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Alvotech (ALVO) Faces Investor Scrutiny Amid Manufacturing Deficiencies Severely Impacting Assurances of 2025 Revenues and Adjusted EBITDA, Stock Tumbles 33% -- Hagens Berman

Key Takeaway: Alvotech (ALVO) is under investigation by Hagens Berman due to concerns over its transparency regarding manufacturing operations and revenue forecasts. The scrutiny intensified after a major revision to its 2025 financial projections, prompted by a Complete Response Letter (CRL) from the FDA. This letter indicated deficiencies that must be resolved before the approval of its lead drug candidate, AVT05. As a result of the negative news, Alvotech's stock saw a significant drop of 33%, resulting in hundreds of millions lost in market value.

Market Sentiment Analysis

CONCERNS & RISKS

  • Alvotech faced significant scrutiny due to manufacturing deficiencies.
  • The company dramatically revised its financial forecasts downwards.
  • Shares tumbled 33% following the announcement of a Complete Response Letter (CRL) from the FDA.
  • Lowered adjusted EBITDA projections reflect serious operational issues.

Full Press Release Details

SAN FRANCISCO, Nov. 19, 2025 (GLOBE NEWSWIRE) -- Shareholder rights firm Hagens Berman is scrutinizing Icelandic biopharmaceutical company Alvotech (NASDAQ: ALVO) over the propriety of its disclosures regarding its lead drug candidate and its manufacturing operations, following a dramatic revision to the company’s full-year financial forecasts.
The firm urges investors in Alvotech who suffered significant losses to submit your losses now. The firm also encourages persons with knowledge who may be able to assist in the investigation to contact its attorneys.
Visit: www.hbsslaw.com/investor-fraud/alvo
Contact the Firm Now: ALVO@hbsslaw.com
844-916-0895
Alvotech (ALVO) Investigation:
The central focus of the inquiry revolves around whether Alvotech provided adequate transparency to the market concerning the status of its Biologics License Application (BLA) for AVT05—a critical biosimilar product—and the underlying manufacturing practices at its flagship Reykjavik facility. The assumptions related to these practices were "baked into" the company's ambitious 2025 revenue projections.
On May 8, 2025, Alvotech increased its full year revenue guidance for 2025 to $600-$700 million and full year adjusted EBITDA to $200-$280 million.
Three months later, on August 14, 2025, the company reiterated these robust forecasts. Furthermore, in its earnings commentary, management touted its pending marketing application for AVT05 in “major global markets,” asserting this momentum would make "the fourth quarter… by far the strongest one of this year.”
The narrative of steady growth was abruptly shattered on November 2, 2025, when Alvotech shocked investors when it announced the FDA issued a CRL that disclosed that “[t]e CRL noted that certain deficiencies, which were conveyed following the FDA’s pre-license inspection of Alvotech’s Reykjavik manufacturing facility that concluded in July 2025, must be satisfactorily resolved before this BLA for ATV05 can be approved.”
The company reduced its 2025 revenue to $570-$600 million and adjusted EBITDA to just $130-$150 million, respectively. These reductions were critical to investors because they amounted to lowered forecasted revenue range by about 10% below the prior midpoint and a whopping lowered adjusted EBITDA range by about 58% from the prior midpoint.
As to the latter, Alvotech stated it was “primarily driven by expected continuation of investments related to resolving certain facility issues, which also require a temporary slowdown in production.”
The news sent Alvotech shares crashing about 33% on November 3, 2025, wiping out hundreds of millions of dollars in market value in a single day.
“We’re focused on investors’ losses and whether Alvotech may have misled investors about its interactions with the FDA and the commercial prospects of ATV05,” said Reed Kathrein, the Hagens Berman partner leading the firm’s investigation.
If you invested in Alvotech and have substantial losses, or have knowledge that may assist the firm’s investigation, submit your losses now »
If you’d like more information and answers to frequently asked questions about the Alvotech investigation, read more »
Whistleblowers: Persons with non-public information regarding Alvotech should consider their options to help in the investigation or take advantage of the SEC Whistleblower program. Under the new program, whistleblowers who provide original information may receive rewards totaling up to 30 percent of any successful recovery made by the SEC. For more information, call Reed Kathrein at 844-916-0895 or email ALVO@hbsslaw.com.
Hagens Berman is a global plaintiffs’ rights complex litigation firm focusing on corporate accountability. The firm is home to a robust practice and represents investors as well as whistleblowers, workers, consumers and others in cases achieving real results for those harmed by corporate negligence and other wrongdoings. Hagens Berman’s team has secured more than $2.9 billion in this area of law. More about the firm and its successes can be found at hbsslaw.com. Follow the firm for updates and news at @ClassActionLaw.
Reed Kathrein, 844-916-0895

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Frequently Asked Questions

What is Hagens Berman investigating about Alvotech?

Hagens Berman is examining Alvotech's disclosures on its lead drug and manufacturing operations.

Why did Alvotech lower its 2025 revenue guidance?

Alvotech reduced its revenue guidance after the FDA issued a Complete Response Letter citing deficiencies.

What was the impact of Alvotech's announcement on stock prices?

Alvotech's announcement led to a 33% drop in its shares, erasing substantial market value.

How can investors report losses related to Alvotech?

Investors can submit their losses to Hagens Berman for assistance with the ongoing investigation.

Is there a program for whistleblowers related to Alvotech?

Yes, whistleblowers may receive rewards via the SEC Whistleblower program for original information.

Last updated: Nov 19, 2025