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BioVie (BIVI) Plunges After Alzheimer’s Drug Fails Phase 3 Due to “Protocol Deviations” at Trial Sites – Hagens Berman

Key Takeaway: BioVie Inc. (BIVI) is facing scrutiny following protocol deviations in its Phase 3 clinical trial for NE3107, an Alzheimer's drug. The company revealed significant non-compliance with Good Clinical Practice (GCP) at several trial sites, leading to the exclusion of patients from the study. As a result, BioVie's stock dropped sharply, prompting an investigation into the company's disclosures and potential misconduct. Hagens Berman is urging affected investors to come forward and report their losses due to these developments.

Market Sentiment Analysis

CONCERNS & RISKS

  • BioVie Inc. disclosed significant non-compliance with GCPs and regulations at trial sites.
  • The Phase 3 clinical trial of NE3107 missed statistical significance due to protocol deviations.
  • Hagens Berman is investigating whether BioVie concealed important information regarding GCP violations.
  • BioVie shares fell sharply in response to the trial's issues and subsequent announcements.

Full Press Release Details

SAN FRANCISCO, Jan. 11, 2024 (GLOBE NEWSWIRE) -- Hagens Berman urges BioVie Inc. (NASDAQ: BIVI) investors who suffered substantial losses to submit your losses now.
Contact An Attorney Now: BIVI@hbsslaw.com
BioVie Inc. (BIVI) Investigation:
The investigation focuses on the propriety of BioVie’s disclosures concerning its adherence to Good Clinical Practice (“GCP”) and protocols related to its Phase 3 clinical trial of NE3107, a potential Alzheimer’s disease drug.
On Sep. 26, 2023, BioVie announced completion of the last treatment visit in its Phase 3 clinical trial of NE3107.
But on Nov. 8, 2023, BioVie shocked investors when it revealed that “during routine monitoring of blinded data from our Phase 3 study of […] NE3107, we uncovered what appears to be potential scientific misconduct and significant non-compliance with GCPs and regulations at six sites[]” and “[w]e have alerted the FDA’s Office of Scientific Integrity (‘OSI’) about these issues[.]”
Then, on Nov. 29, 2023, BioVie announced that the Phase 3 trial missed statistical significance “due to site exclusions” and blamed the miss on “significant deviation from protocol and Good Clinical Practice (GCP) violations at 15 sites” leading it to exclude all patients from these sites and referrals of them to the OSI.
On an event call, BioVie’s management suggested that the company became aware of Phase 3 deviations beginning as early as July 2023.
In response to these disclosures, the price of BioVie shares fell sharply.
“We’re focused on investors’ losses and are investigating whether BioVie may have intentionally concealed GCP and protocol violations,” said Reed Kathrein, the Hagens Berman partner leading the investigation.
If you invested in BioVie 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 BioVie investigation, read more »
Whistleblowers: Persons with non-public information regarding BioVie 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 BIVI@hbsslaw.com.
Hagens Berman is a global plaintiffs’ rights complex litigation law firm focusing on corporate accountability through class-action law. The firm is home to a robust securities litigation practice and represents investors as well as whistleblowers, workers, consumers and others in cases achieving real results for those harmed by corporate negligence and fraud. More about the firm and its successes can be found at hbsslaw.com. Follow the firm for updates and news at @ClassActionLaw.
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Reed Kathrein, 844-916-0895

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Frequently Asked Questions

What is the focus of the BioVie investigation?

The investigation centers on BioVie’s compliance with Good Clinical Practice during its NE3107 trial.

What misconduct did BioVie reveal in November 2023?

BioVie disclosed potential scientific misconduct and GCP violations at six sites.

How did BioVie's trial results affect its stock price?

The stock price of BioVie dropped sharply following the disclosures about trial issues.

What should whistleblowers consider regarding BioVie?

Whistleblowers with relevant information may seek rewards through the SEC Whistleblower program.

Who can I contact for help regarding BioVie losses?

Investors can contact Hagens Berman at BIVI@hbsslaw.com for assistance.

Last updated: Jan 11, 2024