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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04527107
Other study ID # THR-149-002
Secondary ID 2019-001506-17
Status Completed
Phase Phase 2
First received
Last updated
Start date July 31, 2020
Est. completion date November 22, 2023

Study information

Verified date November 2023
Source Oxurion
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Part A of the study is conducted to select the THR-149 dose level. Part B of the study is conducted to assess the efficacy and safety of the selected dose level compared to aflibercept, up to Month 3. As from Month 3, in about half of the subjects, the effect of a single flip-over injection (aflibercept or THR-149) will be evaluated when administered 1 month after the 3 monthly injections of THR-149 or aflibercept. In the other subjects, the durability of 3 monthly injections of THR 149 or aflibercept will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date November 22, 2023
Est. primary completion date September 28, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Key Inclusion Criteria: - Written informed consent obtained from the subject prior to screening procedures - Male or female aged 18 years or older at the time of signing the informed consent - Type 1 or type 2 diabetes - BCVA ETDRS letter score = 73 and = 39 in the study eye (for subjects in Part A); BCVA ETDRS letter score = 73 and = 24 in the study eye (for subjects in Part B) - Central involved DME (CI-DME) with CST of = 320µm in men or = 305µm in women, on spectral domain optical coherence tomography (SD-OCT), in the study eye - Received = 5 anti-vascular endothelial growth factor (anti-VEGF) injections for the treatment of CI-DME - BCVA ETDRS letter score = 34 in the fellow eye Key Exclusion Criteria: - Macular edema due to causes other than DME in the study eye - Concurrent disease in the study eye, other than central-involved DME, that could require medical or surgical intervention during the study period or could confound interpretation of the results - Any condition that could confound the ability to detect the efficacy of the investigational medicinal product - Previous confounding medications / interventions, or their planned administration - Presence of neovascularisation at the disc in the study eye - Presence of iris neovascularisation in the study eye - Uncontrolled glaucoma in the study eye - Any active or suspected ocular or periocular infection, or active intraocular inflammation, in either eye - Untreated Diabetes Mellitus - Glycated haemoglobin A (HbA1c) > 12% - Uncontrolled hypertension

Study Design


Intervention

Drug:
THR-149 dose level 1
3 intravitreal injections of THR-149 dose level 1, 1 month apart
THR-149 dose level 2
3 intravitreal injections of THR-149 dose level 2, 1 month apart
THR-149 dose level 3
3 intravitreal injections of THR-149 dose level 3, 1 month apart
THR-149 0.13mg
3 intravitreal injections of THR-149 0.13mg (selected dose level), 1 month apart, followed after 1 month by a sham (pretend) injection
THR-149 0.13mg + aflibercept 2mg
3 intravitreal injections of THR-149 0.13mg (selected dose level), 1 month apart, followed after 1 month by an intravitreal injection of aflibercept 2mg
aflibercept 2mg + THR-149 0.13mg
3 intravitreal injections of aflibercept 2mg, 1 month apart, followed after 1 month by an intravitreal injection of THR-149 0.13mg (selected dose level)
Aflibercept 2mg
3 intravitreal injections of aflibercept 2mg, 1 month apart, followed after 1 month by a sham (pretend) injection

Locations

Country Name City State
Czechia Všeobecná fakultní nemocnice v Praze Praha 2
France Centre Hospitalier Intercommunal de Créteil Créteil
France CHU de Dijon Dijon
France Hôpital de la Croix Rousse Lyon
France Centre Paradis Monticelli Marseille
France Fondation Rothschild Paris
France Hôpital Lariboisière Paris Cedex 10
Germany Universitätsklinikum Carl Gustav Carus Dresden Dresden
Germany Internationale Innovative Ophthalmochirurgie Düsseldorf
Germany Universitätsklinikum Frankfurt Frankfurt am Main
Germany Universitätsmedizin Göttingen Göttingen
Germany Universitätsklinikum Hamburg-Eppendorf Hamburg
Germany Universitätsklinikum Regensburg Regensburg
Italy IRCCS Ospedale San Raffaele Milan
Italy IRCCS Fondazione G.B. Bietti Roma
Italy Azienda Sanitaria Universitaria Friuli Centrale Udine
Slovakia Fakultná nemocnica s poliklinikou Žilina Žilina
Spain Hospital de la Esperanza Barcelona
Spain Hospital Dos de Maig Barcelona
Spain Hospital General de Catalunya Barcelona
Spain Hospital Universitari de Bellvitge Barcelona
Spain Instituto Clínico Quirúrgico de Oftalmología Bilbao
Spain METAVISIÓN ARRUZAFA, S.L.Clínica de Oftalmología de Córdoba S.L. (Hospital La Arruzafa) Córdoba
Spain Hospital Universitario Puerta de Hierro Majadahonda Madrid
Spain Instituto Oftalmológico Gómez-Ulla Santiago De Compostela
Spain Hospital Universitario Virgen Macarena Sevilla
Spain Fundación de Oftalmología Médica de la Comunitat Valenciana Valencia
Spain Hospital Universitario Rio Hortega Valladolid
Spain Hospital Clínico Universitario Lozano Blesa Zaragoza
United Kingdom University Hospitals Bristol NHS Foundation Trust Bristol
United Kingdom Kent and Canterbury Hospital Canterbury
United Kingdom Frimley Health NHS Foundation Trust Frimley
United Kingdom King's College Hospital NHS Foundation Trust London
United Kingdom London North West University Healthcare NHS Trust London
United Kingdom Moorfields Eye Hospital NHS Foundation Trust London
United Kingdom South Tyneside and Sunderland NHS Foundation Trust Sunderland
United Kingdom Mid and South Essex NHS Foundation Trust Westcliff-on-Sea
United States Retina Research Institute of Texas Abilene Texas
United States Southeast Retina Center Augusta Georgia
United States Austin Research Center for Retina Austin Texas
United States Austin Retina Associates Austin Texas
United States Retina Research Center, PLLC Austin Texas
United States Retina-Vitreous Associates Medical Group Beverly Hills California
United States Joslin Diabetes Center Boston Massachusetts
United States Cincinnati Eye Institute Cincinnati Ohio
United States Blue Ocean Clinical Research Clearwater Florida
United States Retina Associates of Cleveland, Inc Cleveland Ohio
United States University Hospitals Cleveland Medical Center Cleveland Ohio
United States Retina Consultants of Southern Colorado, P.C. Colorado Springs Colorado
United States Texas Retina Associates Dallas Texas
United States Henry Ford Hospital Detroit Michigan
United States Sterling Vision, P.C. dba Oregon Retina Eugene Oregon
United States Cumberland Valley Retina Consultants Hagerstown Maryland
United States Houston Eye Associates Houston Texas
United States Retina Consultants of Houston, PA Houston Texas
United States Salehi Retina Institute Inc. Huntington Beach California
United States Retina-Vitreous Surgeons of Central New York, PC Liverpool New York
United States Piedmont Eye Center Lynchburg Virginia
United States Marietta Eye Clinic Marietta Georgia
United States Valley Retina Institute, PA McAllen Texas
United States WVU Eye Institute Morgantown West Virginia
United States Northern California Retina Vitreous Associates Medical Group, Inc. Mountain View California
United States Tenneesse Retina Nashville Tennessee
United States Wagner Macula & Retina Center Norfolk Virginia
United States University Retina and Macula Associates, PC Oak Forest Illinois
United States California Retina Consultants Oxnard California
United States Retinal Research Institute, LLC Phoenix Arizona
United States Fort Lauderdale Eye Institute Plantation Florida
United States Retina Consultants San Diego Poway California
United States Sierra Eye Associates Reno Nevada
United States Retinal Consultants Medical Group Sacramento California
United States Retina Associates of Utah Salt Lake City Utah
United States Medical Center Ophthalmology Associates San Antonio Texas
United States Retina Associates of South Texas, P.A. San Antonio Texas
United States Retina Consultants of Texas San Antonio Texas
United States MedEye Associates South Miami Florida
United States Retina Associates Tucson Arizona
United States Center for Retina and Macular Disease Winter Haven Florida

Sponsors (1)

Lead Sponsor Collaborator
Oxurion

Countries where clinical trial is conducted

United States,  Czechia,  France,  Germany,  Italy,  Slovakia,  Spain,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean change in best-corrected visual acuity (BCVA) ETDRS letter score from Baseline, in subjects in Part B of the study At Month 3
Secondary Mean change in BCVA ETDRS letter score from Baseline, by study visit Up to Month 6
Secondary Mean change in central subfield thickness (CST) from Baseline, by study visit Up to Month 6
Secondary Incidence of systemic and ocular adverse events (AEs) and serious adverse events (SAEs) Up to Month 6
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