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Two initial faricimab loading doses in treatment-naive neovascular AMD

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514408-15-00
Enrollment
50
Registered
2024-10-14
Start date
2024-11-14
Completion date
Unknown
Last updated
2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neovascular age-related macular degeneration

Brief summary

Proportion of patients without disease activity at week 8.

Detailed description

Proportion of patients with a 4, 6, 8, 10, 12, 14 or 16 week treatment interval between the 2nd faricimab loading dose and the 3rd faricimab injection., Change in best corrected visual acuity from baseline to week 4 and 8., Change in central subfield thickness from baseline to week 4 and 8., Characteristics/measurements (in optical coherence tomography (OCT), optical coherence tomography angiography (OCTA), angiography and best corrected visual acuity (BCVA) assessment), which can predict active/non-active disease.

Interventions

Sponsors

Medical University Of Graz
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Proportion of patients without disease activity at week 8.

Secondary

MeasureTime frame
Proportion of patients with a 4, 6, 8, 10, 12, 14 or 16 week treatment interval between the 2nd faricimab loading dose and the 3rd faricimab injection., Change in best corrected visual acuity from baseline to week 4 and 8., Change in central subfield thickness from baseline to week 4 and 8., Characteristics/measurements (in optical coherence tomography (OCT), optical coherence tomography angiography (OCTA), angiography and best corrected visual acuity (BCVA) assessment), which can predict active/non-active disease.

Countries

Austria

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026