8.42
+0.94(+12.57%)
Currency In USD
| Previous Close | 7.48 |
| Open | 7.43 |
| Day High | 8.48 |
| Day Low | 7.2 |
| 52-Week High | 12 |
| 52-Week Low | 3.28 |
| Volume | 195,142 |
| Average Volume | 387,009 |
| Market Cap | 79.91M |
| PE | -2.93 |
| EPS | -2.87 |
| Moving Average 50 Days | 4.4 |
| Moving Average 200 Days | 5.47 |
| Change | 0.94 |
If you invested $1000 in Verrica Pharmaceuticals Inc. (VRCA) since IPO date, it would be worth $481.14 as of December 04, 2025 at a share price of $8.42. Whereas If you bought $1000 worth of Verrica Pharmaceuticals Inc. (VRCA) shares 5 years ago, it would be worth $848.79 as of December 04, 2025 at a share price of $8.42.
For more details, use our stock calculator to calculate how much you would've made investing different amounts on specific dates.
Verrica Pharmaceuticals Announces Private Placement Financing of $50 Million to Retire Debt and Extend Cash Runway
GlobeNewswire Inc.
Nov 24, 2025 1:00 PM GMT
Proceeds will fully retire debt facility from OrbiMed and fund company operations, thereby extending expected cash runway into mid-2027Financing anchored by Caligan Partners LP and PBM Capital, along with new and existing investors; Caligan Partners
Verrica Pharmaceuticals Presents New Data on VP-315 from its Phase 2 Clinical Trial in Basal Cell Carcinoma at the 40th Society for Immunotherapy of Cancer Annual Meeting
GlobeNewswire Inc.
Nov 10, 2025 1:00 PM GMT
– Exploratory Phase 2 analysis shows Verrica’s novel oncolytic peptide, VP-315, reprograms the tumor microenvironment, increasing cytotoxic T-cell infiltration and reducing immunosuppressive T-regulatory cells – – Findings provide mechanistic immunol
Verrica Pharmaceuticals Receives Positive Feedback from the European Medicines Agency (EMA) Supporting a Clear Regulatory Path Forward to File for Approval of YCANTH® in the European Union
GlobeNewswire Inc.
Oct 20, 2025 8:05 PM GMT
– EMA concludes that the primary endpoint and supportive secondary endpoints from prior successful Phase 3 studies conducted in the U.S. and Japan are adequate to support a filing for the approval of YCANTH® in the EU and that no additional Phase 3 s