![]() |
Advanced Search |
|
Compound PartneringCompound partnering demonstrates our ability to reduce development timelines by applying proven solutions leveraged from our extensive global experience. We believe our success in compound partnering evolves from our effective contingency planning. Using our vast development experience, we are able to predict many potential outcomes and then address those potential scenarios in contingency plans that provide flexibility and the ability to adapt quickly, if necessary. We bridge steps in drug development by conducting earlier elements of a study while simultaneously planning for later phases of work. This strategic planning and use of best practices effectively speeds the process, enabling us to shorten timelines, assess risks and make key decisions more quickly. One example of the successful application of this approach is our collaboration with Syrrx, Inc./Takeda Pharmaceutical Company Limited on the development of dipeptidyl peptidase IV (DPP-4) inhibitors for the treatment of type 2 diabetes. In this alliance, PPD and its partner took a compound from lead optimization to filing of a new drug application with the U.S. Food and Drug Administration in just 49 months. Partnering Criteria We look for compounds at pre-IND to Phase I with a straightforward, reasonably short development profile and clear regulatory path. Why Partner With PPD? In addition to extensive experience with alliances and a track record of successful development programs, other reasons to partner with PPD include:
PPD Pipeline We are currently advancing four partnered compounds at various stages of development and are actively seeking additional compounds to in-license/partner.
|
|
|||||||||
|
|||||