For Sponsors & CROs
ActagenCT offers sponsors and contract research organizations (CROs) rapid activation timelines, purpose-built infrastructure, and a Principal Investigator with experience on more than 100 NMD trials and direct relationships across the biotech and pharmaceutical industries.
Patients enrolled across our Principal Investigator's career in NMD research.
Target from agreement to enrollment-ready.
What We Provide
We manage the full lifecycle of a study — regulatory submissions, screening, enrollment, study visits, safety monitoring, data collection and close-out — overseen by a Principal Investigator with experience overseeing 100+ NMD trials.
Hands-on support at every stage: explaining what to expect, coordinating visit schedules, meeting accessibility needs, and staying available throughout participation.
Gait analysis, functional motor evaluations, respiratory measurements and disease-specific rating scales, performed by staff trained in the methodologies these trials demand.
Accelerated activation timelines, continuous FDA inspection readiness, and a patient-centered operating model that drives enrollment and retention.
Relationships with the neuromuscular clinical community and patient advocacy organizations, supporting recruitment into specialized studies.
We support programs across phases and study designs in neuromuscular research.
Discuss a studyOur Facility
The ActagenCT center in Dublin, California is purpose-built for NMD patients and their families.
Full wheelchair accessibility throughout.
Purpose-built assessment areas for specialized NMD evaluations.
Comfortable, welcoming spaces for caregivers and family members.
Dublin, California — San Francisco Bay Area.
Near Stanford Tri-Valley Hospital for emergency admitting access.
Strong transportation connections for families traveling from a distance.