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Terminated Phase 2 Interventional Results available

A Study to Assess the Safety, Tolerability and Effectiveness of MT-0814 for the Treatment of Age-related Macular Degeneration

ClinicalTrials.gov ID: NCT03869684

Public ClinicalTrials.gov record NCT03869684. 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 7, 2026, 2:21 PM EST

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Official title

A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety, Tolerability, and Efficacy of MT-0814 for the Treatment of Patients With Age-Related Macular Degeneration

Brief summary

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

Age-related macular degeneration (AMD) is the leading cause of blindness among adults in North America. The current standard of care for patients with exudative ("wet") AMD is anti-vascular endothelial growth factor (anti-VEGF) therapy which must be administered by an injection into the eye every 4-8 weeks. MT-0814 is being developed for the treatment of patients with exudative AMD, and could offer an alternative, safer and less burdensome therapy.

Study identification

NCT ID
NCT03869684
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Senju Pharmaceutical Co., Ltd.
Industry
Enrollment
13 participants

Conditions and interventions

Interventions

Drug

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
Feb 25, 2019 (Actual)
Primary completion
Mar 25, 2020 (Actual)
Completion
Apr 24, 2020 (Actual)
Last update posted
Apr 20, 2021

2019 – 2020

United States locations

U.S. sites
13
U.S. states
5
U.S. cities
13
Facility City State ZIP Site status
Senju Investigational Site Peoria Arizona 85381 —
Senju Investigational Site Phoenix Arizona 85053 —
Senju Investigational Site Pasadena California 91107 —
Senju Investigational Site Redlands California 92374 —
Senju Investigational Site Altamonte Springs Florida 32701 —
Senju Investigational Site Clearwater Florida 33761 —
Senju Investigational Site Melbourne Florida 32901 —
Senju Investigational Site Tallahassee Florida 32308 —
Senju Investigational Site Arlington Texas 76012 —
Senju Investigational Site Houston Texas 77030 —
Senju Investigational Site San Antonio Texas 78240 —
Senju Investigational Site The Woodlands Texas 77384 —
Senju Investigational Site Murray Utah 84107 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03869684, 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 Apr 20, 2021 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03869684 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →