Valneva SE/€VLA

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About Valneva SE

Valneva SE is a biotechnology company specializing in the development and commercialization of vaccines for infectious diseases. The company's portfolio includes vaccines for diseases such as Japanese encephalitis and cholera. Valneva is actively engaged in developing vaccines for Lyme disease and chikungunya. Founded in 2013 through the merger of Intercell AG and Vivalis, Valneva is headquartered in Saint-Herblain, France. The company operates primarily in Europe but has a global reach through various strategic partnerships and licensing agreements. Valneva's competitive strength lies in its focus on addressing unmet medical needs with its diverse pipeline of innovative vaccine candidates.

Ticker

€VLA
Sector

Primary listing

PAR

Employees

700

Valneva SE Metrics

BasicAdvanced
€698M
-
-€0.42
1.01
-

Bulls say / Bears say

The EMA lifted its temporary restriction on Ixchiq for adults aged 65 and over after a comprehensive safety review, enabling resumed use in elderly populations at significant risk of chikungunya (Reuters)
Ixchiq generated €7.5 million in the first half of 2025, representing over 8% of Valneva’s total product sales, and brokerage Kempen noted the share sell-off as an attractive buying opportunity (Reuters)
In June 2025, Valneva secured a three-year exclusive marketing and distribution agreement with CSL Seqirus for Germany, covering its chikungunya, Japanese encephalitis, and cholera vaccines with minimum annual purchase commitments to bolster European market penetration (Nasdaq)
The U.S. FDA suspended the license for Valneva’s chikungunya vaccine Ixchiq following four serious adverse event reports, forcing an immediate halt to U.S. distribution and sales (Reuters)
Valneva’s shares plunged about 25% on August 25, 2025 after the FDA suspension announcement, underscoring market concerns over a potential permanent withdrawal from the U.S. market (Reuters)
The EMA’s revised product information restricts Ixchiq use in immunocompromised patients and requires thorough benefit-risk assessment, narrowing the eligible patient population and limiting market size (Reuters)
Data summarised monthly by Lightyear AI. Last updated on 5 Oct 2025.
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Market data provided by CBOE Europe and Deutsche Börse.

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