Verrica Pharmaceuticals Reports Fourth Quarter and Full Year 2024 Financial Results
Verrica Pharmaceuticals (VRCA) reported Q4 and full-year 2024 results, highlighting a 12.3% quarterly growth in YCANTH® dispensed applicator units to 8,654 in Q4'24. The company achieved positive quarterly revenue earlier than expected and implemented significant cost reductions, targeting cash-positive monthly operating results by end of 2025.
Q4 2024 financial results showed product revenue of $0.3M (down from $1.9M in Q4 2023), with reduced operating expenses. Full-year 2024 results included product revenue of $6.6M (up from $4.7M in 2023). The company reported a net loss of $76.6M for 2024.
Key developments include: a $42M public offering in November 2024, strengthening the balance sheet; advancement of late-stage pipeline programs in basal cell carcinoma (VP-315) and common warts (VP-102/YCANTH); and introduction of a new single applicator configuration in Q1 2025. The company ended 2024 with $46.3M in cash and cash equivalents.
Verrica Pharmaceuticals (VRCA) ha riportato i risultati del quarto trimestre e dell'intero anno 2024, evidenziando una crescita trimestrale del 12,3% nelle unità di applicatori YCANTH® distribuite, raggiungendo 8.654 nel Q4'24. L'azienda ha ottenuto ricavi trimestrali positivi prima del previsto e ha implementato significative riduzioni dei costi, puntando a risultati operativi mensili positivi in termini di liquidità entro la fine del 2025.
I risultati finanziari del Q4 2024 hanno mostrato ricavi da prodotto pari a 0,3 milioni di dollari (in calo rispetto a 1,9 milioni di dollari nel Q4 2023), con spese operative ridotte. I risultati dell'intero anno 2024 hanno incluso ricavi da prodotto di 6,6 milioni di dollari (in aumento rispetto a 4,7 milioni di dollari nel 2023). L'azienda ha riportato una perdita netta di 76,6 milioni di dollari per il 2024.
Sviluppi chiave includono: un'offerta pubblica di 42 milioni di dollari a novembre 2024, che rafforza il bilancio; il progresso dei programmi in fase avanzata nella carcinoma a cellule basocellulari (VP-315) e nei comuni verruche (VP-102/YCANTH); e l'introduzione di una nuova configurazione di applicatore singolo nel Q1 2025. L'azienda ha chiuso il 2024 con 46,3 milioni di dollari in contante e equivalenti di contante.
Verrica Pharmaceuticals (VRCA) informó los resultados del cuarto trimestre y del año completo 2024, destacando un crecimiento trimestral del 12.3% en las unidades de aplicadores YCANTH® dispensadas, alcanzando 8,654 en el Q4'24. La compañía logró ingresos trimestrales positivos antes de lo esperado e implementó reducciones de costos significativas, con el objetivo de obtener resultados operativos mensuales positivos en efectivo para finales de 2025.
Los resultados financieros del Q4 2024 mostraron ingresos por productos de $0.3M (a la baja desde $1.9M en el Q4 2023), con gastos operativos reducidos. Los resultados del año completo 2024 incluyeron ingresos por productos de $6.6M (aumento desde $4.7M en 2023). La compañía reportó una pérdida neta de $76.6M para 2024.
Los desarrollos clave incluyen: una oferta pública de $42M en noviembre de 2024, fortaleciendo el balance; el avance de programas en etapa avanzada en carcinoma de células basocelulares (VP-315) y verrugas comunes (VP-102/YCANTH); y la introducción de una nueva configuración de aplicador único en el Q1 2025. La compañía cerró 2024 con $46.3M en efectivo y equivalentes de efectivo.
베리카 제약(VRCA)는 2024년 4분기 및 연간 실적을 보고하며, Q4'24에서 YCANTH® 분배 적용기 유닛이 12.3% 성장하여 8,654개에 도달했다고 강조했습니다. 회사는 예상보다 빠르게 긍정적인 분기 매출을 달성하고, 2025년 말까지 현금 흐름이 긍정적인 월 운영 결과를 목표로 주요 비용 절감을 시행했습니다.
2024년 4분기 재무 결과는 제품 매출이 30만 달러(2023년 4분기 190만 달러에서 감소)였으며, 운영 비용이 감소했습니다. 2024년 전체 연간 결과는 제품 매출이 660만 달러(2023년 470만 달러에서 증가)로 포함되었습니다. 회사는 2024년에 7660만 달러의 순손실을 보고했습니다.
주요 개발 사항으로는: 2024년 11월에 4200만 달러의 공모가 있으며, 재무 상태를 강화했습니다; 기저 세포 암종(VP-315) 및 일반 사마귀(VP-102/YCANTH)에서의 후기 단계 파이프라인 프로그램의 진전; 2025년 1분기에 새로운 단일 적용기 구성을 도입했습니다. 회사는 2024년 말에 4630만 달러의 현금 및 현금성 자산을 보유하고 종료했습니다.
Verrica Pharmaceuticals (VRCA) a publié les résultats du quatrième trimestre et de l'année entière 2024, mettant en avant une croissance trimestrielle de 12,3 % des unités d'applicateurs YCANTH® distribuées, atteignant 8 654 au T4'24. L'entreprise a réalisé des revenus trimestriels positifs plus tôt que prévu et a mis en œuvre des réductions de coûts significatives, visant des résultats d'exploitation mensuels positifs en espèces d'ici la fin 2025.
Les résultats financiers du T4 2024 ont montré des revenus produits de 0,3 million de dollars (en baisse par rapport à 1,9 million de dollars au T4 2023), avec des dépenses d'exploitation réduites. Les résultats de l'année entière 2024 comprenaient des revenus produits de 6,6 millions de dollars (en hausse par rapport à 4,7 millions de dollars en 2023). L'entreprise a déclaré une perte nette de 76,6 millions de dollars pour 2024.
Les développements clés incluent : une offre publique de 42 millions de dollars en novembre 2024, renforçant le bilan ; l'avancement des programmes en phase avancée dans le carcinome basocellulaire (VP-315) et les verrues communes (VP-102/YCANTH) ; et l'introduction d'une nouvelle configuration d'applicateur unique au T1 2025. L'entreprise a terminé 2024 avec 46,3 millions de dollars en liquidités et équivalents de liquidités.
Verrica Pharmaceuticals (VRCA) hat die Ergebnisse des vierten Quartals und des gesamten Jahres 2024 bekannt gegeben und dabei ein vierteljährliches Wachstum von 12,3 % bei den ausgegebenen Einheiten des YCANTH®-Applikators auf 8.654 im Q4'24 hervorgehoben. Das Unternehmen erzielte früher als erwartet positive vierteljährliche Einnahmen und implementierte erhebliche Kostensenkungen, mit dem Ziel, bis Ende 2025 monatlich positive Betriebsergebnisse zu erzielen.
Die finanziellen Ergebnisse für Q4 2024 zeigten Produktumsätze von 0,3 Millionen USD (ein Rückgang von 1,9 Millionen USD im Q4 2023), bei reduzierten Betriebskosten. Die Ergebnisse des gesamten Jahres 2024 umfassten Produktumsätze von 6,6 Millionen USD (ein Anstieg von 4,7 Millionen USD im Jahr 2023). Das Unternehmen berichtete für 2024 einen Nettoverlust von 76,6 Millionen USD.
Wichtige Entwicklungen umfassen: ein öffentliches Angebot über 42 Millionen USD im November 2024, das die Bilanz stärkt; den Fortschritt bei späten Pipeline-Programmen bei Basalzellkarzinom (VP-315) und gewöhnlichen Warzen (VP-102/YCANTH); sowie die Einführung einer neuen Einzelapplikator-Konfiguration im Q1 2025. Das Unternehmen schloss 2024 mit 46,3 Millionen USD an Bargeld und liquiden Mitteln ab.
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Insights
Verrica's Q4 and full-year 2024 results reveal a company in transition with encouraging operational improvements but persistent financial challenges. The 12.3% sequential growth in YCANTH dispensed applicator units demonstrates early traction for their restructured commercial strategy, though Q4 product revenue dropped to
The company has made substantial progress reducing its cash burn, cutting operating expenses by approximately
However, Verrica's financial position remains precarious. Despite raising
The pipeline shows promise with their VP-315 candidate for basal cell carcinoma demonstrating a
Verrica's clinical data for VP-315 in basal cell carcinoma represents a potentially significant advancement in dermatological oncology. The
The company's pipeline strategy logically leverages their existing commercial infrastructure by exploring label expansion for YCANTH (VP-102) into common warts. Their partnership with Torii Pharmaceutical creates a capital-efficient development path, with Torii providing initial funding for the global Phase 3 program while Verrica defers its portion of costs against future milestones and royalties. This arrangement preserves capital while maintaining significant upside potential.
The Japanese NDA submission for VP-102 by Torii represents another potential value inflection point. With Phase 3 initiation in common warts potentially beginning mid-2025, the
From a product perspective, the introduction of a single applicator configuration for YCANTH represents a strategic move to increase physician adoption by reducing acquisition costs and expanding patient access. This packaging innovation, combined with their targeted commercial approach focusing on high-prevalence territories, demonstrates an intelligent, resource-conscious commercial strategy that may accelerate the product's path to profitability.
– Company generated quarterly sequential growth in YCANTH® dispensed applicator units of
– Company reports positive quarterly revenue earlier than previously disclosed expectations, as new demand resulted in Company’s primary distribution partner ordering applicators of YCANTH during Q4’24 –
– Late-stage pipeline continues to advance with programs in basal cell carcinoma (VP-315) and common warts (VP-102/YCANTH) –
– Recently strengthened balance sheet with the November 2024
– Conference call scheduled for today at 4:30 pm ET –
WEST CHESTER, Pa., March 11, 2025 (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 financial results for the fourth quarter and full year ended December 31, 2024.
“The fourth quarter began a transition period for our company, and we have already achieved several substantial milestones. We completed our commercial strategy realignment, which generated promising sequential growth of dispensed applicator units of YCANTH while simultaneously implementing significant cost reductions across the organization. We also continued advancing our late-stage clinical programs in basal cell carcinoma and common warts,” said Dr. Jayson Rieger, PhD, MBA, President and Chief Executive Officer of Verrica. Rieger continued “We successfully raised equity capital in the fourth quarter to strengthen our balance sheet and allow us to remain focused on commercial execution and development of our clinical assets.”
“Based on achieving these early milestones, I believe Verrica is now on track to successfully execute our turnaround strategy. Our goal is to generate cash positive monthly operating results by the end of 2025. To achieve this, our focus will remain to establish YCANTH as the standard of care for the treatment of molluscum contagiosum. In parallel, we will work to create significant additional value by advancing our late-stage pipeline. We recently reported positive data from our Phase 2 study of our oncolytic peptide candidate, VP-315, for the treatment of basal cell carcinoma, and we also anticipate advancing VP-102 (YCANTH) into a Phase 3 clinical trial for the treatment of common warts as early as mid-2025. With a leaner and more capital-efficient operating model now in place, I believe 2025 is shaping up to become an important year for Verrica as we seek to address the most significant unmet needs in dermatology.”
Conference Call and Webcast Information
The Company will host a conference call today, Tuesday, March 11, 2025, at 4:30 PM, Eastern Time, to discuss its fourth quarter and year-end 2024 financial results and provide a business update. To participate in the conference call, please utilize the following information:
Domestic Dial-In Number: Toll-Free: 1-800-445-7795
International Dial-In Number: 1-785-424-1699
Conference ID: VERRICA
Webcast:
https://viavid.webcasts.com/starthere.jsp?ei=1706610&tp_key=fb81085fc6
Participants can use Guest dial-in #s above and be answered by an operator.
The call will also be broadcast live over the Web and can be accessed on Verrica Pharmaceuticals’ website: www.verrica.com or directly at
https://viavid.webcasts.com/starthere.jsp?ei=1706610&tp_key=fb81085fc6
The conference call will also be available for replay for one month on the Company’s website in the Events Calendar of the Investors section.
Business Highlights and Recent Developments
CORPORATE
- In December 2024, the Company announced a business and operational update outlining the significant progress being made with respect to the new commercial strategy for YCANTH®, Verrica’s product for the treatment of molluscum contagiosum (“molluscum”).
- YCANTH dispensed applicator units in the fourth quarter of 2024 were 8,654 versus the third quarter of 2024 of 7,706, which represents sequential quarterly growth of
12.3% . - The Company has normalized YCANTH distributor inventory levels to meet demand.
- Verrica introduced a new single applicator configuration for YCANTH that became available in the first quarter of 2025 to help meet growing product demand, reduce acquisition costs for physician practices and expand distribution and patient access.
- Verrica continued to advance pipeline of product candidates in common warts and basal cell carcinoma.
- YCANTH dispensed applicator units in the fourth quarter of 2024 were 8,654 versus the third quarter of 2024 of 7,706, which represents sequential quarterly growth of
- In November 2024, the Company announced the pricing of
$42 million public offering of common stock, pre-funded warrants and accompanying Series A and B warrants. - In November 2024, the Company announced the appointments of Dr. Jayson Rieger as President and Chief Executive Officer and as a director, and John Kirby as interim Chief Financial Officer.
- In October 2024, the Company announced a restructuring of its commercial operations to reduce expenses and optimize the efficiency of its field force by reducing the number of sales territories and focusing on those territories that have historically shown a high prevalence of molluscum, a critical mass of previous cantharidin users and strong insurance coverage for YCANTH. The Company also announced that it would reduce headcount in certain support functions to focus on its new commercial strategy. Total operating expenses after the restructuring are expected to be reduced by approximately fifty percent. The Company incurred a one-time charge related to the restructuring of approximately
$1.0 million .
YCANTH® (VP-102)
- In December 2024, the Company announced that its development and commercialization partner, Torii Pharmaceutical Co. Ltd. (“Torii”), submitted a New Drug Application of TO-208 (referred to as VP-102 and marketed as YCANTH® in the U.S.) for the treatment of molluscum in Japan.
- Torii and Verrica are finalizing plans for a co-sponsored global Phase 3 clinical program to develop VP-102 (YCANTH) for the treatment of common warts, with Torii providing all initial funding and Verrica paying its portion of trial costs out of future milestones and royalties. Under the terms of the Torii collaboration and license agreement, Torii will make a milestone payment of
$8 million to Verrica upon initiation of the Phase 3 clinical trial. Initiation of this global study in common warts could begin as early as mid-2025.
VP-315
- In November 2024, the Company disclosed additional data on VP-315 from a post-hoc analysis of the data from Part 2 of the Phase 2 study of VP-315 for the treatment of basal cell carcinoma, and the results were formally presented in January 2025 at the 2025 Winter Clinical Dermatology Conference. Part 2 of the Phase 2 study was designed to explore dosing regimens to help identify the recommended regimen for a Phase 3 clinical study. The analysis of Part 2 of the Phase 2 study demonstrated that treatment with VP-315 led to a calculated objective response rate, or ORR, of
97% , which was defined as the percentage of study subjects who do not demonstrate disease progression and who experience at least a30% reduction in tumor size along with partial or complete response following treatment. - In October 2024, the Company presented two posters at the 2024 Fall Clinical Dermatology Conference featuring positive preliminary topline results from Part 2 of the Phase 2 study. The posters included safety and histologic clearance data from 82 patients with up to 2 target basal cell carcinoma tumors. Preliminary topline results showed that approximately
51% of tumors treated with VP-315 achieved complete histological clearance, while those patients with a residual tumor achieved, on average, approximately71% reduction in tumor size. VP-315 was also well tolerated. No treatment related serious adverse events were reported in the study, and most treatment related adverse events were mild to moderate. - The Company expects to report genomic and immune response data from the Phase 2 trial and to receive minutes from an end-of-phase 2 meeting in the first half of 2025, which will help determine the next steps for the advancement of the program into Phase 3 trials.
Financial Results
Fourth Quarter 2024 Financial Results
- Verrica recognized product revenue of
$0.3 million in the three months ended December 31, 2024 compared to$1.9 million for the same period in 2023. The decrease is due to demand for YCANTH (VP-102) dispensed applicator units being met during fourth quarter of 2024 by existing inventory held by distributors. - Costs of product revenue were
$0.6 million for the three months ended December 31, 2024, compared to$0.1 million for the three months ended December 31, 2023. The increase was partially due to an obsolete inventory write-off of$0.3 million during the three months ended December 31, 2024. - Selling, general and administrative expenses were
$10.0 million in the three months ended December 31, 2024, compared to$17.0 million for the same period in 2023. The decrease of$7.0 million was primarily due to reduction in headcount related costs of$3.7 million , a result of a restructure at the beginning of the period and decrease in advertising and sponsorship costs of$3.6 million . - Research and development expenses were
$1.2 million in the three months ended December 31, 2024, compared to$5.3 million for the same period in 2023. The decrease of$4.1 million was primarily related to a decrease in VP-315 clinical trial costs of$2.1 million , a decrease in headcount related costs of$1.2 million and a reduction of regulatory costs of$0.7 million . - For the three months ended December 31, 2024, net loss was
$16.2 million , or$0.24 per share, compared to a net loss of$24.6 million , or$0.53 per share, for the same period in 2023.
Full Year 2024 Financial Results
- Verrica recognized product revenue of
$6.6 million in the year ended December 31, 2024, compared to$4.7 million for the year ended December 31, 2023. The increase of$1.9 million related to additional sales of YCANTH (VP-102) partially offset by a returns reserve of$3.2 million for estimated returns from certain distributors. The Company determined it was more than probable that product held by certain distributors will be returned based on lower than forecasted sell-through and expiration of product. This increase in reserve was partially offset by a decrease of other gross to net reserves of$1.2 million mostly related to a decrease in co-pay reserve. - Verrica recognized collaboration revenues of
$1.0 million for the year ended December 31, 2024, compared to$0.5 million for the year ended December 31, 2023, each related to supplies and development activity provided to Torii as needed pursuant to the Torii Clinical Supply Agreement. - Costs of product revenue were
$1.9 million for the year ended December 31, 2024, compared to$0.3 million for the year ended December 31, 2023. The increase in product costs of$1.6 million was primarily related to higher sales of YCANTH (VP-102) coupled with obsolete inventory of$0.9 million during the year ended December 31, 2024. - Costs of collaboration revenue were
$0.9 million for the year ended December 31, 2024, compared to$0.5 million for the year ended December 31, 2023. The increase was primarily due to increased manufacturing supply required to support development and testing services pursuant to the Torii Clinical Supply Agreement. - Selling, general and administrative expenses were
$58.8 million for the year ended December 31, 2024, compared to$47.3 million for the year ended December 31, 2023. The increase of$11.5 million was primarily a result of higher expenses related to commercial activities for YCANTH (VP-102) for the treatment of molluscum, including increased compensation, recruiting fees, benefits and travel due to ramp-up of sales force of$8.5 million , as well as increased commercial-related costs of$5.1 million , increased severance costs of$1.8 million due to termination of employees, increased professional services including legal of$4.4 million , and the Dormer legal settlement payment of$0.8 million partially offset by decreased stock compensation expense of$6.8 million related to vesting of restricted stock units and decrease in marketing and sponsorship costs of$2.2 million . - Research and development expenses were
$11.8 million for the year ended December 31, 2024, compared to$20.3 million for the year ended December 31, 2023. The decrease of$8.5 million was primarily attributable to reductions of costs related to YCANTH (VP-102) pre-approval activity of$3.8 million , decreased clinical costs for VP-315 of$3.1 million , decreased stock compensation expense of$0.6 million related to vesting of restricted stock units upon FDA approval and reduction in headcount related costs of$0.7 million , partially offset by increased costs for the development of VP-102 for common warts of$0.5 million . - Interest income was
$1.4 million for the year ended December 31, 2024, compared to$2.7 million for the year ended December 31, 2023. The decrease of$1.3 million was primarily due to a lower cash balance and lower interest rates. - Interest expense was
$9.4 million for the year ended December 31, 2024, compared to$4.0 million for the year ended December 31, 2023. The higher interest expense of$5.4 million was due to Verrica initially borrowing funds pursuant to the OrbiMed credit facility in July 2023. - Change in fair value of derivative liability was
$2.6 million for the year ended December 31, 2024. The OrbiMed Credit Agreement contains a bifurcated settlement feature classified as a derivative liability which is remeasured each accounting period. For the year ended December 31, 2023, the settlement feature was deemed to have no value as the Company did not deem it probable that the repayment of the debt would be accelerated. As a result of the Company failing to meet the revenue threshold specified in the OrbiMed Credit Agreement as of December 31, 2024, the initiation of principal payments beginning in 2025 was triggered. As of December 31, 2024, the embedded derivatives were valued at$2.6 million . - For the year ended December 31, 2024, net loss on a GAAP basis was
$76.6 million , or$1.48 per share, compared to a net loss of$67.0 million , or$1.48 per share, for the year ended December 31, 2023. - For the year ended December 31, 2024, non-GAAP net loss was
$64.6 million , or$1.25 per share, compared to a non-GAAP net loss of$51.8 million , or$1.14 per share, for the year ended December 31, 2023. - As of December 31, 2024, Verrica had cash and cash equivalents of
$46.3 million . Under GAAP, the cash and cash equivalents as of December 31, 2024, would not be sufficient to fund operations for the one-year period following the release of Verrica’s 2024 financial statements. However, should Verrica receive the$8 million milestone payment from Torii (triggered by the initiation of the Phase 3 clinical trial in Japan for common warts) or a portion of the$25 million in proceeds from the exercise of the Series A warrants (issued as part of our November 2024 equity financing with an exercise price of$1.06 80 per share and expiring in November 2025), Verrica could have sufficient cash to fund operations for such period.
Non-GAAP Financial Measures
In evaluating the operating performance of its business, Verrica’s management considers non-GAAP loss from operations, non-GAAP net loss and non-GAAP net loss per share. These non-GAAP financial measures exclude stock-based compensation expense and non-cash interest expense that are required by GAAP. Verrica excludes non-cash stock-based compensation expense from these non-GAAP measures to facilitate comparison to peer companies who also provide similar non-GAAP disclosures and because it reflects how management internally manages the business. In addition, Verrica excludes non-cash interest expense from these non-GAAP measures to facilitate an understanding of the effects of the debt service obligations on the Company’s liquidity and comparisons to peer group companies who also provide similar non-GAAP disclosures and because it is reflective of how management internally manages the business. Non-GAAP loss from operations, non-GAAP net loss and non-GAAP net loss per share should be considered in addition to results prepared in accordance with GAAP, but should not be considered a substitute for, or superior to, GAAP results. Non-GAAP loss from operations, non-GAAP net loss and non-GAAP net loss per share have been reconciled to the nearest GAAP measure in the tables following the financial statements in this press release.
About YCANTH® (VP-102)
YCANTH® is a proprietary drug-device combination product that contains a GMP-controlled formulation of cantharidin delivered via a single-use applicator that allows for precise topical dosing and targeted administration for the treatment of molluscum. YCANTH® is the first and only commercially available product approved by the FDA to treat adult and pediatric patients two years of age and older with molluscum contagiosum — a common, highly contagious skin disease that affects an estimated six million people in the United States, primarily children. Approval of YCANTH® was based upon the positive results from two Phase 3 clinical trials in approximately 500 patients which demonstrated that YCANTH® was a safe and effective therapeutic for the treatment of molluscum. Approximately 225 million lives are eligible to receive YCANTH® covered by insurance. YCANTH® is available to all patients with and without insurance coverage for
About Verrica Pharmaceuticals Inc.
Verrica is a dermatology therapeutics company developing medications for skin diseases requiring medical interventions. Verrica’s product YCANTH® (VP-102) (cantharidin), is the first and only commercially available treatment approved by the FDA to treat adult and pediatric patients two years of age and older with molluscum contagiosum, a highly contagious viral skin infection affecting approximately 6 million people in the United States, primarily children. YCANTH® (VP-102) is also in development to treat common warts, the largest remaining unmet need in medical dermatology. 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 non-melanoma skin cancers including basal cell carcinoma and squamous cell carcinoma. For more information, visit www.verrica.com.
Forward-Looking Statements
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as “believe,” “expect,” “may,” “plan,” “potential,” “will,” and similar expressions, and are based on Verrica’s current beliefs and expectations. These forward-looking statements include statements about the commercialization of YCANTH, cost management initiatives and preservation of capital resources, Verrica’s ability to generate cash positive monthly operating results by the end of 2025, the potential receipt of a milestone payment from Torii, the potential exercise of Series A warrants and receipt of proceeds therefrom, and the clinical development and benefits of Verrica’s product candidates, including YCANTH (VP-102) and VP-315. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include risks and uncertainties related to market conditions, satisfaction of customary closing conditions related to the proposed public offering and other risks and uncertainties that are described in Verrica’s Annual Report on Form 10-K for the year ended December 31, 2024 and other filings Verrica makes with the SEC. Any forward-looking statements speak only as of the date of this press release and are based on information available to Verrica as of the date of this release, and Verrica assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise.
| VERRICA PHARMACEUTICALS INC. | |||||||
| Statements of Operations | |||||||
| (in thousands except share and per share data) | |||||||
| (unaudited) | |||||||
| Three Months Ended December 31, | |||||||
| 2024 | 2023 | ||||||
| Product revenue, net | $ | 315 | $ | 1,866 | |||
| Collaboration revenue | 29 | 122 | |||||
| Total revenue | 344 | 1,988 | |||||
| Operating expenses: | |||||||
| Cost of product revenue | 596 | 145 | |||||
| Cost of collaboration revenue | 29 | 128 | |||||
| Selling, general and admin. | 10,019 | 16,994 | |||||
| Research and development | 1,168 | 5,320 | |||||
| Loss on disposal of assets | (58 | ) | 2,537 | ||||
| Total operating expenses | 11,754 | 25,124 | |||||
| Loss from operations | (11,410 | ) | (23,136 | ) | |||
| Interest income | 205 | 792 | |||||
| Interest expense | (2,349 | ) | (2,306 | ) | |||
| Change in fair value of derivative liability | (2,648 | ) | - | ||||
| Other expense | - | 36 | |||||
| Net loss | $ | (16,202 | ) | $ | (24,614 | ) | |
| Net loss per share, basic and diluted | $ | (0.24 | ) | $ | (0.53 | ) | |
| Weighted-average common shares outstanding, basic and diluted | 67,325,994 | 46,311,454 | |||||
| VERRICA PHARMACEUTICALS INC. | |||||||
| Statements of Operations | |||||||
| (in thousands except share and per share data) | |||||||
| Year Ended December 31, | |||||||
| 2024 | 2023 | ||||||
| Product revenue, net | $ | 6,574 | $ | 4,658 | |||
| Collaboration revenue | 992 | 466 | |||||
| Total revenue | 7,566 | 5,124 | |||||
| Operating expenses: | |||||||
| Cost of product revenue | 1,853 | 289 | |||||
| Cost of collaboration revenue | 887 | 457 | |||||
| Selling, general and administrative | 58,822 | 47,305 | |||||
| Research and development | 11,840 | 20,295 | |||||
| Loss on disposal of assets | 83 | 2,537 | |||||
| Total operating expenses | 73,485 | 70,883 | |||||
| Loss from operations | (65,919 | ) | (65,759 | ) | |||
| Interest income | 1,417 | 2,740 | |||||
| Interest expense | (9,412 | ) | (3,962 | ) | |||
| Change in fair value of derivative liability | (2,648 | ) | - | ||||
| Other expense | (17 | ) | (14 | ) | |||
| Net loss | $ | (76,579 | ) | $ | (66,995 | ) | |
| Net loss per share, basic and diluted | $ | (1.48 | ) | $ | (1.48 | ) | |
| Weighted-average common shares outstanding, basic and diluted | 51,808,228 | 45,342,451 | |||||
| VERRICA PHARMACEUTICALS INC. | ||||||
| Selected Balance Sheet Data | ||||||
| (in thousands) | ||||||
| December 31, 2024 | December 31, 2023 | |||||
| Cash and cash equivalents | $ | 46,329 | $ | 69,547 | ||
| Accts rec., prepaid expenses and inventory | 4,850 | 7,983 | ||||
| Total current assets | 51,179 | 77,530 | ||||
| PP&E, lease right of use asset, other | 2,955 | 4,067 | ||||
| Total assets | $ | 54,134 | $ | 81,597 | ||
| Total liabilities | $ | 63,994 | $ | 61,834 | ||
| Total stockholders' equity | (9,860 | ) | 19,763 | |||
| Total liabilities and stockholders’ equity | $ | 54,134 | $ | 81,597 | ||
| VERRICA PHARMACEUTICALS INC. | |||||||||||
| Reconciliation of Non-GAAP Financial Measures (unaudited) | |||||||||||
| (in thousands except per share data) | |||||||||||
| Three Months Ended December 31, 2024 | |||||||||||
| Loss from operations | Net loss | Net loss per share | |||||||||
| GAAP | $ | (11,410 | ) | $ | (16,202 | ) | $ | (0.24 | ) | ||
| Non-GAAP Adjustments: | |||||||||||
| Stock-based compensation – | |||||||||||
| Selling, general and admin (a) | 378 | 378 | |||||||||
| Stock-based compensation – | |||||||||||
| Research and development (a) | 378 | 378 | |||||||||
| Derivative liability change in value | - | 2,648 | |||||||||
| Non-cash interest expense (b) | - | 616 | |||||||||
| Adjusted | $ | (10,654 | ) | $ | (12,182 | ) | $ | (0.18 | ) | ||
| Three Months December 31, 2023 | |||||||||||
| Loss from operations | Net loss | Net loss per share | |||||||||
| GAAP | $ | (23,136 | ) | $ | (24,614 | ) | $ | (0.53 | ) | ||
| Non-GAAP Adjustments: | |||||||||||
| Stock-based compensation – | |||||||||||
| Selling, general & admin (a) | 1,573 | 1,573 | |||||||||
| Stock-based compensation – | |||||||||||
| Research & development (a) | 502 | 502 | |||||||||
| Non-cash interest expense (b) | - | 473 | |||||||||
| Adjusted | $ | (21,061 | ) | $ | (22,066 | ) | $ | (0.48 | ) | ||
| Year Ended December 31, 2024 | |||||||||||
| Loss from operations | Net loss | Net loss per share | |||||||||
| GAAP | $ | (65,919 | ) | $ | (76,579 | ) | $ | (1.48 | ) | ||
| Non-GAAP Adjustments: | |||||||||||
| Stock-based compensation – | |||||||||||
| Selling, general and admin (a) | 5,219 | 5,219 | |||||||||
| Stock-based compensation – | |||||||||||
| Research and development (a) | 1,945 | 1,945 | |||||||||
| Derivative liability change in value | - | 2,648 | |||||||||
| Non-cash interest expense (b) | - | 2,187 | |||||||||
| Adjusted | $ | (58,755 | ) | $ | (64,580 | ) | $ | (1.25 | ) | ||
| Year Ended December 31, 2023 | |||||||||||
| Loss from operations | Net loss | Net loss per share | |||||||||
| GAAP | $ | (65,759 | ) | $ | (66,995 | ) | $ | (1.48 | ) | ||
| Non-GAAP Adjustments: | |||||||||||
| Stock-based compensation – | |||||||||||
| Selling, general & admin (a) | 11,796 | 11,796 | |||||||||
| Stock-based compensation – | |||||||||||
| Research & development (a) | 2,580 | 2,580 | |||||||||
| Non-cash interest expense (b) | - | 810 | |||||||||
| Adjusted | $ | (51,383 | ) | $ | (51,809 | ) | $ | (1.14 | ) | ||
| (a) | The effects of non-cash stock-based compensation are excluded because of varying available valuation methodologies and subjective assumptions. Verrica believes this is a useful measure for investors because such exclusion facilitates comparison to peer companies who also provide similar non-GAAP disclosures and is reflective of how management internally manages the business. |
| (b) | The effects of non-cash interest charges are excluded because Verrica believes such exclusion facilitates an understanding of the effects of the debt service obligations on the Company’s liquidity and comparisons to peer group companies and is reflective of how management internally manages the business. |
FOR MORE INFORMATION, PLEASE CONTACT:
Investors:
John J Kirby
Interim Chief Financial Officer
jkirby@verrica.com
Kevin Gardner
LifeSci Advisors
kgardner@lifesciadvisors.com
FAQ
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