Public-data intelligence for pharma strategy

Know where to look next.

Treelip turns complex public clinical, patent, regulatory, and biomarker records into explainable signals for research, diligence, and strategic planning.

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public trial records analyzed
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oncology ADC targets mapped
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LOE candidates screened
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focused intelligence modules
✓ FDA Orange Book✓ ClinicalTrials.gov✓ Transparent methodology
Clinical SurveillanceLive

Clinical Program Risk Radar

Focus diligence on oncology Phase 2 assets with public signals for delays, terminations, recruitment burden, and missing results.

9MW2821
Solid Tumors · Mabwell (Shanghai) Bioscience Co., .
Timeline Staleness
aldesleukin
Melanoma (Skin) · Saint Francis Hospital
Registry Stop
Belantamab mafodotin
AL Amyloidosis · Stichting European Myeloma Network
Registry Stop
ClinicalTrials.govRegistry snapshots
Patent IntelligenceLive

Generic Entry Radar

Screen U.S. small-molecule products for potential loss-of-exclusivity windows, with public expiry and patent-complexity signals in one view.

FDA Orange BookClinicalTrials.gov
Clinical + PatentLive

ADC Target Strategy Radar

Compare oncology ADC targets through clinical crowding, sponsor activity, patent-density signals, and strategic labels.

ClinicalTrials.govPatent signals
Translational BDLive

Translational Deal Radar

Identify translational programs that merit deeper diligence using public clinical momentum, IP-linkage, and BD-relevance signals.

ClinicalTrials.govPatent signals
Trial DesignLive

Protocol Benchmark Radar

Compare public trial designs by endpoint precedent, eligibility burden, biomarker strategy, and operational considerations.

ClinicalTrials.govRegistry text
Precision OncologyLive

Biomarker Patient-Selection Radar

See how oncology biomarkers are used for patient selection alongside FDA companion-diagnostic context and diagnostic patent-density signals.

ClinicalTrials.govFDA CDx data

Built for a specific question

Public biomedical databases contain valuable evidence, but raw search results are difficult to compare. Each Treelip module organizes the relevant records around a practical research or strategy question.

Evidence stays visible

Signals are clearly labelled and tied to public source records and methodology. Treelip is designed to support expert review, not to hide judgment behind a black-box score.

Start broad, investigate deeply

Use the dashboards to identify where attention may be warranted, then bring the underlying records, your team's expertise, and deeper diligence to the decision.

Pharma / BiotechBusiness DevFinance & InvestorsCROsDiagnosticsGeneric PharmaMarket Intelligence
About Treelip

A practical starting point for pharma strategy

Treelip is an independent platform for pharma, biotech, diagnostics, and investment teams. Its focused intelligence modules organize publicly available data from sources including FDA resources, ClinicalTrials.gov, and related public records into useful first-pass views for BD, strategy, and market intelligence work.

The outputs are designed for first-pass prioritization and expert review support, not automated decisions. Treelip does not replace clinical, legal, regulatory, or investment judgment; it helps experts decide what to investigate next.

Ways to work with Treelip: Public dashboards · Gated CSV exports · Custom asset or target reports · Watchlist monitoring.

Get Access

Bring a sharper starting point to your next review

Register your interest to request access, receive relevant product updates, or discuss a focused asset, target, or therapeutic-area question.

We store your name, work email, tool selections, CSV delivery preferences, notes, timestamp, source page, and any optional company or request details for internal follow-up. Submissions may be saved in access-controlled internal records and forwarded to Treelip team inboxes for manual response. Review our Privacy Policy and Accessibility Statement. Do not submit confidential or commercially sensitive information through this form.