According to the complaint, defendants made false and/or misleading statements and/or failed to disclose that:
- Jasper lacked the controls and procedures necessary to ensure that the third-party manufacturers on which it relied were manufacturing products in full accordance with cGMP regulations and otherwise suitable for use in clinical trials;
- the foregoing failure increased the risk that results of ongoing studies would be confounded, thereby negatively impacting the regulatory and commercial prospects of Jasper’s products, including briquilimab;
- the foregoing increased the likelihood of disruptive cost-reduction measures;
- accordingly, Jasper’s business and/or financial prospects, as well as briquilimab’s clinical and/or commercial prospects, were overstated; and
- as a result, defendants’ public statements were materially false and misleading at all relevant times.
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