Sponsored Programs Through Beacon Clinical Research
A centralized pathway for patient enrollment, compassionate use requests, physician coordination, observational study participation, and real-world outcome data collection.
One pathway, full lifecycle
Beacon Clinical Research supports sponsor-program patient intake, compassionate use coordination, observational study enrollment, physician documentation, and real-world evidence data collection — under one organized workflow.
Patients, caregivers, and physicians use the same intake and follow-up infrastructure. Validated outcome measures are captured at baseline, 1 month, and 3 months. TNF-alpha values, diagnosis-specific functional scores, caregiver narratives, safety events, and concomitant therapy changes feed structured real-world evidence reporting.
NCT07521384
Real World Outcomes of Intranasal MuSE Exosomes and Stem Cells in Neurological Regenerative Therapy
Who This Page Is For
Six audiences. Same pipeline. Different entry points.
Patients and caregivers
Begin intake, submit diagnosis information, upload medical records, complete outcome questionnaires, and request compassionate use review.
Physicians
Refer patients, support compassionate use documentation, review eligibility, and participate in observational study documentation.
Clinical research partners
Coordinate study enrollment, data collection, and longitudinal follow-up across treating sites.
Sponsor leadership
Review real-world evidence intake, enrollment progress, outcome data collection, and observational study operations.
Study coordinators
Manage participant timepoints, send follow-up questionnaires, track required outcome data, and flag missing measures.
Compassionate use applicants
Submit physician-supported compassionate use review requests with medical documentation upload.
Available Pathways
Pick the pathway that matches your role and goal.
Patient / Caregiver Enrollment
For patients or caregivers interested in submitting medical history, diagnosis information, treatment interest, and study questionnaire data.
Start Patient EnrollmentCompassionate Use Request
For patients or caregivers seeking physician-supported compassionate use access review within the program’s therapy pathway.
Request Compassionate Use ReviewPhysician Participation
For physicians interested in referring patients, supporting compassionate use documentation, reviewing eligibility, or participating in observational study documentation.
Physician ParticipationNCT07521384
Real World Outcomes of Intranasal MuSE Exosomes and Stem Cells in Neurological Regenerative Therapy.
Baseline · 1-month · 3-month. Primary analysis window: baseline to 3 months.
Supported Data Collection
Every category captured under one organized workflow.
Need help with enrollment?
Beacon's clinical operations team supports patients, caregivers, physicians, and study coordinators through every step — from initial intake through 3-month follow-up.
Prefer to start from your phone?
Verify your mobile number by text message and finish the patient intake at your own pace.