Cardiometabolic · Weight management

Launch & scale global trials at market speed

As cardiometabolic pipelines expand, sponsors need to launch global studies in weeks, not months. Medable is built to help sponsors and CROs scale across indications, execute faster, and bring therapies to patients sooner.

Medable participant looking at computer screen

Move at market speed with data consistency that scales

  • 1–2 week go-live with reusable program assets
  • First study in 4–6 weeks with AI-assisted build, then 1–2 day UAT
  • Asset catalog reused portfolio-wide — dashboards, eCOA, translations
  • Real-time oversight with custom, on-demand exports
  • 95% participant adherence across global enterprise studies
  • eCOA, eConsent, and TeleVisit in one BYOD-compatible app
Platform reach

2K+

Global cardiometabolic sites on the Medable platform
Participation

24K+

Participants enrolled across cardiometabolic programs
Global

52

Distinct countries reached
Localization

86

Distinct locales supported

Cut initial study build timelines to two weeks or less with a program-led approach.

Animated interface of Medable AI generating eCOA screens from a user prompt about a sleep diary questionnaire.

Establish your standard

Make the operational investment once. Define reusable study components, translations, and integrations as your enterprise standard.

A horizontal gradient timeline with five evenly spaced checkmark icons connected by vertical lines, transitioning from dark purple on the left to light purple on the right.

Adapt and configure

Scale a single molecule across multiple indications with a reusable operational framework.

Accellerate delivery across program

From onboarding participants to data visualization, our platform delivers the flexibility and efficiency you need for today’s clinical research demands.

Built to match the momentum of cardiometabolic

35x

faster first-time eCOA build vs. manual, with AI-assisted configuration and localization

50%

reduction in initial study build time — roughly 80 hours saved per study

10–20 wks

reduction in country go-lives by running translations in parallel for simultaneous global launch

Operational AI for modern metabolic development

Medable’s AI helps your team process more data, faster, with human oversight and audit controls built in.

DDF Agent
Instantly transforms protocol documents into a structured, source-traceable digital study model that automates downstream study setup, documents, and clinical workflows.
AI-powered eCOA
eCOA configuration and accelerated localization for global deployment with participant and caregiver-friendly design to maintain high adherence.
Intelligent Consent
AI-powered eConsent and TeleVisit that streamline consent creation, review, and deployment in one participant app.
TMF Agent
Automates high-volume TMF filing every day to keep studies continuously inspection-ready with accurate, compliant documentation.
We have successfully completed the study with an impressive dosing compliance rate of 94.5%. To put this into perspective, our previous Sleep Apnea study had a compliance rate of 85–87%. This remarkable improvement is a testament to our strong partnership..."
TA Leader - Sleep Apnea Study
Top 5 Pharma

How a Top-10 Pharma standardized weight management trials and beat FPI by six weeks

Learn how a top-10 pharmaceutical company partnered with Medable to standardize a complex global weight management program spanning 70+ sites, accelerate study startup, improve the participant and site experience, and achieve First Patient In (FPI) six weeks ahead of schedule.

PDF
Case Study: Medable beats forecasted FPI date by taking eCOA off the critical path

Frequently asked questions

How fast can a cardiometabolic study go live?

With reusable program assets, initial build drops to 1–2 weeks and a 4-week path to operational readiness before FPI. AI-assisted build and parallel translation compress global go-live.

How do you keep long-duration weight-management patients engaged?

A BYOD-friendly app unifies eCOA, eConsent, and TeleVisit with smart reminders and branching logic, sustaining 95% participant adherence across global studies.

Can the platform scale across an expanding GLP-1 portfolio?

Yes. Reusable frameworks, an asset catalog, and consistent operational deployment let you design once and scale across cohorts, master protocols, and adaptive programs.

What does Operational AI handle?

Agentic AI assists eCOA configuration and localization, automates high-volume eTMF filing, and surfaces enrollment, compliance, and safety signals early, always human-in-the-loop.

See how Agent Studio can transform your trials.