A 71-patient study reported a 12-week lung-function signal: mean forced vital capacity rose 98.4 ml in the highest-dose group and fell 20.3 ml with placebo.
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This provides controlled human evidence for Insilico’s drug-development case, but the small, short study does not establish pivotal efficacy.
Recursion reports an early patient signal for REC-4881
In its second-quarter results release, Schrödinger reported $32.5 million of software revenue at a 71% gross margin, alongside $23 million of drug-discovery revenue that included a $10 million milestone.
Insilico announces first dosing in rentosertib phase III
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Rentosertib’s randomized phase IIa results are published
[3]A 71-patient study reported a 12-week lung-function signal: mean forced vital capacity rose 98.4 ml in the highest-dose group and fell 20.3 ml with placebo.
This provides controlled human evidence for Insilico’s drug-development case, but the small, short study does not establish pivotal efficacy.
Recursion reports an early patient signal for REC-4881
[21]Recursion reported a median 43% reduction in polyp burden among 12 efficacy-evaluable patients in its open-label TUPELO study.
Schrödinger announces TuneLab access through LiveDesign
[6]Schrödinger said its LiveDesign platform would be a priority interface for participating biotech companies to access Lilly’s TuneLab workflows.
Lilly and NVIDIA announce an AI drug-discovery lab
[12]The companies announced up to $1 billion of joint investment in talent, infrastructure and compute over five years.
Roche announces its NVIDIA AI factory
[10]Roche described 2,176 on-premises GPUs and combined on-premises and cloud infrastructure exceeding 3,500 Blackwell GPUs.
Schrödinger reports its software and discovery revenue mix
[5]In its second-quarter results release, Schrödinger reported $32.5 million of software revenue at a 71% gross margin, alongside $23 million of drug-discovery revenue that included a $10 million milestone.
Insilico announces first dosing in rentosertib phase III
[4]Insilico announced first patient dosing in its Chinese GENESIS-IPF-3 study. The planned trial has 320 participants and 52 weeks of treatment.
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