Clinical trial registry record

Efficacy and Safety of Aflibercept in Patients With Neovascular Age-related Macular Degeneration

A registered PHASE3 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Completed.
Evidence
Registered phase 3 study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated February 14, 2023.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05587062
Last registry update
February 14, 2023
Status
Completed
Phase
Phase 3
Sponsor
Cinnagen
Enrollment
168
Countries
Iran
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered PHASE3 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase 3
Study design
RANDOMIZED · PARALLEL · TREATMENT · QUADRUPLE
Evidence population
Human clinical study registration
Participants
168
Population
ALL · 55 Years to 80 Years
Duration
2019-10-01 to 2022-07-31
Intervention
Aflibercept (CinnaGen Co, Iran); Aflibercept (Regeneron, USA)
Comparator
Aflibercept (Regeneron, USA)
Outcomes measured
The proportion of patients achieving maintaining vision at week 52 — At week 52; Mean changes in the Best-Corrected Visual Acuity Index from week 0 to week 52 — Baseline and at week 52; The percentage of patients who have increase of ≥15 score in ETDRS at week 52 compared to week 0 — Baseline and at week…; The mean change in National Eye Institute Visual Function Questionnaire (NEI VFQ-25) at week 52 compared to week 0 — Ba…; Mean changes in central retinal thickness at week 52 compared to the screening visit — Baseline and at week 52; The percentage of patients without intra-retinal fluid and subretinal fluid at week 52 — Baseline and at week 52; Number of participants with Adverse Events (AEs) — Baseline up to Week 52
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase 3A trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Vision ageing · 100%Title contains controlled term: age-related macular degeneration. Abstract contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Title supplies longevity context: age-related. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.