Revonode
The platform

The whole deal management in a single interface

Data room management alongside the AI due diligence report, and surface the evidence behind any claim without leaving the page.

Data room

Conditional

Source confidence

62

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Revonode report

Diligence chat

Does the Phase 2 data support the efficacy claim in the deck?

Revonode

Partly. The deck claims a 68% responder rate; the study report gives 68% for the 100 µg arm only, n=23, with no active comparator. The pooled figure across all arms is 54%. Two of the three cited supporting papers sit behind programmes that failed in humans — down-weighted, not hidden.

ViewerCompany_pitch_deck.pdf

Due diligence report

Ilvaren Bio

01 · Executive summary

Ilvaren Bio presents a late-stage RNAi asset with credible oncology positioning. Efficacy evidence is real but narrower than presented, and the CMC record has one material gap. Recommendation is conditional on resolving the comparator question.

02 · Evidence ledger

ClaimSourceGrade
Orphan designation filedDeck slide 11Gap

Illustrative dataset — the interface is live, the deal is invented.

The confidence

Every answer carries its receipt

An answer you cannot check is not diligence. Every claim the platform makes is traced to the page it came from, not to a plausible-sounding summary. Open the receipt and you land on the source.

Compare

All seven dimensions, side by side

Science, clinical and safety, IP, manufacturing, regulatory, market and team — every asset scored across the same seven, from bound signals rather than sentiment. No dimension skipped because a specialist wasn't free, and no asset judged on a different basis from the one beside it.

Four assets scored across seven diligence dimensions
DimensionIlvaren Bio62Conditional · 3 openCardra Therapeutics60Conditional · 5 openKessendra Bio58Conditional · 2 openThexoria Therapeutics35No-go · 9 open
Science
Clinical & safety
IP / FTO
CMC
Regulatory
Market
Team
Binding riskNo FTO opinion; delivery chemistry overlaps a third-party family.No human efficacy data past Phase 1 — platform, not asset.Crowded indication; two competitors ahead on the same target.9 unresolved questions; evidence base sits behind discontinued programmes.

Each cell is clickable — it opens the signals behind that dimension. Illustrative dataset — the interface is live, the deal is invented.

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