NASDAQ:BMRN Investor Notice: Lawsuit Alleges Securities Laws Violations by BioMarin Pharmaceutical Inc.
A lawsuit was filed on behalf of investors in BioMarin Pharmaceutical Inc. (NASDAQ:BMRN) shares over alleged securities laws violations.
San Diego, CA -- (SBWire) -- 10/12/2020 --An investor, who purchased shares of BioMarin Pharmaceutical Inc. (NASDAQ: BMRN), filed a lawsuit over alleged Securities Laws violations by BioMarin Pharmaceutical Inc.
Investors who purchased shares of BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) have certain options and for certain investors are short and strict deadlines running. Deadline: November 24, 2020. NASDAQ: BMRN investors should contact the Shareholders Foundation at mail@shareholdersfoundation.com or call +1(858) 779 - 1554.
Based on BioMarin Pharmaceutical Inc's Phase 1/2 study results, the investing and medical community viewed valoctocogene roxaparvovec as a likely candidate for becoming the first gene therapy approved by the U.S. Food and Drug Administration ("FDA") for hemophilia in the U.S.
In May 2019, BioMarin Pharmaceutical Inc announced the interim results from its Phase 3 study of valoctocogene roxaparvovec for adults suffering from severe hemophilia A. The results, although showing the treatment's effectiveness, disappointed the market because they indicated a reduction in durability of effectiveness from the results shown in the Phase 1/2 results. That is, under the Phase 3 results, it was not clear whether valoctocogene roxaparvovec's effectiveness would last as long as indicated in the Phase 1/2 study, and thus, whether valoctocogene roxaparvovec would be a single treatment, or one requiring more than one treatment over the life of a patient. These concerns echoed those that first arose in 2018, after the Company reported a disappointing two-year update from the Phase 1/2 study, which showed factor VIII levels waning over time.
In December 2019, BioMarin Pharmaceutical Inc submitted a Biologics License Application ("BLA") to the FDA for valoctocogene roxaparvovec for adults with hemophilia A based on the interim analysis of the ongoing Phase 3 study of valoctocogene roxaparvovec, as well as three-year data from the Company's Phase 1/2 study of valoctocogene roxaparvovec. BioMarin also announced that the European Medicines Agency ("EMA") validated the Company's Marketing Authorization Application ("MAA") for valoctocogene roxaparvovec for adults with severe hemophilia A, with the MAA review to commence in January 2020 under accelerated assessment.
On August 19, 2020, BioMarin Pharmaceutical Inc announced receipt of a Complete Response Letter ("CRL") from FDA regarding the Company's BLA for valoctocogene roxaparvovec. Therein, the FDA concluded that the "differences between Study 270-201 (Phase 1/2) and the Phase 3 study limited its ability to rely on the Phase 1/2 study to support durability of effect." As a result, the FDA recommended that BioMarin "complete the Phase 3 Study and submit two-year follow-up safety and efficacy data on all study participants."
The plaintiff claims that between February 28, 2020 and August 18, 2020, the defendants made false and/or misleading statements and/or failed to disclose that differences between the Phase 1/2 and Phase 3 study of valoctocogene roxaparvovec limited the reliability of the Phase 1/2 study to support valoctocogene roxaparvovec's durability of effect, that as a result, it was foreseeable that the FDA would not approve the BLA for valoctocogene roxaparvovec without additional data, and that as a result, the Company's public statements were materially false and misleading at all relevant times.
Those who purchased shares of BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) have certain options and should contact the Shareholders Foundation.
Contact:
Shareholders Foundation, Inc.
Michael Daniels
3111 Camino Del Rio North - Suite 423
92108 San Diego
Phone: +1-(858)-779-1554
Fax: +1-(858)-605-5739
mail@shareholdersfoundation.com
About Shareholders Foundation, Inc.
The Shareholders Foundation, Inc. is a professional portfolio monitoring and settlement claim filing service, , which does research related to shareholder issues and informs investors of securities class actions, settlements, judgments, and other legal related news to the stock/financial market. Shareholders Foundation, Inc. is in contact with a large number of shareholders and offers help, support, and assistance for every shareholder. The Shareholders Foundation, Inc. is not a law firm. Referenced cases, investigation, and/or settlements are not filed/reached and/or related to Shareholders Foundation. The information is provided as a public service. It is not intended as legal advice and should not be relied upon.
Media Relations Contact
Michael Daniels
Shareholders Foundation
1-858-779-1554
https://shareholdersfoundation.com/
View this press release online at: http://rwire.com/1309144