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SHIELD CLIENT / DEMO ENVIRONMENT SAMPLE SIGNALS ONLY NO LIVE API CONNECTIONS
AimwellBio Intelligence Platform
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Intelligence Dashboard
Shield Tier — Last refreshed: Apr 19, 2026 — 09:14 UTC
Threat Alert: 1 Active (Sample preview)
Sample data. Alert configuration is in activation and set up during onboarding. EMA safety signal detected for semaglutide class — thyroid C-cell tumor association under review. 2 of your 12 protected assets may be affected. View details
SENTINEL · THREAT SURFACE (SAMPLE PREVIEW)
12 sample severities · 1 critical · 3 high · 5 medium · 3 low
ADVERSARIAL VALIDATION · LAST 5 VERDICTS
Active Signals
89
across 6 data sources
Dossiers
7/10
3 remaining this month
Protected Assets
12
2 flagged for review
Threat Alerts
1
1 active, 0 critical
Pending Setup
  • Competitor monitoring configuration Our team will contact you to configure your watchlist.
  • Slack workspace integration Slack invite is initiated during onboarding, subject to eligibility.
  • Priority support Priority support workflow in activation. Response routing subject to onboarding and availability. Contact: support@aimwellbio.com
Cortex AI — Biopharma Intelligence Engine
Shield: 150 queries/mo
MV
You
What are the FDA fast-track pathways for GLP-1 drugs?
CX
Cortex
FDA offers three primary expedited pathways relevant to GLP-1 receptor agonists: Fast Track Designation (FTD), which can be requested at any development stage and enables rolling review; Breakthrough Therapy Designation (BTD), reserved for drugs showing substantial improvement over existing therapy on a clinically significant endpoint — semaglutide's cardiovascular indications leveraged this pathway; and Accelerated Approval, permissible when a surrogate or intermediate endpoint is reasonably likely to predict clinical benefit. For a GLP-1 asset in metabolic disease, FTD is typically fastest (FDA responds within 60 days), while BTD carries the most significant trial design and review benefits. Cortex has also flagged a new draft FDA guidance on GLP-1 label expansion from March 2026 — added to your protected asset watch list.
MV
You
Which competitors have Phase 3 data?
CX
Cortex
Key GLP-1 assets with Phase 3 data (Q1 2026): Novo Nordisk's semaglutide (SELECT CV outcomes, STEP obesity), Eli Lilly's tirzepatide (SURMOUNT-4 extension, SURPASS-CVOT 78-week data), Amgen's maridebart cafraglutide (OASIS-1 enrollment complete). Your Shield tier includes competitor dossiers — a sample for these assets is shown below in Competitor Dossiers. Live dossiers generate once your watchlist is connected during onboarding. Roche/Zealand's petrelintide remains Phase 2b.
Try:
Signal Feed
Sample preview
ClinicalTrials Clinical
Amgen MariTide OASIS-1 Completes 1,840-Patient Enrollment Ahead of Q2 2026 Target
Apr 17, 2026 Confidence: 95% HIGH
Reuters Competitive
AstraZeneca in Talks to License Hanmi's GLP-1/GIP Triple Agonist — Deal Valued at $2.4B
Apr 16, 2026 Confidence: 87% MEDIUM
FDA Regulatory
Draft Guidance Issued: Patient-Reported Outcome Measures in Obesity NDA Submissions
Apr 14, 2026 Confidence: 99% LOW
Protected Assets — Intelligence Watch List
12 Assets
Semaglutide CV labeling
Tirzepatide obesity NDA
MariTide Phase 3 data
SURMOUNT-4 extension
GLP-1 thyroid safety review
EMA semaglutide PRAC
Petrelintide Phase 2b
Hanmi GLP-1 licensing
FDA obesity guidance draft
CVOT regulatory framework
Oral GLP-1 bioavailability
GLP-1 renal outcomes data
Public Profile Preview — what others see
View Public Profile ↓
Competitor Dossiers
Sample preview · In activation
SAMPLE — generated from fixture data. Connect your watchlist to produce live dossiers.

Competitor Intelligence Dossier — 3 assets

Watchlist: semaglutide, tirzepatide, maridebart cafraglutide · Generated 2026-05-30T00:00:00Z · Overall confidence 54%

semaglutide 93% confidence · 2 sources

  1. [S1] Clinical data — SELECT CV outcomes 5y follow-up (2026-01-15) source conf 90%
  2. [S2] Regulatory filing — FDA label expansion draft guidance (2026-03-02) source conf 95%

tirzepatide 70% confidence · 2 sources

  1. [S1] Clinical data — SURPASS-CVOT 78-week data (2026-02-10) source conf 90%
  2. [S2] Company press release — Lilly Q4 pipeline update (2026-02-28) conf 50%

maridebart cafraglutide 0% confidence · 0 sources

  1. No sources on file for this asset yet.
SHIELD → COMMAND

How would your team move if every threat came with a verdict?

Shield surfaces what to watch. Command answers what to do next. Each signal in your queue arrives with adversarial validation already complete — PROCEED, DELAY, or KILL — sourced to its primary evidence and confidence-scored before it reaches your inbox.

Unlimited Cortex queries SCOUT automated runs Adversarial validation on every signal Unlimited dossiers Source-traced decision integrity
Upgrade to Command →
Confidence-scored · Source-traced · Adversarially validated
What you have on Shield
Your plan
Active now
AIMN:VERDICT generation — source-traced answers on demand.
Vault read & write — your team’s saved intelligence.
Atlas access — the indexed source graph.
In activation
Signal feed, alerts, watchlist, dossier, and competitor monitoring are included in Shield and are being switched on during onboarding. Anything labeled Sample on this page is illustrative until your data is activated.
Your next best step
Get value today
Your verdict engine and vault are active right now. While alerts and monitoring finish activating, the fastest way to put Shield to work today is to run a real decision through AIMN:VERDICT and save the verdict to your team vault.
Run a verdict Set up your watchlist for activation
If you move up to Command
Upgrade path
Shield is built for a team that needs to see the field clearly. Command is built for an organization where decisions need to be defensible.
  • A higher included AIMN:VERDICT allowance for heavier query volume.
  • Adversarial validation and source-traced decision integrity on the work that matters most.
  • A dedicated onboarding path — Command is set up with our team, not self-serve.
Talk to us about Command
The Dossier layer
Source-chain
Underneath every verdict sits a source-chain: each item traced to its primary record — PubMed, the FDA, ClinicalTrials.gov, SEC EDGAR — with the date it was published and the date we compiled it. The dossier engine that assembles this chain runs server-side and is gated to your Shield entitlement. We have published one real compiled sample so you can read the layer before your own watchlist is switched on.
  • Every line in the sample is drawn from the compiled signal corpus — no invented citations.
  • Each item carries source, source method, category, severity, sponsor, and provenance URL.
  • Automated, watchlist-driven generation against your own entities is in activation — included in Shield, being switched on during onboarding.
Read the sample dossier → Set up your watchlist for activation
Sample dossier · decision-support only · automated generation in activation (Shield entitlement). Simulation of dossiers against hypothetical scenarios is also in activation.
Run the dossier engine at scale on Command
Sales-assisted
When your team needs dossiers across many entities with adversarial validation and source-traced decision integrity on each one, Command is the tier built for it. Command is set up with our team, not self-serve — so the engine is tuned to your watchlist before it produces a single brief.
Talk to us about Command
What your Shield membership keeps doing for you
Your value
While your membership is active, your verdict engine, your team vault, and Atlas access stay on, and the work your team saves stays yours to return to. Alerts, watchlist, dossier, and competitor monitoring keep moving toward activation. You can review or change your plan any time from billing.
Manage billing & subscription →

Your Shield membership — status & next step

Where your plan standsShield · active
Verdict engine, team vault & Atlas accessActive now
Scheduled dossier preparationIn activation
Competitor & watchlist monitoringIn activation
Confirm dossier scope with your teamRequires onboarding
What's in the corpus behind your dossiersCurated · scheduled
9,270
signals
383
companies
9
areas
4
source types

Dataset-level totals across the curated corpus — PubMed/NCBI, U.S. FDA, ClinicalTrials.gov, and SEC EDGAR. Counts reflect the most recent scheduled compile — a curated snapshot, not a streaming source.

Your next best move

Review a dossier sample, then request your dossier setup so we can scope the indication areas and competitors your team needs covered. That is what turns Shield from "active" into a working paper trail.

Next tier — Command: adds organization-wide configuration and a dedicated point of contact, built for teams running multiple programs. Command is sales-assisted — talk to us to scope it.

If you cancel

Your verdict engine, team vault, and Atlas access switch off, and dossier and competitor monitoring stop moving toward activation. Everything your team has already saved stays exportable while your plan is active — pull anything you need to keep before the period ends.

Refer a colleague

Share a dossier sample with a colleague who owns a competing or adjacent program — it is the clearest demonstration of what Shield produces.

AimwellBio provides decision-support intelligence. It is not medical, legal, regulatory, or investment advice. Sources and outputs should be reviewed by qualified professionals before action.