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NCT03671135

Safety and Efficacy of an Intrastromal Transform™ Corneal Allograft (TCA) for Presbyopia Correction

Terminated NA Last updated 23 February 2024
What this trial tests

NA trial testing TCA Intrastromal Inlay in Presbyopia in 121 participants. Terminated before completion.

Timeline
9 August 2018
Primary endpoint
31 December 2021
31 December 2021

Quick facts

Lead sponsorAllotex, Inc.
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment121
Start date9 August 2018
Primary completion31 December 2021
Estimated completion31 December 2021
Sites4 locations across Belgium, United Kingdom, Ireland

Drugs / interventions tested

Conditions studied

Sponsor

Allotex, Inc.

Who can join

Eligibility, any sex, with Presbyopia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this clinical study is to evaluate the safety and effectiveness of intrastromal implantation of the Allotex TransForm corneal allograft (TCA) for improving near vision in presbyopic subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Presbyopia

Currently open trials in the same condition.

Other Allotex, Inc. 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/NCT03671135.

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