Last reviewed · How we verify

NCT05172401

Oxulumis®, Suprachoroidal Drug Administration of Triesence® in Diabetic Macular Edema

Withdrawn NA Last updated 13 January 2023
What this trial tests

NA trial testing Oxulumis® suprachoroidal microcatheterization administration of Triesence® in Diabetic Macular Edema. Withdrawn.

Timeline
15 September 2022
Primary endpoint
31 January 2023
31 January 2023

Quick facts

Lead sponsorOxular Limited
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date15 September 2022
Primary completion31 January 2023
Estimated completion31 January 2023

Drugs / interventions tested

Conditions studied

Sponsor

Oxular Limited — full company profile →

Who can join

18 and older, any sex, with Diabetic Macular Edema. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this clinical investigation is to evaluate the safety and tolerability of using the Oxulumis® microcatheterization device to administer Triesence® to the suprachoroidal space in participants with DME.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Diabetic Macular Edema

Currently open trials in the same condition.

Other Oxular Limited trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05172401.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing