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Recent Research


JNJ: Novel next generation assets
We present an update to our September 2020 detailed pipeline analysis “J&J NME pipeline”, examining the prospects of three new molecular ent
Mar 7, 2022


Factor XIa: another anticoagulant? Not Quite. Could be gold standard
While uncharted territory inhibiting poorly investigated factor XIa, novel mechanism of action and early data and epidemiological studies suggest it could become the gold standard in Stroke prevention.
Jul 10, 2021


Keytruda Chemo combo approved despite more deaths and no survival benefit
Last night the FDA granted accelerated approval for Merck’s Keytruda to be used in combination with pemetrexed and carboplatin chemo for...
May 10, 2017


ROG:XV: PDL1 Tecentriq predictably worse on overall survival than PD1s again
Predictable failure of ROG anti PDL1 Tecentriq in Bladder cancer where anti PD1 succeeded: As we feared, Roche today announced that its...
May 9, 2017


Anti PD-L1s continue lacklustre rivalry with anti PD-1s
AstraZeneca received accelerated FDA approval for its anti PD-L1 durvalumab (Imfinzi) in 2nd line bladder cancer last week, making this...
May 8, 2017


High Hurdle for IDOs
IDOs from Incyte are back in focus with high response rates and better safety than the existing IO combos. But will they win out...
Apr 15, 2017


ROG.VX: FDA Label-Ocrevus ineffective in women with breast cancer risk
Despite ROG last week’s Ocrevus FDA approval for PPMS & RRMS, its lack of benefit in women with PPMS and increased cancer risk and little di
Apr 3, 2017


ROG:VX: APHINITY headline positive but await full data
Awaiting full data: Roche announced that APHINITY met its primary endpoint , but as expected details are to be published at an upcoming...
Mar 2, 2017


ROG.VX: APHINITY too close for comfort
We present the third update of our APHINITY analysis, originally published two years ago and find the risks of early stage Perjeta...
Feb 6, 2017


BMY.US: No Accelerated pathway does not imply registrational failure
Bristol's announcement that it is not pursuing an accelerated FDA approval pathway for Yervoy and Opdivo in first line lung cancer was...
Jan 20, 2017
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