Intercept Pharmaceuticals Inc. (NASDAQ: ICPT) shares are up 30% after announcing an agreement to sell some of its foreign subsidiaries plus rights to its international operation, including the Ocaliva commercialization license outside the US, to Advanz Pharma. Advanz is a pharmaceutical firm with a strategic focus on hospital and specialty pharmaceuticals in the EU.
Intercept to receive $405 million in upfront payment on closing
CEO and President of Intercept Jerry Durso said:
This agreement marks an important step forward for Intercept as the value it brings to our company allows us to significantly strengthen our balance sheet while providing us with greater strategic optionality during this transformational year and beyond.
After closing, Advanz Pharma will pay Intercept Pharmaceuticals an upfront payment of $405 million. Advanz Pharma will contribute another $45 million if the Intercept receives a pediatric orphan exclusivity extension in Europe. If Advanz Pharma seeks marketing authorization for obeticholic acid in NASH beyond the United States, Intercept could receive compensation on future net revenue of the drug.
Intercept to keep manufacturing and distributing obeticholic acid globally
Intercept shall retain the manufacture and distribution of obeticholic acid worldwide, while Advanz Pharma will be in charge of packing, distribution, and marketing throughout all markets beyond the United States.
Outside of the United States, a large percentage of Intercept employees will join Advanz Pharma. Intercept will keep hiring the remaining global staff. Also, Intercept will keep a presence in the United Kingdom to oversee its worldwide supply chain, assist its quality team, and conduct worldwide clinical trials. Durso added:
We are committed to investing in our core focus areas in the US, including our PBC business, potential future activities in NASH, and our advancing and expanding pipeline. At the same time, we are confident that the strong international team will continue to build on our successful PBC business as they transition to Advanz Pharma.
Ocaliva was given temporary authorization by the European Commission in December 2016 for PBC treatment in adults with an adverse reaction to UDCA or as a single agent in adults who can’t tolerate UDCA. It is now approved in over 40 countries around the world.
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