Skip to main content

Make your next strategic decision with current evidence.

Maven brings live intelligence to biopharma research: answer strategic questions, identify changes that matter, and keep selected project files current with source-linked edits.

NICE · London · HTA assessment March 2025 draft

Lecanemab costs extend beyond the drug.

Infusion delivery and monitoring affect the cost model.

Matched to your forecast
Choose a document format
market_forecast.xlsx Updated
B4ƒxInclude infusion delivery + monitoring
Treatment cost assumptionsLecanemab
ABC
1Cost componentModel assumptionEvidence
2Drug acquisitionIncludedBaseline
3Infusion deliveryNot includedAdd administration costs NICE¹
4MonitoringNot includedAdd MRI + follow-up NICE¹
Cost assumptionsSources+

Upload or create files in a Maven project. Review sourced edits, roll back changes, and download the current version.

Company logos

Move from static research to live intelligence.

Periodic research

Files you have to refresh.

  1. Research

    Assemble the evidence for each analysis.

  2. Between reviews

    New developments leave the analysis behind.

  3. Next decision

    Find and assess what changed before you decide.

Live intelligence with Maven

Files Maven keeps current.

  1. Research

    Start with global evidence already connected.

  2. Between reviews

    Relevant changes reach your team and update selected working files.

  3. Next decision

    Review what changed and decide what comes next.

01

Cover more ground.

02

Spend less time catching up.

03

Make more room for judgment.

See what changes your next decision.

Trial amendment
HTA guidance
Company update

Your team’s priorities

Does DAPA-MI still test the outcome in our thesis?

Matched to your watchExample signal

DAPA-MI changes its primary endpoint.

Previous primary endpointCV death or heart-failure hospitalization
Revised primary endpoint7-component cardiometabolic composite

The original cardiovascular endpoint is now secondary. Reassess the thesis against both outcomes.

View evidence

The registry records a February 2023 amendment prompted by a lower-than-expected blinded event rate. The primary endpoint became a hierarchical cardiometabolic composite assessed using a win-ratio analysis. The original cardiovascular endpoint became secondary. The registry results were published on 7 July 2024.

EU trial register · Amendment 23 Feb 2023

Expand your view beyond the sources you can follow by hand.

Connect company updates, clinical evidence, regulatory decisions, and local market access to the assets and markets you follow.

Explore Live Intelligence
Sources across the world
Source locations Highlighted: Companies
Signal detection

Use Maven’s intelligence wherever your team works.

Live intelligence for teams across biopharma.

See what your team can do with live intelligence.