To: Miljenko Zuanic who wrote (3158) | 1/9/2018 2:47:15 PM | From: scaram(o)uche | | | >> At JPM, INCY was cautious on IDO1 <<
With all of the commentary about duration and deepening of the response, and with the slide showing data vs. historical for PD-1 alone? Emphasizing that nivo/epa results were as strong as pembro/epa? I got the opposite feel, that they were very strong re. IDO1. |
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To: former_pgs who wrote (3155) | 1/9/2018 3:29:40 PM | From: scaram(o)uche | | | These findings are important translationally, because they suggest broader clinical uses for D-1MT against cancers that overexpress any tryptophan catabolic enzyme (IDO1, IDO2 or TDO).
ncbi.nlm.nih.gov
>> does suggest one would make a mistake by extrapolating heavily based on the indoximod data <<
Yeah, but a mistake in which direction?? Isn't downstream inhibition of IDO1, IDO2 and TDO better than IDO1 alone??
The Incyte rationale for IOD1 selective agents is given here, third paragraph.....
ncbi.nlm.nih.gov
So they would say "no". |
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To: scaram(o)uche who wrote (3159) | 1/9/2018 3:42:07 PM | From: Miljenko Zuanic | | | Indeed, P2 Epa-PD1 chombo data v PD1 mono (multiple indications) are very strong, still Mr. Market expect much translating P2 data to P3. That was INCY position. If they do not believe in chombo they will never license MGA012 (let MRK and BMY promote "marginal" IDO1 data), or for any other in-house combination. They know that they can not depend on partners if they want full and fair benefit from their own drugs, Epa included. |
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To: tuck who wrote (3166) | 4/9/2018 10:55:00 AM | From: Miljenko Zuanic | | | Indeed, strong data for JAK1 Upadacitinib. Competition for GLPG/GILD too. Two Qs, are Humira response numbers bit on low side and why MACE/Death is pronounced in Humira/placebo? Bit biased in randomization, baseline unbalance?
OT: Nice move in QURE, too! |
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