the Company”) (Nasdaq: VRCA), a dermatology therapeutics company developing medications for skin diseases requiring medical interventions, today announced that it will host a conference call and live webcast at 8:30 a.m. ET on Monday, May 13, 2024 to provide a corporate update and discuss the Company's financial results for the first quarter ended March 31, 2024.
Individuals may participate in the live call via telephone by dialing 1-877-407-4018 (domestic) or 1-201-689-8471 (international) and using the conference ID: 13746100. Participants are asked to dial in 10 minutes before the start of the call to register.
A live audio webcast of the call be accessed by visiting the investor relations section of the Company’s website, www.verrica.com, or by clicking here. A replay of the webcast will be archived on Verrica’s website for 90 days following the event.
About Verrica Pharmaceuticals Inc.
Verrica is a dermatology therapeutics company developing medications for skin diseases requiring medical interventions. On July 21, 2023, Verrica’s lead product, YCANTH™ (cantharidin), became the first treatment approved by the FDA to treat pediatric and adult patients with molluscum contagiosum, a highly contagious viral skin infection affecting approximately 6 million people in the United States, primarily children. VP-102 is also in development to treat common warts and external genital warts, two of the largest unmet needs in medical dermatology. Verrica is developing VP-103, its second cantharidin-based product candidate, for the treatment of plantar warts. Verrica has also entered a worldwide license agreement with Lytix Biopharma AS to develop and commercialize VP-315 (formerly LTX-315 and VP-LTX-315) for dermatologic oncology conditions. For more information, visit www.verrica.com.
FOR MORE INFORMATION, PLEASE CONTACT:
Chief Financial Officer

Frequently Asked Questions

When is Verrica's next conference call?

Verrica's next conference call is scheduled for May 13, 2024, at 8:30 a.m. ET.

How can I participate in the conference call?

To join the call, dial 1-877-407-4018 domestically or 1-201-689-8471 internationally.

What is YCANTH™ used to treat?

YCANTH™ is the first FDA-approved treatment for molluscum contagiosum.

What other products is Verrica developing?

Verrica is developing VP-102 for warts and VP-103 for plantar warts.

Where can I find the live webcast?

The live webcast can be accessed on Verrica's investor relations website.

Last updated: May 8, 2024