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... Abbott all of the filing materials and information in SuperGen's possession or control necessary for Abbott to develop the Product and file for Regulatory ... Leveraging the expertise of Abbott Laboratories in clinical research and regulatory compliance, this agreement lays the foundation for a successful ...Download Sales, Distribution and Development Agreement between Supergen, Inc. and Abbott Laboratories regarding clinical development, obtaining of regulatory ... This Sales, Distribution, and Development Agreement (the "Agreement") is made as of December 21, 1999 by and between SuperGen, Inc., ("SuperGen"), a California ... ... agreement with Abbott Laboratories for the co-exclusive distribution ... by increased clinical trials costs related to our efforts to obtain FDA approval of the. The costs of both GCP Audits shall be borne by AVI and SuperGen. If SuperGen is the Party responsible for the clinical development and regulatory approval of ... Mar 16, 2007 — Termination of Agreements with Abbott Laboratories. In December 1999, we entered into a Nipent distribution agreement with Abbott Laboratories. All companies that sell securities in the United States must register with the Securities and Exchange Commission (SEC) and file reports on a regular basis. ABBOTT LABORATORIES HEREBY DISCLAIMS ALL REPRESENTATIONS AND WARRANTIES, WHETHER EXPRESS OR IMPLIED, CREATED BY LAW, CONTRACT OR OTHERWISE, INCLUDING, WITHOUT ... ... in timelines for our potential products in development, including the obtaining of regulatory approvals;. •. delays in manufacturing or clinical trial plans;.