Karyopharm Therapeutics Inc

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Case Summary
Company Name: Karyopharm Therapeutics Inc
Stock Symbol : NASDAQ: KPTI
Class Period Start: 03/02/2017
Class Period End: 02/22/2019
Lead Plaintiff motion: 09/23/2019
Date Filed: 07/23/2019
Type of Case: Securities Class Action
Court: U.S. District Court for the District of Massachusetts
Summary:

Thieler Law Corp advises investors with losses exceeding $100,000 of the September 23, 2019 lead plaintiff deadline in a class action lawsuit filed against Karyopharm Therapeutics Inc (NASDAQ: KPTI) (“Karyopharm” or “the Company”). The suit is pending in the U.S. District Court for the District of Massachusetts and investors, who purchased Karyopharm Therapeutics Inc securities between March 2, 2017 and February 22, 2019 and/or pursuant to the April 28, 2017 and May 7, 2018 common stock offerings, have until September 23, 2019 to move for lead plaintiff. You do not need to move for lead plaintiff to be a member of the Class.

If you purchased Karyopharm Therapeutics Inc securities during the Class Period, and have losses over $100,000, you may contact Thieler Law Corp by calling at (619) 377 - 4324 or emailing mail@thielerlaw.com . No class has been certified in this case, and if your losses are less than $100,000 you are still a member of the class.

The complaint alleges that during the Class Period defendants made false and misleading statements and/or allegedly failed to disclose that throughout the Class Period, the Company continued to tout the commercial prospects for selinexor and consistently described selinexor as having a “predictable and manageable tolerability profile” and a “very nice safety profile,” and assured investors that it was “well tolerated” by patients. Karyopharm also claimed that selinexor had the potential to be used as a new treatment for MM, with limited and manageable side effects. As a result of these misrepresentations, Karyopharm shares traded at artificially inflated prices during the Class Period.

On February 22, 2019 the FDA released a briefing document that expressed serious concerns with selinexor. According to the FDA, one of the previously cancelled selinexor trials had resulted in "worse overall survival" for certain patients treated with selinexor, which "highlight[ed] the toxicity of this drug."  The FDA concluded that "[t]reatment with selinexor is associated with significant toxicity" and has "limited efficacy."

Following this news, NASDAQ: KPTI fell from $8.97 per share on February 21, 2019 to $5.07 on February 22, 2019—a $3.90 or 43.48% drop.

If you were negatively impacted by your investment in Karyopharm Therapeutics Inc securities between March 2, 2017 and February 22, 2019 and/or pursuant to the April 28, 2017 and May 7, 2018 common stock offerings and would like to learn more about this lawsuit and your ability to participate as a lead plaintiff, please contact us for your no-cost evaluation.

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