Kranthi Gorlamari v. Verrica Pharmaceuticals, Inc. et al.

District Court, E.D. Pennsylvania·Decided March 4, 2026·No. 2:22-cv-02226·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF PENNSYLVANIA

KRANTHI GORLAMARI, ; Plaintiff, : v. CIVIL NO. 22-2226 VERRICA PHARMACEUTICALS, INC. et : al., : Defendants. :

Scott, J. March 4, 2026

MEMORANDUM

Plaintiff Kranthi Gorlamari, on behalf of himself and all others similarly situated, claims that Defendants Verrica Pharmaceuticals, Inc. (“Verrica”) and then-CEO Ted White (collectively, “Defendants”) violated Sections 10(b) and 20(a) of the Securities Exchange Act of 1934, and SEC Rule 10b-5 promulgated thereunder, by misleading investors about the likelihood of FDA approval concerning YCANTH, a drug that treats a contagious viral skin infection known as molluscum contagiosum. Plaintiff seeks to certify a class of investors that were likewise misled by Verrica’s alleged misstatements and omissions. Defendants oppose the motion, arguing for similar reasons that Plaintiff is not entitled to the Basic presumption of reliance and that the class definition effectively includes class members who could not have been harmed. Plaintiff submitted the Motion for Class Certification along with the expert report of Dr. Zahn Bozanic on June 13, 2025. ECF Nos. 69, 69-1, and 69-3. Defendants submitted their

Response in Opposition on July 31, 2025. ECF No. 71. Plaintiff filed his Reply on September 12, 2025. ECF No. 73. The Court held oral argument on December 2, 2025.! For reasons given below, the Court grants Plaintiff's motion to certify the class after a modification to the proposed Class Definition. I. Background Verrica Pharmaceuticals, Inc. is a dermatology therapeutics company whose lead product, commercialized as YCANTH and referred to as VP-102 by the Parties, is used to treat a skin infection common in children known as molluscum contagiosum. Second Amended Complaint, ECF No. 40, § 30 (hereinafter “SAC”). Verrica sought and ultimately obtained approval by the U.S. Food and Drug Administration (“FDA”) for the marketing of YCANTH. /d. § 33. But the path to FDA approval was fraught with obstacles. Verrica submitted its first New Drug Application (“NDA”) to the FDA in September 2019. Jd. § 61. By July 2020, the FDA issued a Complete Response Letter (“CRL’’) to Verrica, which indicated that Verrica’s NDA will not be approved until certain conditions are met. /d. § 62. Verrica resubmitted the NDA for VP- 102 in December 2020. /d. ¥ 64 As the resubmitted NDA was under review by the FDA, then-CEO of Verrica, Defendant Ted White, told analysts and prospective investors at RBC Capital Markets Global Healthcare Conference on May 19, 2021 that Verrica was confident that the prior hiccups that resulted in a CRL—concerns about the safety of the container through which patients would self-administer VP-102 and about the status of two facilities where Verrica contracted to make VP-102, namely Sterling Pharmaceutical Services, LLC (“Sterling”) and PPS—would not impede the progress of

Tt is a lamentable rarity for the Court to decide a motion where the quality of briefing and the quality of oral argument are both top notch. It is, however, to the Court’s good fortune to have encountered both excellent briefing and excellent oral argument in this matter. The Court commends Counsel for Plaintiff and Counsel for Defendants for their skillful work on this case.

the resubmitted NDA. /d. § 107. Specifically, Defendant White stated that “we fully anticipate that we’ll have our inspections take place according to plan, and we have not been notified otherwise.” /d. Then, on June 2, 2021, during the Jefferies 2021 Virtual Healthcare Conference, Defendant White stated in relevant part that ‘““our new PDUFA [Prescription Drug User Fee Act] goal date is September 23 to give the agency more time to review data and complete one inspection at one of our facilities.” Jd. § 110. On September 17, 2021, Verrica received a second CRL from the FDA concerning the VP- 102 NDA. Jd. § 70. On September 20, 2021, Verrica informed the market about this CRL, explaining that “the FDA has identified deficiencies at a facility of a contract manufacturing organization [1.e., Sterling], which are not specifically related to the manufacturing of VP-102 but instead raise general quality issues at the facility.” Jd. On September 21, 2021, Verrica’s share price fell 8.3%. Id. § 72. On November 29, 2021, Verrica announced that it had resubmitted once again the VP-102 NDA. /d. 477. On March 2, 2022, Verrica indicated on its SEC Form 10-K that this resubmission had “addressed the successful resolution of inspection deficiencies identified at the CMO [L.e. Sterling] in the CRL.” Jd. 9112. Then, on March 9, 2022, Defendant White told attendees at the Cowen 42nd Annual Health Care Conference that he and Verrica will “continue to work with the FDA toward an approval of YCANTH on or before ... May 24.” Jd. § 114. And on April 14, 2022, at the 21st Annual Needham Virtual Healtchare Conference, White stated that Verrica had hired a former FDA inspector to “go out and do mock inspections at all of our CMO facilities [including Sterling] to ensure that all our CMOs were inspection ready.” Jd. § 115. White also told attendees in response to an analyst’s question that he was “very optimistic” regarding the likelihood of FDA approval of the VP-102 NDA. /d. 4116. Finally, on May 9, 2022, in its SEC

Form 10-Q, Verrica stated that the FDA inspection of Sterling had met with a “satisfactory resolution.” /d. § 118. Yet, on May 24, 2022, Verrica informed the market that it had once again received a CRL for its VP-102 NDA, explaining that there were “deficiencies identified during a general reinspection of Sterling . . ., the contract manufacturing organization that manufactures Verrica’s bulk solution drug product.” /d. § 126. On May 25, 2022, Verrica’s share price fell 63.8%. Jd. 128. II. Legal Standard “The class action is an exception to the usual rule that litigation is conducted by and on behalf of the individual named parties only.” Wal-Mart Stores v. Dukes, 564 U.S. 338, 348 (2011) (citation modified). Class certification is “proper only if the trial court is satisfied, after a rigorous analysis, that the perquisites of Rule 23 are met.” Jn re Hydrogen Peroxide Antitrust Litig., 552 F.3d 305, 316 (3d Cir. 2008) (citing Gen. Tel. Co. of Sw. v. Falcon, 457 U.S. 147, 161 (1982)). The Court’s “rigorous analysis” focuses on “resolv[ing] all factual or legal disputes relevant to class certification, even if they overlap with the merits.” /d at 307. Here, it is Plaintiff's burden to “establish[] each element of Rule 23 by a preponderance of the evidence.” Marcus v. BMW of N. Am., LLC, 687 F.3d 583, 591 (3d Cir. 2012). Plaintiff must demonstrate, in accordance with Rule 23(a), that (1) the class is so numerous that joinder is impracticable; (2) there are questions of law or fact common to the class; (3) the claims or defenses of the representative parties are typical of the claims or defenses of the class; and (4) the representative parties will fairly and adequately protect the interests of the class. Fed. R. Civ. P. 23(a). Because Plaintiff seeks to certify a damages class under Rule 23(b)(3), Plaintiff must also demonstrate (5) that questions of law or fact common to class members predominate

over any questions affecting only individual members and (6) that a class action is superior to other available methods for fairly and efficiently adjudicating the controversy. Fed. R. Civ. P.

Free access — add to your briefcase to read the full text and ask questions with AI

Kranthi Gorlamari v. Verrica Pharmaceuticals, Inc. et al., (E.D. Pa. 2026).

Kranthi Gorlamari v. Verrica Pharmaceuticals, Inc. et al. (Kranthi Gorlamari v. Verrica Pharmaceuticals, Inc. et al.) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

Related

Affiliated Ute Citizens of Utah v. United States
406 U.S. 128 (Supreme Court, 1972)
General Telephone Co. of Southwest v. Falcon
457 U.S. 147 (Supreme Court, 1982)
Basic Inc. v. Levinson
485 U.S. 224 (Supreme Court, 1988)
In Re DVI, Inc. Securities Litigation
639 F.3d 623 (Third Circuit, 2011)
Erica P. John Fund, Inc. v. Halliburton Co.
131 S. Ct. 2179 (Supreme Court, 2011)
Wal-Mart Stores, Inc. v. Dukes
131 S. Ct. 2541 (Supreme Court, 2011)
Messner v. Northshore University HealthSystem
669 F.3d 802 (Seventh Circuit, 2012)
Baby Neal v. Casey
43 F.3d 48 (Third Circuit, 1994)
Marcus v. BMW of North America, LLC
687 F.3d 583 (Third Circuit, 2012)
In Re Hydrogen Peroxide Antitrust Litigation
552 F.3d 305 (Third Circuit, 2009)
Cammer v. Bloom
711 F. Supp. 1264 (D. New Jersey, 1989)
Crystal Byrd v. Aaron's Inc
784 F.3d 154 (Third Circuit, 2015)
Vince Mullins v. Direct Digital, LLC
795 F.3d 654 (Seventh Circuit, 2015)
Reynaldo Reyes v. Netdeposit
802 F.3d 469 (Third Circuit, 2015)
Tyson Foods, Inc. v. Bouaphakeo
577 U.S. 442 (Supreme Court, 2016)
Sam Hargrove v. Sleepys LLC
974 F.3d 467 (Third Circuit, 2020)
In re Schering Plough Corp. Erisa Litigation
589 F.3d 585 (Third Circuit, 2009)
Krogman v. Sterritt
202 F.R.D. 467 (N.D. Texas, 2001)