Clinical trial • Phase I • Ophthalmology

DS101 for Diabetic retinopathy

Phase I trial of DS101 for Diabetic retinopathy. Randomised, placebo (dose/schedule not specified)-controlled. 12 participants.

Overview

Trial Therapeutic Area
Ophthalmology
Trial Disease
Diabetic retinopathy
Trial Stage
Phase I

Key dates

Initial CTIS Submission Date
19-12-2024
First CTIS Authorization Date
08-04-2025

Trial design

Randomised, placebo (dose/schedule not specified)-controlled Phase I trial across 1 site in Spain.

Randomised
Yes
Comparator
Placebo (dose/schedule not specified)
Single Multiple Or Escalation Dose Combined
Yes
Target Sample Size
12

Eligibility

Recruits 12 Vulnerable population not selected; trial population: Healthy volunteers. No specific consent or assent handling details provided in the record..

Vulnerable Population
Vulnerable population not selected; trial population: Healthy volunteers. No specific consent or assent handling details provided in the record.

Recruitment

Planned Sample Size
12
Recruitment Window Months
6

Geography

Total Number Of Sites
1
Total Number Of Participants
12

Spain

Earliest CTIS Part Ii Submission Date
12-03-2025
Latest Decision Or Authorization Date
08-04-2025
Processing Time Days
27
Number Of Sites
1
Number Of Participants
12

Sites

Site Name
Hospital Universitari Vall D Hebron
Department Name
Ophthalmology Service
Contact Person Name
Miguel Ángel Zapata

Sponsor

Primary sponsor

Full Name
Fundacio Hospital Universitari Vall D’Hebron Institut De Recerca
Organisation Type
Laboratory/Research/Testing facility
Country Of Registered Address
Spain

Investigational products

Investigational Product Name
DS101
Routes Of Administration
Topical ocular administration
Route
Topical ocular

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