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Completed Phase 1Phase 2 Interventional Results available

A 2-part Study Consisting of Multiple Ascending Dose (MAD) Safety Study, and a Dose-finding Masked Study to Assess the Safety and Efficacy of Intravitreal (IVT) Remigromig (EYE103) in Patients With Diabetic Macular Edema (DME) or Neovascular Age-related Macular Degeneration (NVAMD)

ClinicalTrials.gov ID: NCT05919693

Public ClinicalTrials.gov record NCT05919693. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 3, 2026, 9:05 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 2-part Study Consisting of an Open-label Multiple Ascending Dose (MAD) Safety Study, and a Dose-finding Single-masked Comparative Safety and Preliminary Efficacy Study of Intravitreal (IVT) Remigromig in a Mixed Population of Participants With Diabetic Macular Edema (DME) or Neovascular Age-related Macular Degeneration (NVAMD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

EYE103-101 is a 2-part study assessing safety and preliminary efficacy of remigromig (EYE103) in patients with diabetic macular edema (DME) given as monotherapy or neovascular macular degeneration (NVAMD) given in combination with anti-VEGF. In the first part, termed the multiple ascending dose (MAD) portion of study, the safety of remigromig will be assessed at escalating doses. Approximately 12 participants will be entered in this part of the study. In the second part of the study, called the dose finding part two doses of remigromig will be selected and their effectiveness will be compared. Approximately 80 participants will be entered in this part of the study.

Study identification

NCT ID
NCT05919693
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
EyeBiotech Ltd.
Industry
Enrollment
33 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 12, 2023 (Actual)
Primary completion
Aug 26, 2024 (Actual)
Completion
Aug 26, 2024 (Actual)
Last update posted
Nov 3, 2026

2023 – 2024

United States locations

U.S. sites
27
U.S. states
10
U.S. cities
26
Facility City State ZIP Site status
Phoenix, AZ Phoenix Arizona 85032 —
Bakersfield, CA Bakersfield California 93309 —
Modesto, CA Modesto California 95356 —
Mountain View, CA Mountain View California 94040 —
Sacramento, CA Sacramento California 95825 —
Sacramento, CA Sacramento California 95841 —
Colorado Springs, Colorado Colorado Springs Colorado 80909 —
Lakewood, CO Lakewood Colorado 80288 —
Pompano Beach Pompano Beach Florida 33064 —
Lemont, NV Lemont Illinois 60439 —
Hagerstown, MD Hagerstown Maryland 21740 —
Reno, NV Reno Nevada 89502 —
West Columbia, SC West Columbia South Carolina 29169 —
Germantown, TN Germantown Tennessee 38138 —
Knoxville, TN Knoxville Tennessee 37922 —
Nashville, TN Nashville Tennessee 37203 —
Abilene, TX Abilene Texas 79606 —
Amarillo, TX Amarillo Texas 79109 —
Austin, TX Austin Texas 78705 —
Bellaire, TX Bellaire Texas 77401 —
Dallas, TX Dallas Texas 75231 —
Katy, TX Katy Texas 77494 —
McAllen, TX McAllen Texas 78503 —
Plano, TX Plano Texas 75075 —
Round Rock, TX Round Rock Texas 78681 —
San Antonio, TX San Antonio Texas 78240 —
The Woodlands, TX The Woodlands Texas 77384 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05919693, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 3, 2026 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05919693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →