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Verrica Pharmaceuticals

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uuid0002gq1

Namestring
Verrica Pharmaceuticals
Legal namestring
Verrica Pharmaceuticals Inc.
Company typeenum
Public
Founded yearint
2017
Descriptiontext

Verrica Pharmaceuticals Inc. (NASDAQ: VRCA) is a U.S.-headquartered dermatology therapeutics company that develops and commercializes drug-device combination products and immunotherapies for viral skin diseases and non-melanoma skin cancers. Its lead commercial asset is YCANTH (VP-102), a cantharidin-based topical solution paired with a proprietary applicator that in July 2023 became the first and only FDA-approved treatment for molluscum contagiosum in adult and pediatric patients aged two and older. Verrica generates revenue primarily through direct U.S. product sales to dermatologists and pediatricians via a field force scaling from 40 to 50 representatives in 2026, supplemented by transfer-pricing and milestone payments plus future royalties from partner Torii Pharmaceutical, which launched YCANTH in Japan in February 2026 following September 2025 MHLW approval. Beyond the approved indication, Verrica is running a global Phase 3 program (COVE-1/COVE-3) targeting the ~22 million U.S. common-warts population — an indication with no FDA-approved therapy — and is developing VP-315 (ruxotemitide), a lytic-peptide immunotherapy licensed from Lytix Biopharma that showed a 97% objective response rate in Phase 2 basal cell carcinoma studies with potential abscopal effects. The company is also pursuing an EU MAA filing as early as Q4 2026, is publicly listed in West Chester, Pennsylvania with 51–100 employees, and remains EBITDA-negative while investing in commercial scaling, label expansion, and pipeline development funded by a $50 million November 2025 PIPE and a prior $42 million 2024 public offering.

Short descriptiontext

Verrica Pharmaceuticals (NASDAQ: VRCA) is a commercial-stage dermatology therapeutics company that markets YCANTH, the first FDA-approved treatment for molluscum contagiosum, to U.S. dermatologists and pediatricians while expanding into common warts, basal cell carcinoma, Japan, and the EU.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersWest Chester, United States
HQ citystring
West Chester
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
dermatology therapeutics, topical pharmaceuticals, drug-device combination, molluscum treatment, skin disease medications
Industry1 code
1Dermatology Specialty Pharmaceuticals
CodeHLAIACALPrimaryYes
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Dermatology Pharmaceuticals
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1YCANTH Product Sales
TypeHardware Sales
Description

Revenue from direct sales of YCANTH product in the U.S. market. Q1 2026 U.S. product revenue was $4.3 million representing 25.4% year-over-year growth. Full year 2025 YCANTH product revenue was $15.3 million.

tradingview.com
2Milestone Payments from Torii
TypeLicensing Royalties
Description

One-time payments from partner Torii Pharmaceutical upon achievement of development and regulatory milestones. In 2025, Verrica received $18 million in milestone payments from Torii.

tradingview.com
3Transfer Price Revenue (Japan)
TypeHardware Sales
Description

Verrica supplies YCANTH applicators to Torii Pharmaceutical at a transfer price during the manufacturing transfer period, followed by royalties on net sales after manufacturing transfer completion.

investing.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Marketing or Sales, Operations, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Verrica Pharmaceuticals develops and commercializes prescription dermatology therapeutics for skin diseases requiring medical intervention. Its flagship product YCANTH (VP-102) is an FDA-approved drug-device combination topical treatment for molluscum contagiosum in adult and pediatric patients two years and older, with pipeline expansion into common warts. Additional pipeline candidates include VP-315, an investigational immunotherapy for basal cell carcinoma derived from a lytic peptide technology platform, and VP-103.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 25.4% year-over-year growth in U.S. YCANTH product revenue (Q1 2026)
+3 more records
Product overview1 text field

Verrica Pharmaceuticals is a dermatology therapeutics company focused on developing and commercializing medications for skin diseases. The company's portfolio includes FDA-approved YCANTH (VP-102) for molluscum contagiosum, pipeline candidates VP-315 for basal cell carcinoma, and VP-103 for additional dermatological conditions. The company is also expanding YCANTH into common warts treatment through Phase 3 trials. Products include a drug-device combination approach with proprietary formulations and applicators. Verrica operates primarily in the U.S. with international expansion through partnership with Torii Pharmaceutical in Japan.

Product and service3 records
1YCANTH (VP-102)
CategoryDermatology Pharmaceuticals
Description

FDA-approved drug-device combination topical treatment containing a proprietary cantharidin-based formulation with a specialized applicator, indicated for molluscum contagiosum in adult and pediatric patients two years of age and older. The same product is being evaluated in a global Phase 3 program (COVE-3) for common warts, which would make it the first FDA-approved therapy for that indication.

2VP-315 (Ruxotemitide)
CategoryDermatology Pharmaceuticals (pipeline)
Description

Investigational immunotherapy for basal cell carcinoma and non-melanoma skin cancers, derived from a licensed lytic peptide technology platform. Phase 2 data showed a 97% objective response rate with over half of lesions achieving complete histological resolution and evidence of abscopal effects in untreated tumors.

3VP-103
Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-12-01
Description

Development and commercialization partnership for YCANTH in Japan. Torii received Japanese Ministry of Health approval in September 2025 and launched YCANTH in February 2026. Companies share Phase 3 costs 50/50, with Torii funding first $40 million of trial costs. Verrica supplies product at transfer price and receives royalties after manufacturing transfer.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Global Phase 3 program for YCANTH (VP-102) in common warts with cost-sharing arrangement. Torii funding approximately 90% of current trial budget under 50/50 cost-sharing. Verrica retains full commercial rights outside Japan.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Licensing partner for ruxotemitide (VP-315), an investigational immunotherapy derived from Lytix's lytic peptide technology platform. Phase 2 data in basal cell carcinoma presented at SITC. Verrica holds license for dermatologic oncology applications.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Commercial-stage medical dermatology biotech with FDA-approved topical products (e.g., Zoryve) and similar small-cap public profile. Comparable in therapeutic focus on skin diseases, prescriber base (dermatologists/PCPs), and commercial-stage execution challenges.

TypeDirect peer
Description

Clinical and commercial-stage dermatology company developing therapeutics for skin diseases. Similar size, similar dermatology-focused R&D model with both approved and pipeline assets targeting underserved skin conditions.

TypeDirect peer
Description

Dermatology-focused company now part of Organon that developed VTAMA (tapinarof) for psoriasis and atopic dermatitis. Directly comparable medical dermatology peer with similar prescriber base and topical therapeutic approach. Verrica's new CPO came from Dermavant.

TypeBroad incumbent
Description

Established biopharma with Opzelura (ruxolitinib cream), the leading topical JAK inhibitor in atopic dermatitis and vitiligo. Comparable in dermatology commercial infrastructure and prescriber relationships, though Incyte is far larger and broader.

TypeBroad incumbent
Description

Global dermatology pure-play with broad portfolio across prescription, aesthetics, and consumer skincare. Comparable prescriber base and dermatology commercial scale, though much larger and more diversified than Verrica.

TypeDirect peer
Description

Clinical-stage immunology company with dermatology and inflammatory disease focus, partnering assets with larger pharma. Comparable R&D-stage dermatology biotech profile with multiple pipeline candidates.

TypeEmerging player
Description

Smaller dermatology company focused on actinic keratosis and superficial skin cancers. Comparable in dermatology therapeutics and prescriber overlap with dermatologists, though focused on different indications.

TypeBroad incumbent
Description

Large incumbent with EUCRISA (crisaborole) for atopic dermatitis and broader dermatology franchise. Comparable prescriber relationships and infrastructure, though as a broad pharma company with substantially greater resources.

TypeBroad incumbent
Description

Major incumbent in dermatology via Skyrizi and Rinvoq for psoriasis and other inflammatory skin conditions. Comparable prescriber base and dermatology commercial footprint, though with vastly larger resources and portfolio breadth.

TypeBroad incumbent
Description

Global specialty pharma with dermatology portfolio including ILUMYA (tildrakizumab) for psoriasis. Comparable medical dermatology focus and prescriber base, with significantly greater commercial scale globally including India.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds9 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Verrica Pharmaceuticals

Dermatology Pharmaceuticalsverricapharmaceuticals.com

Verrica Pharmaceuticals (NASDAQ: VRCA) is a commercial-stage dermatology therapeutics company that markets YCANTH, the first FDA-approved treatment for molluscum contagiosum, to U.S. dermatologists and pediatricians while expanding into common warts, basal cell carcinoma, Japan, and the EU.

What Verrica Pharmaceuticals does

Verrica Pharmaceuticals Inc. (NASDAQ: VRCA) is a U.S.-headquartered dermatology therapeutics company that develops and commercializes drug-device combination products and immunotherapies for viral skin diseases and non-melanoma skin cancers. Its lead commercial asset is YCANTH (VP-102), a cantharidin-based topical solution paired with a proprietary applicator that in July 2023 became the first and only FDA-approved treatment for molluscum contagiosum in adult and pediatric patients aged two and older. Verrica generates revenue primarily through direct U.S. product sales to dermatologists and pediatricians via a field force scaling from 40 to 50 representatives in 2026, supplemented by transfer-pricing and milestone payments plus future royalties from partner Torii Pharmaceutical, which launched YCANTH in Japan in February 2026 following September 2025 MHLW approval. Beyond the approved indication, Verrica is running a global Phase 3 program (COVE-1/COVE-3) targeting the ~22 million U.S. common-warts population — an indication with no FDA-approved therapy — and is developing VP-315 (ruxotemitide), a lytic-peptide immunotherapy licensed from Lytix Biopharma that showed a 97% objective response rate in Phase 2 basal cell carcinoma studies with potential abscopal effects. The company is also pursuing an EU MAA filing as early as Q4 2026, is publicly listed in West Chester, Pennsylvania with 51–100 employees, and remains EBITDA-negative while investing in commercial scaling, label expansion, and pipeline development funded by a $50 million November 2025 PIPE and a prior $42 million 2024 public offering.

Verrica Pharmaceuticals firmographics

Firmographics
Name
Verrica Pharmaceuticals
Legal name
Verrica Pharmaceuticals Inc.
Website
https://verricapharmaceuticals.com
Company type
Public
Founded year
2017
Operating status
Operating
Headcount range
51–100 employees
Short description
Verrica Pharmaceuticals (NASDAQ: VRCA) is a commercial-stage dermatology therapeutics company that markets YCANTH, the first FDA-approved treatment for molluscum contagiosum, to U.S. dermatologists and pediatricians while expanding into common warts, basal cell carcinoma, Japan, and the EU.
Ownership category
akta.pro rank

Verrica Pharmaceuticals industry classification

Industry
Product category
Dermatology Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Dermatology Specialty Pharmaceuticals (HLAIACAL)

Keywords

  • Dermatology therapeutics
  • Topical pharmaceuticals
  • Drug-device combination
  • Molluscum treatment
  • Skin disease medications

Where Verrica Pharmaceuticals is headquartered

Location

Headquarters

HQ city
West Chester
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Verrica Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Operations, Others

Revenue model

  1. YCANTH Product Sales: Revenue from direct sales of YCANTH product in the U.S. market. Q1 2026 U.S. product revenue was $4.3 million representing 25.4% year-over-year growth. Full year 2025 YCANTH product revenue was $15.3 million.
  2. Milestone Payments from Torii: One-time payments from partner Torii Pharmaceutical upon achievement of development and regulatory milestones. In 2025, Verrica received $18 million in milestone payments from Torii.
  3. Transfer Price Revenue (Japan): Verrica supplies YCANTH applicators to Torii Pharmaceutical at a transfer price during the manufacturing transfer period, followed by royalties on net sales after manufacturing transfer completion.

Go-to-market motion3 records

Distribution channels3 records

Marketing channels5 records

Verrica Pharmaceuticals product offering

Product offering

Core offering

Verrica Pharmaceuticals develops and commercializes prescription dermatology therapeutics for skin diseases requiring medical intervention. Its flagship product YCANTH (VP-102) is an FDA-approved drug-device combination topical treatment for molluscum contagiosum in adult and pediatric patients two years and older, with pipeline expansion into common warts. Additional pipeline candidates include VP-315, an investigational immunotherapy for basal cell carcinoma derived from a lytic peptide technology platform, and VP-103.

Product overview

Verrica Pharmaceuticals is a dermatology therapeutics company focused on developing and commercializing medications for skin diseases. The company's portfolio includes FDA-approved YCANTH (VP-102) for molluscum contagiosum, pipeline candidates VP-315 for basal cell carcinoma, and VP-103 for additional dermatological conditions. The company is also expanding YCANTH into common warts treatment through Phase 3 trials. Products include a drug-device combination approach with proprietary formulations and applicators. Verrica operates primarily in the U.S. with international expansion through partnership with Torii Pharmaceutical in Japan.

Differentiator

Problem solved

Functional benefit

Products and services

  • YCANTH (VP-102) FDA-approved drug-device combination topical treatment containing a proprietary cantharidin-based formulation with a specialized applicator, indicated for molluscum contagiosum in adult and pediatric patients two years of age and older. The same product is being evaluated in a global Phase 3 program (COVE-3) for common warts, which would make it the first FDA-approved therapy for that indication.
  • VP-315 (Ruxotemitide) Investigational immunotherapy for basal cell carcinoma and non-melanoma skin cancers, derived from a licensed lytic peptide technology platform. Phase 2 data showed a 97% objective response rate with over half of lesions achieving complete histological resolution and evidence of abscopal effects in untreated tumors.
  • VP-103

Quantifiable outcome

  • 25.4% year-over-year growth in U.S. YCANTH product revenue (Q1 2026)
  • +3 more outcomes

Companies that use Verrica Pharmaceuticals

Customer profile

Segments4 records

Ideal customer profiles3 records

Verrica Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Verrica Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • Torii PharmaceuticalcoreChannel Partner/ Reseller/ Distributor · 1 December 2025Development and commercialization partnership for YCANTH in Japan. Torii received Japanese Ministry of Health approval in September 2025 and launched YCANTH in February 2026. Companies share Phase 3 costs 50/50, with Torii funding first $40 million of trial costs. Verrica supplies product at transfer price and receives royalties after manufacturing transfer.
  • Torii PharmaceuticalcoreStrategic or Co-development PartnerGlobal Phase 3 program for YCANTH (VP-102) in common warts with cost-sharing arrangement. Torii funding approximately 90% of current trial budget under 50/50 cost-sharing. Verrica retains full commercial rights outside Japan.
  • Lytix BiopharmacoreStrategic or Co-development PartnerLicensing partner for ruxotemitide (VP-315), an investigational immunotherapy derived from Lytix's lytic peptide technology platform. Phase 2 data in basal cell carcinoma presented at SITC. Verrica holds license for dermatologic oncology applications.

Scale indicators8 records

Recent moves6 records

Expansion highlights5 records

Verrica Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Arcutis Biotherapeutics: Commercial-stage medical dermatology biotech with FDA-approved topical products (e.g., Zoryve) and similar small-cap public profile. Comparable in therapeutic focus on skin diseases, prescriber base (dermatologists/PCPs), and commercial-stage execution challenges.
  • Aclaris Therapeutics: Clinical and commercial-stage dermatology company developing therapeutics for skin diseases. Similar size, similar dermatology-focused R&D model with both approved and pipeline assets targeting underserved skin conditions.
  • Dermavant Sciences (Organon): Dermatology-focused company now part of Organon that developed VTAMA (tapinarof) for psoriasis and atopic dermatitis. Directly comparable medical dermatology peer with similar prescriber base and topical therapeutic approach. Verrica's new CPO came from Dermavant.
  • AnaptysBio: Clinical-stage immunology company with dermatology and inflammatory disease focus, partnering assets with larger pharma. Comparable R&D-stage dermatology biotech profile with multiple pipeline candidates.

Broad incumbents

  • Incyte Corporation: Established biopharma with Opzelura (ruxolitinib cream), the leading topical JAK inhibitor in atopic dermatitis and vitiligo. Comparable in dermatology commercial infrastructure and prescriber relationships, though Incyte is far larger and broader.
  • Galderma: Global dermatology pure-play with broad portfolio across prescription, aesthetics, and consumer skincare. Comparable prescriber base and dermatology commercial scale, though much larger and more diversified than Verrica.
  • Pfizer (Dermatology): Large incumbent with EUCRISA (crisaborole) for atopic dermatitis and broader dermatology franchise. Comparable prescriber relationships and infrastructure, though as a broad pharma company with substantially greater resources.
  • AbbVie (Dermatology): Major incumbent in dermatology via Skyrizi and Rinvoq for psoriasis and other inflammatory skin conditions. Comparable prescriber base and dermatology commercial footprint, though with vastly larger resources and portfolio breadth.
  • Sun Pharma (Dermatology): Global specialty pharma with dermatology portfolio including ILUMYA (tildrakizumab) for psoriasis. Comparable medical dermatology focus and prescriber base, with significantly greater commercial scale globally including India.

Emerging players

  • Biofrontera: Smaller dermatology company focused on actinic keratosis and superficial skin cancers. Comparable in dermatology therapeutics and prescriber overlap with dermatologists, though focused on different indications.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Verrica Pharmaceuticals social profiles

Digital presence

Verrica Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Verrica Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles1 record

Verrica Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds9 records

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Verrica Pharmaceuticals M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Verrica Pharmaceuticals

What does Verrica Pharmaceuticals do?

Verrica Pharmaceuticals develops and commercializes prescription dermatology therapeutics for skin diseases requiring medical intervention. Its flagship product YCANTH (VP-102) is an FDA-approved drug-device combination topical treatment for molluscum contagiosum in adult and pediatric patients two years and older, with pipeline expansion into common warts. Additional pipeline candidates include VP-315, an investigational immunotherapy for basal cell carcinoma derived from a lytic peptide technology platform, and VP-103.

Is Verrica Pharmaceuticals a public or private company?

Verrica Pharmaceuticals is a public company. It is classified as public and is currently operating.

When was Verrica Pharmaceuticals founded?

Verrica Pharmaceuticals was founded in 2017. It employs 51 to 100 people.

Where is Verrica Pharmaceuticals based?

Verrica Pharmaceuticals is headquartered in West Chester, United States, in the North America region.

How does Verrica Pharmaceuticals make money?

Three revenue lines are on record. YCANTH Product Sales are the primary driver. The others are milestone Payments from Torii and transfer Price Revenue (Japan).

Who are Verrica Pharmaceuticals's main competitors?

Direct peers on record are Arcutis Biotherapeutics, Aclaris Therapeutics, Dermavant Sciences (Organon) and AnaptysBio. Broad incumbents are Incyte Corporation, Galderma, Pfizer (Dermatology), AbbVie (Dermatology) and Sun Pharma (Dermatology). Biofrontera is listed as an emerging player.

Does Verrica Pharmaceuticals have an API?

No public API is recorded for Verrica Pharmaceuticals.

What industry is Verrica Pharmaceuticals in?

Verrica Pharmaceuticals's product category is Dermatology Pharmaceuticals. Its primary akta.pro industry code is HLAIACAL, Dermatology Specialty Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
American Banking and Market NewsVerrica Pharmaceuticals Inc. (NASDAQ:VRCA) Stock Has Average Target Price of $12.67Verrica Pharmaceuticals shares have a consensus 'Hold' rating with an average 12-month target price of $12.67. Analysts are split, with one sell, one hold, and three buy ratings. Armistice Capital increased its stake by 75.1% in Q4, holding 7% of the company.MarketBeatVerrica Pharmaceuticals Inc. (NASDAQ:VRCA) Stock Has Average Target Price of $12.67Verrica Pharmaceuticals has a consensus 'Hold' rating with an average 12-month target price of $12.67. Wall Street Zen upgraded the stock to 'sell,' Lake Street Capital initiated coverage with a 'buy' and $9.00 target, and Armistice Capital raised its stake by 75.1% in Q4. The company's lead product, YCANTHE, is FDA-approved for molluscum contagiosum.Stock TitanVerrica Phase 3 Analysis: YCANTH Clears Molluscum ~4x FasterVerrica Pharmaceuticals will present pooled Phase 3 data showing YCANTH clears molluscum contagiosum about four times faster than vehicle, with 60.1% complete clearance by Day 84 versus 19.9% with vehicle. The analysis indicates treatment effect independent of disease duration, supporting early intervention.TradingViewVRCA: Phase III programs for common warts and BCC advance rapidly, with strong efficacy and global expansionVRCA highlighted rapid progress in commercializing YCANTH for molluscum and advancing phase III trials for common warts, citing strong efficacy and safety data. VP-315 for basal cell carcinoma is phase III-ready, showing high response rates and expedited regulatory pathways.YahooVerrica Pharmaceuticals to Present YCANTH® and VP-315 Data at Two Upcoming Dermatology ConferencesVerrica Pharmaceuticals will present posters on YCANTH and VP-315 at two September 2026 dermatology conferences. A post-hoc analysis shows YCANTH drove high complete clearance rates in molluscum contagiosum patients regardless of disease duration. VP-315 data from a Phase 2 trial shows primary tumor and abscopal signals.Stock TitanVerrica to Present YCANTH, VP-315 Data at ConferencesVerrica Pharmaceuticals will present YCANTH and VP-315 data at two September 2026 dermatology conferences. YCANTH post-hoc analysis showed 48.9% complete clearance in patients with disease ≤12 months and 58.8% in those >12 months. VP-315 data showed potential abscopal effects in untreated basal cell carcinoma lesions.BioSpaceVerrica Pharmaceuticals to Present YCANTH® and VP-315 Data at Two Upcoming Dermatology ConferencesVerrica Pharmaceuticals will present posters on YCANTH and VP-315 at two September 2026 dermatology conferences. A post-hoc analysis of YCANTH Phase 3 trials showed complete clearance rates of 48.9% and 58.8% regardless of disease duration, while VP-315 showed abscopal-like effects in basal cell carcinoma.Hospital ManagementVerrica completes enrolment in Phase III trial of YcanthVerrica Pharmaceuticals completed enrolment in its Phase III COVE-2 trial of Ycanth (VP-102) for common warts, following a Phase II trial showing wart reduction. The interim analysis recommended no additional subjects, with top-line data expected in Q1 2027. The second trial, COVE-3, has exceeded 50% of its enrolment target.Clinical Trials ArenaVerrica completes enrolment in Phase III trial of YcanthVerrica Pharmaceuticals completed enrolment in its Phase III trial COVE-2 for Ycanth, a treatment for common warts. Top-line data are expected in the first quarter of 2027, and the second trial COVE-3 has exceeded 50% of its enrolment target. The company plans to seek marketing approval in the US and Japan based on these results.Quiver Quantitative$VRCA stock is up 11% today. Here's what we see in our data. | VRCA Stock NewsVRCA shares rose 11% today with roughly $1.73 million in trading volume, according to Polygon data. Insiders made six purchases totaling about $210,888 over six months, while 14 institutional investors added shares and 27 reduced positions in the most recent quarter. Q2 2026 revenue was $5.9 million, down 53.85% year over year.