Balance the risks vs. rewards of Alnylam’s licensing strategy

Who is Dr. John Maraganore? Who are the stakeholders involved in the case and what are their roles? Why are they working (or not working) together collaboratively?

How do you balance the risks vs. rewards of Alnylam’s licensing strategy? What are its pros and cons? How should Alnylam sustain its IP and licensing strategy? Should Alnylam Pharmaceuticals convert its business model such that it becomes an intellectual property licensing company?

Are there specific aspects about RNA interference as a technology platform that make it easier or harder to develop and subsequently execute an intellectual property strategy to protect it?

Why are the co-owners of the Tuschl I patent arguing over the patent’s prosecution?

If Merck, through Sirna, has a license to Tuschl I, should it also need a license from Alnylam?

At what point, if ever, should Alnylam negotiate with Merck for a license to the latter’s intellectual property

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