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ghmm

10/06/10 4:13 PM

#105710 RE: jq1234 #105707

Interesting, can't say that would have been my first guess at what they would do. No (direct) mention of the follow-on so I take it by ending the collaboration all other compounds return to InterMune.

I guess this won't change Dew's opinion of the compound's future :-).
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DewDiligence

10/06/10 4:17 PM

#105711 RE: jq1234 #105707

ITMN—I interpret the news as Roche’s agreeing to pay $175M merely to be free and clear of contractual obligations stemming from the 2006 Roche-ITMN partnership for HCV protease inhibitors. Inasmuch as there are newer and better PI’s available, I doubt that Roche will advance ITMN-191 to phase-3.

That ITMN-191 does not have what it takes is old news: e.g. #msg-46797334, #msg-53621981, #msg-53624063.
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turtlepower

10/06/10 6:15 PM

#105725 RE: jq1234 #105707

I wonder if ARRY gets a cut of that 175 M
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DewDiligence

04/15/13 4:22 PM

#159901 RE: jq1234 #105707

Is Danoprevir (f/k/a ITMN-191) good enough for China? Roche's partner thinks so:

http://www.reuters.com/article/2013/04/15/roche-idUSL5N0D209220130415

Roche Holding AG said it had teamed up with emerging biotech firm Ascletis to develop and commercialise its investigational drug danoprevir in China for the treatment of the hepatitis C virus.

Under the agreement, Ascletis will fund, develop and manufacture danoprevir in greater China, including Taiwan, Hong Kong and Macau and will also be responsible for regulatory affairs.

Danoprevir is a first-generation PI that must be given with interferon and ribavirin and is active in genotype-1/4. Roche paid ITMN $175M for the worldwide rights to Danprevir in Oct 2010 (#msg-55244199); maybe Roche will eventually get a return on the investment.