NEWS: Curebase closes $40M Series B with strategic investment by Gilead. Read about it in TechCrunch, Fierce Biotech, andEndpoints News.

17K
Patients
enrolled
97%
Patient
Satisfaction1
89%
retention2
1. From IBS PDT study. 2. In smoking cessation DTx study
All-in-one solution

Modern, flexible long-term follow-up research.

Expand geographic access with Curebase’s virtual sites powered by purpose-built software for better retention and easier monitoring on studies running for months to years.

17K
Patients
enrolled
97%
Patient
Satisfaction1
89%
retention2
1. From IBS PDT study. 2. In smoking cessation DTx study
All-in-one solution

Modern, flexible long-term follow-up research.

Curebase has the most experience running end-to-end, regulatory-grade digital therapeutics (DTx) studies with purpose-built technology for faster recruitment, better retention, and greater diversity.

17K
Patients
enrolled
97%
Patient
Satisfaction1
89%
retention2
1. From IBS PDT study. 2. In smoking cessation DTx study
All-in-one solution

Modern, flexible long-term follow-up research.

Curebase is the only partner you need to run your study from start to finish with purpose-built technology for faster recruitment, greater diversity, and better patient experience.

The most comprehensive, tech-driven solution for real-world long term follow-up research.

Leverage our virtual site models powered by best-in-class patient engagement tools, real-time analytics, and in-house management services.

Trial Management Services

  • Trial management
  • Data management
  • Submissions
  • Remote monitoring
  • Recruitment

Virtual & Hybrid Sites

  • Virtual Clinical Research
    Coordinators
  • Telemedicine PIs
  • Home-based logistics
    management
  • Mobile phlebotomy/
    mobile nursing
  • Access to patients in
    any location

Clinical Trial Software

  • ePRO/eCOA
  • eConsent
  • Telemedicine
  • Reminders/notifications
  • Real-time Data Analytics
  • EDC
Let's work together

Chat with one of our LTFU study experts

Take the first step to more efficient and inclusive clinical trials.

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94103-3627, United States
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