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Terminated Phase 1Phase 2 Interventional Results available

Safety and Bioactivity of AXT107 in Subjects With Diabetic Macular Edema

ClinicalTrials.gov ID: NCT04697758

Public ClinicalTrials.gov record NCT04697758. 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 Oct 26, 2026, 3:04 PM EDT

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

Official title

Phase 1/2a Study of the Safety and Bioactivity of AXT-107 in Subjects With Diabetic Macular Edema (DME)

Brief summary

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

This study is an open-label, dose-escalating, 48-week study assessing the safety, tolerability, bioactivity and duration of action of a single intravitreal injection of 0.1 mg, 0.25 mg, or 0.5 mg AXT107 in approximately 18 subjects (up to 6 subjects per dose) with Diabetic Macular Edema (DME).

Study identification

NCT ID
NCT04697758
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AsclepiX Therapeutics, Inc.
Industry
Enrollment
6 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Dec 10, 2020 (Actual)
Primary completion
Oct 1, 2022 (Actual)
Completion
Oct 1, 2022 (Actual)
Last update posted
Mar 22, 2024

2020 – 2022

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
AsclepiX Investigative Site Gilbert Arizona 85053 —
AsclepiX Investigative Site Los Angeles California 90211 —
AsclepiX Investigative Site St. Petersburg Florida 33711 —
AsclepiX Investigative Site Boston Massachusetts 02114 —
AsclepiX Investigative Site Reno Nevada 89502 —
AsclepiX Investigative Site Eugene Oregon 97401 —
AsclepiX Investigative Site Philadelphia Pennsylvania 19107 —
AsclepiX Investigative Site Abilene Texas 79606 —
AsclepiX Investigative Site McAllen Texas 78550 —
AsclepiX Investigative Site 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04697758, 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 Mar 22, 2024 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04697758 live on ClinicalTrials.gov.

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