AI Assist
Freemium
Users prioritizing on-device processing and data privacy
A senior scientist spending three months on a systematic literature review is three months not running experiments — and most teams accept that cost because they don't have an alternative that doesn't just return a pile of PDFs.
Lumaris generates structured intelligence reports from a defined therapeutic question, pulling across PubMed, bioRxiv, clinical trial registries, patent literature, and preprint servers — the vendor states 35M+ papers indexed, updated daily. You define the scope, an onboarding team helps frame the question, and a cited report with evidence strength ratings and identified gaps arrives within 48 hours. That workflow fits well for a pre-IND competitive scan or a target validation brief ahead of a portfolio review. It breaks down when your team needs continuous monitoring with alerts rather than discrete on-demand reports, or when the question requires proprietary internal data woven into the synthesis. There is no API, so nothing this tool produces feeds automatically into your existing R&D data stack.
Bottom line: Bet on Lumaris when you need a defensible literature synthesis fast before a board meeting or partnering discussion — not when you need a live feed of signals piped into your own pipeline.
Single $49 brief
$499 one-time
$1,499 per quarter
View full pricing on lumaris.nanocorp.app →
Pricing may have changed since last verified. Check the official site for current plans.
Find your fit
More options in Productivity. Compare pricing, platforms, and features side by side.
Freemium
Users prioritizing on-device processing and data privacy
Free
Users seeking culturally grounded AI responses
A senior scientist spending three months on a systematic literature review is three months not running experiments — and most teams accept that cost because they don’t have an alternative that doesn’t just return a pile of PDFs.
Lumaris generates structured intelligence reports from a defined therapeutic question. It pulls across PubMed, bioRxiv, clinical trial registries, patent literature, and preprint servers. The vendor states 35M+ papers indexed, updated daily. Users define the scope, an onboarding team helps frame the question, and a cited report with evidence strength ratings and identified gaps arrives within 48 hours. The workflow fits well for a pre-IND competitive scan or a target validation brief ahead of a portfolio review. It breaks down when teams need continuous monitoring with alerts rather than one-off reports.
Pros include synthesizing findings across sources into a single cited report, covering negative results and failed trials, and scoping help from an onboarding team. Free sample report available on request. Cons are the lack of an API or integration path, plus the on-demand model rather than live alerts. Use cases cover drug target identification, competitive landscape mapping, safety signal detection, post-trial literature synthesis, and pipeline whitespace analysis.
Best for pharma R&D teams in oncology, CNS and metabolic disease programs, competitive intelligence analysts, and target validation scientists. Teams needing real-time monitoring of a therapeutic area or automatic flow into internal pipelines should skip it and look at dedicated competitive intelligence platforms instead.
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