Huey v. Anavex Life Sciences Corporation

CourtCourt of Appeals for the Second Circuit
DecidedJune 26, 2026
Docket25-1752
StatusPublished

This text of Huey v. Anavex Life Sciences Corporation (Huey v. Anavex Life Sciences Corporation) is published on Counsel Stack Legal Research, covering Court of Appeals for the Second Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Huey v. Anavex Life Sciences Corporation, (2d Cir. 2026).

Opinion

25-1752 Huey v. Anavex Life Sciences Corporation

In the United States Court of Appeals For the Second Circuit

August Term, 2025 No. 25-1752

QUINTESSA HUEY, Plaintiff-Appellant,

JONATHAN BLUM, individually and on behalf of all others similarly situated, Plaintiff,

v.

ANAVEX LIFE SCIENCES CORPORATION, CHRISTOPHER U. MISSLING, Defendants-Appellees.

On Appeal from a Judgment of the United States District Court for the Southern District of New York.

ARGUED: FEBRUARY 12, 2026 DECIDED: JUNE 26, 2026

Before: JACOBS, CALABRESI, and NATHAN, Circuit Judges. Plaintiff-Appellant Quintessa Huey appeals from a judgment of the United States District Court for the Southern District of New York (McMahon, J.) dismissing her complaint and denying her request to replead. Huey held shares in Anavex Life Sciences Corporation (“Anavex”), a publicly traded biopharmaceutical company. Huey filed a putative class action against Anavex and its then-CEO, Christopher U. Missling, alleging securities fraud on the basis of an alleged misrepresentation. On the day that Defendants made a disclosure correcting the alleged misrepresentation, Anavex’s share price increased. The share price did not decline until the next two days, when it moved in tandem with the entire market. The district court held that Huey failed sufficiently to plead loss causation given the initial increase and delayed decline in Anavex’s share price. Because we agree that in light of these circumstances Huey failed plausibly to allege loss causation, we AFFIRM the judgment of the district court.

ADAM M. APTON, Levi & Korsinsky, LLP, New York, NY, for Plaintiff-Appellant.

STEPHEN G. TOPETZES (Theodore L. Kornobis, on the brief), K&L Gates LLP, Washington, DC, for Defendants-Appellees.

CALABRESI, Circuit Judge:

This case concerns what pleadings are necessary for a plaintiff sufficiently

to allege loss causation in a securities-fraud action under Section 10(b) of the

Securities Exchange Act.

2 Plaintiff-Appellant Quintessa Huey held shares in Anavex Life Sciences

Corporation (“Anavex”), a publicly traded biopharmaceutical company. Huey

filed a putative class action against Anavex and its then-CEO, Christopher U.

Missling, alleging that they misled investors by, among other things, implying in

various disclosures that the FDA had approved their methodology for measuring

a drug candidate’s efficacy in clinical trials. On the day Missling announced that

the company would abandon the purportedly FDA-approved methodology,

Anavex’s share price increased. The share price did not decline until the following

two days; at that time, it moved in tandem with the entire market.

The United States District Court for the Southern District of New York

(McMahon, J.) dismissed Huey’s complaint for failure to state a claim and denied

her request to replead. The district court held that Huey failed sufficiently to plead

loss causation given the initial increase then delayed decline in Anavex’s share

price, and the surrounding market context. Because we agree that Huey failed

plausibly to allege loss causation, we AFFIRM the judgment of the district court.

3 I. Background

A. Anavex Tests Proposed Treatment for Rett Syndrome

Anavex is a public biopharmaceutical company that specializes in early-

stage therapies for central nervous system diseases. In 2016, Anavex announced

that one of its drug candidates, ANAVEX 2-73, displayed “positive preclinical

data” for the treatment of Rett syndrome, a rare genetic neurological disease. P.A.

App’x at 16.

To obtain FDA approval to sell and market ANAVEX 2-73 for Rett

syndrome, Anavex conducted several clinical trials, including: a Phase 2 trial

beginning in June 2019 (the AVATAR trial) and a Phase 2/3 trial beginning in

September 2019 (the EXCELLENCE trial). As with all clinical trials, these studies

used standardized metrics known as “endpoints” to measure the efficacy of the

tested drug. One such endpoint is a patient’s improvement on the Rett Syndrome

Behavioral Questionnaire (“RSBQ”): a survey administered to a Rett syndrome

patient by her caregiver that assesses symptoms the patient is experiencing.

Another endpoint is a patient’s improvement on the Clinical Global Impression-

Improvement (CGI-I) scale: an assessment similar to RSBQ that is completed by a

patient’s clinician, rather than the patient herself. To improve accuracy, these two

4 metrics can be “anchored” to one another to ensure that a patient’s self-reported

improvements are tied to improvements also observed by a clinical professional.

Anavex was not the only company working on a Rett syndrome treatment.

A competitor pharmaceutical company, Neuren, developed a Rett syndrome drug

candidate called DAYBUE that had reached the end of its Phase 2 trials by 2017.

For DAYBUE’s final Phase 3 clinical trial, the FDA approved Neuren’s use of an

anchored RSBQ/CGI-I endpoint to measure the drug’s efficacy. Neuren used the

typical approach for measuring efficacy in clinical trials. This approach compared

the final, end-of-treatment RSBQ/CGI-I score with the baseline, pre-treatment

score to determine the patient’s net improvement (“RSBQ/CGI-I endpoint”). The

trial concluded in 2021 with positive results, and DAYBUE received marketing

approval from the FDA in March 2023.

Anavex took a different approach in its clinical trials of ANAVEX 2-73.

Rather than compare the baseline and end-of-treatment RSBQ/CGI-I scores for

each patient, Anavex decided to account also for scores reported during the trial

(i.e., mid-treatment RSBQ/CGI-I scores). Anavex called this approach RSBQ-AUC

(Area Under the Curve). By including mid-treatment scores in the measurement,

the RSBQ-AUC metric might reflect positive results although the end-of-treatment

5 score showed no improvement from the baseline. Indeed, the RSBQ-AUC result

could show a positive result even if the end-of-treatment score was lower than the

baseline (i.e., where a patient’s Rett syndrome symptoms were worse at the

conclusion of the study compared to when it began). Anavex thus could report

positive treatment effects for ANAVEX 2-73 using RSBQ-AUC although the

RSBQ/CGI-I endpoint used in the DAYBUE trial and approved by the FDA would

yield a neutral, or even a negative, effect.

B. Anavex’s Class Period Disclosures

During the Rett syndrome trials for ANAVEX 2-73, Defendants made

several public statements about the endpoints used and results obtained.

1. February 1, 2022, Statement

On February 1, 2022, Anavex hosted a special conference call to discuss the

AVATAR trial results. During the call, a research analyst asked Missling whether

the upcoming EXCELLENCE trial would use the same RSBQ-AUC endpoint as

the AVATAR trial. Missling replied, “So that’s right, the EXCELLENCE study will

use the same endpoint . . . because it’s just described, it is just the preference of the

FDA.” P.A. App’x at 37 (¶ 75) (emphasis added). He also said that the trial results

6 could potentially be used “to seek approval for Rett syndrome for adult patients.”

Id. at 40 (¶ 78).

2. February 2022 through January 2023 Statements

Over the course of the next year, Anavex and Missling made several

statements reiterating the company’s intention to use the same RSBQ-AUC

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