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Not yet recruitingNCT07728981Updated Jul 27, 2026

Biomarkers, Effectiveness, and Safety of Aflibercept 8mg Modified Fixed Dose Regimen in Treatment-Naïve nAMD Patients

An Early Phase 1 interventional study of Aflibercept 8mg in Neovascular Age-Related Macular Degeneration (nAMD) Wet AMD, sponsored by Tianjin Medical University Eye Hospital. Not yet recruiting. Open to participants aged 50 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-07-27.

Sponsored by Tianjin Medical University Eye Hospital · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
49
Allocation
Not applicable
Ages
50 Years to 85 Years
Sex
All
01

Study summary

Primary objective:

  • To evaluate the change in aqueous humor vascular endothelial growth factor A (VEGF-A) levels after 2 months of initial treatment with 8 mg Aflibercept in treatment-naïve nAMD patients.

Secondary objectives:

  • To assess the efficacy, safety, and biomarker changes of 8 mg Aflibercept using a modified fixed-interval dosing regimen over 12 months in treatment-naïve nAMD patients.
Read the detailed description

Age-related macular degeneration (AMD) is a disease that affects the central part of the retina (the macula) and can lead to loss of central vision in older adults. In developed countries, this condition is the leading cause of central vision loss in this population. AMD has two clinical subtypes: dry and wet (neovascular) forms. The dry type is characterized by progressive accumulation of drusen, with secondary degeneration of the retinal pigment epithelium and photoreceptors; the wet type is characterized by retinal edema and neovascularization, which can lead to severe vision loss. Wet AMD is the main cause of most AMD-related blindness cases.

Inhibiting vascular endothelial growth factor (VEGF) activity with medication has been proven to be an effective therapeutic strategy for treating nAMD. In addition to Eylea® (Aflibercept) injection, multiple anti-VEGF drugs have been approved for nAMD treatment in various countries globally, such as Lucentis® (Ranibizumab), Conbercept, and Faricimab (Vabysmo®). Most nAMD patients require long-term chronic treatment. Although globally approved intravitreal (IVT) anti-VEGF therapies are effective and well tolerated, the need for frequent IVT injections (especially during the maintenance phase) places a significant burden on physicians, patients, and caregivers.

Currently, in China, local reimbursement policies for nAMD cover nine anti-VEGF injections, and patients must bear the cost for any additional treatments. As a chronic progressive disease, nAMD patients typically require longer-term management and more anti-VEGF therapies. Limitations in insurance reimbursement are a primary obstacle in clinical practice.

At the same time, anti-VEGF therapy requires a three-dose loading regimen (once per month), with frequent follow-up and a complex injection schedule, which imposes a significant financial burden on patients, increases treatment costs for physicians, results in low patient adherence, and ultimately reduces long-term visual benefits. A result from the Barometer global survey indicated that 95.2% of physicians and 83.9% of patients believe that improving the predictability of injection timing is the main direction for enhancing patient care.

02

Conditions studied

  • Neovascular Age-Related Macular Degeneration (nAMD) Wet AMD

Keywords

  • Neovascular Age-Related Macular Degeneration
  • Aflibercept 8mg
  • Modified Fixed Dose Regimen
03

In context

Macular Degeneration

1,459 studies on the registry are indexed under Macular Degeneration; 238 are open to participants now.

This study's planned enrollment of 49 is below the median of 56 across 985 interventional studies indexed under Macular Degeneration.

Browse Macular Degeneration studies →

Lead sponsor

Tianjin Medical University Eye Hospital is the lead sponsor of 18 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  1. Patients who fully understand the content, procedures, and possible adverse events (AEs) of this study and are able to provide written ;
  2. Male or female patients aged ≥50 years at the time of signing the informed consent;
  3. Women of (WOCBP) must agree to use dual during the study and for 4 months after discontinuation of study treatment, consisting of one medically recognized contraceptive method with a failure rate of less than 1% per year (see Appendix 1 for Contraceptive Measures, Definitions and Requirements for Women of Childbearing Potential) combined with a barrier method (e.g., condom). Women who have undergone surgical sterilization (such as hysterectomy, bilateral oophorectomy, or bilateral tubal ligation) or menopause for more than 1 year are considered not of childbearing potential. Women of childbearing potential must have a negative pregnancy test at screening and must not become pregnant, breastfeed, lactate, or plan pregnancy, breastfeeding, or egg donation during the study and for 4 months after discontinuation of study treatment;
  4. Male subjects whose partners are of childbearing potential must agree to use dual contraception during the study and for 4 months after the end of treatment, consisting of one medically recognized contraceptive method with a failure rate of less than 1% per year (see Appendix 1 for Contraceptive Measures, Definitions and Requirements for Women of Childbearing Potential) combined with a barrier method (e.g., condom), and must agree not to donate sperm during the study and for 4 months after the end of treatment.

    Inclusion Criteria for Study Eye

    Subjects included in this study must meet all of the following ocular inclusion criteria for the study eye:

  5. Have sufficiently clear ocular media and adequately dilated pupils to obtain high-quality retinal images for diagnosis;
  6. Untreated nAMD with active subfoveal choroidal neovascularization (CNV), with total CNV area accounting for more than 50% of the total lesion area.
  7. SD-OCT examination showed the presence of intraretinal fluid (IRF) and/or subretinal fluid (SRF) in the foveal center of the retina.
  8. During the screening and baseline periods, BCVA scores measured using the ETDRS visual acuity chart at an initial testing distance of 4 meters ranged from 78 to 24 ETDRS letters (inclusive) (approximately equivalent to Snellen visual acuity 20/32 to 20/320), and the vision loss was caused by nAMD.

Exclusion Criteria:

  1. Patients who have received other treatments (including anti-VEGF, , laser photocoagulation treatments [panretinal photocoagulation or macular photocoagulation], and photodynamic therapy [PDT]) or approved nAMD drugs/therapies;
  2. Patients with allergies or reactions to any component/ of the investigational product;
  3. Uncontrolled hypertension (defined as systolic blood pressure >160 mmHg or diastolic blood pressure >95 mmHg). Subjects may be treated with up to three known antihypertensive drugs to achieve adequate blood pressure control. This restriction applies to drugs that can be used for treating hypertension, even if the primary purpose of taking the drug for the subject is not blood pressure control. Any medication known to affect blood pressure must have a stable regimen for 12 weeks prior to screening;
  4. History of other diseases, metabolic dysfunctions, abnormal physical examinations, or clinical laboratory abnormalities that reasonably suggest a to the investigational drug, may interfere with the interpretation of study results, or could place the patient at high risk for treatment-related complications;
  5. Any condition that, in the opinion of the investigator, may affect the patient's ability to provide informed consent, comply with the study protocol, complete the study according to study procedures, or for which the patient's participation may affect the study results or their own safety; Exclusion criteria for study eye
  6. Any eye with diabetic retinopathy (DR), diabetic macular edema (DME), or any retinal vascular disease other than nAMD;
  7. Presence of extraocular/periocular infection or inflammation in any eye during the screening or baseline period;
  8. Presence of retinal pigment epithelium (RPE) tear or rupture, scarring, fibrosis, or atrophy involving the fovea;
  9. Fluorescein angiography (FA)/fundus photography (FP) showing:

    1. Total lesion area (including hemorrhage, scarring, and neovascularization) greater than 12 disc areas (30.5 mm²);
    2. Fibrosis or atrophy >50% of the total lesion area, and/or involving the fovea.
  10. Any intraocular disease that the investigator believes may reduce vision improvement or require medical or surgical intervention during the study (such as amblyopia, aphakia, retinal detachment, cataract, diabetic retinopathy or maculopathy, epiretinal membrane with traction):

    1. Presence of vitreous hemorrhage during the screening or baseline period;
    2. Uncontrolled glaucoma (intraocular pressure still >25 mmHg despite anti-glaucoma medication);
    3. Any cataract surgery or treatment for cataract surgery complications with steroids or yttrium-aluminum garnet (YAG) laser capsulotomy within 3 months prior to Day 1 of the study;
    4. Any prior intraocular surgery (e.g., vitrectomy, glaucoma surgery, corneal transplantation, or radiation therapy);
    5. Prior periocular or intravitreal drug injections (including anti-VEGF agents) for other retinal diseases;
    6. Presence of intraocular inflammation/infection in any eye within 12 weeks prior to the screening visit;
    7. History of idiopathic or -related uveitis in the study eye.
Terms in these criteria, in plain language(9)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
49 participants (estimated)

Study arms

  • Experimental
    Treatment-Naïve Patients With nAMD

    Treatment-Naïve Patients With Neovascular Age-Related Macular Degeneration

    Drug: Aflibercept 8mg

Interventions

  • All treatment-naïve nAMD patients who have completed screening and meet the eligibility criteria will be included in this study. Aflibercept 8 mg will be administered at Month 0, Month 2, Month 5, Month 8, and Month 11. A rescue treatment follow-up will be conducted at Month 1, and if the criteria for rescue treatment are met, one rescue treatment (Aflibercept 8 mg injection) will be given.

06

What researchers measure

Primary outcomes

  1. VEGF-A levels in the patient's aqueous humor

    In the second month, the average change in VEGF-A levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

Secondary outcomes

  1. Proportion of patients who did not receive remedial treatment

    Proportion of patients who did not receive remedial treatment within 12 months

    Time frame: From enrollment to the end of treatment at 12 months

  2. best corrected visual acuity (BCVA)

    At month 12, the changes in the patient's best corrected visual acuity (BCVA) relative to baseline

    Time frame: From enrollment to the end of treatment at 12 months

  3. central retinal thickness (CMT)

    At month 12, the changes in the patient's central retinal thickness (CMT) relative to baseline

    Time frame: From enrollment to the end of treatment at 12 months

  4. VEGF-B levels in the patient's aqueous humor

    In the second month, the average change in VEGF-B levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

  5. placental growth factor (PIGF) levels in the patient's aqueous humor

    In the second month, the average change in placental growth factor (PIGF) levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

  6. Ang-2 levels in the patient's aqueous humor

    In the second month, the average change in Ang-2 levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

  7. IL-6 levels in the patient's aqueous humor

    In the second month, the average change in IL-6 levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

  8. IL-8 levels in the patient's aqueous humor

    In the second month, the average change in IL-8 levels in the patient's aqueous humor relative to baseline

    Time frame: From enrollment to the end of treatment at 0 months、2months、5months、8months、11months

  9. Average number of doses in the 12th month

    Average number of doses in the 12th month

    Time frame: "From enrollment to the end of treatment at 12 months

  10. the average area/volume of macular neovascularization (MNV)

    At each key visit time point, the relative change from baseline in the average area/volume of macular neovascularization (MNV) in patients ...

    Time frame: From enrollment to the end of treatment at 0 month、2months、5months、8months、11months

  11. intraretinal fluid (IRF) or subretinal fluid (SRF) in the foveal area

    Percentage of patients with no intraretinal fluid (IRF) or subretinal fluid (SRF) in the foveal area at months 0, 2, and 12

    Time frame: From enrollment to the end of treatment at 2months、12months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jul 2026; primary completion for Aug 2026, 0 months later.

Of 75 phase 1 interventional studies under Macular Degeneration, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 30. This study's planned 0 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 1, 2026
First posted
Jul 27, 2026
StartEst.
Jul 25, 2026
Primary completionEst.
Aug 15, 2026
CompletionEst.
Dec 31, 2027
Last update
Jul 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07728981
Lead sponsor
Tianjin Medical University Eye Hospital
Collaborators
Hebei General Hospital, Shijiazhuang People's Hospital, The Affiliated Hospital of Inner Mongolia Medical University, Shanxi Eye Hospital
Responsible party
Li Xiaorong (professor, Tianjin Medical University Eye Hospital) — Principal investigator
First posted
Jul 27, 2026
Start date
Jul 25, 2026 (estimated)
Primary completion
Aug 15, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jul 27, 2026

Study contacts

Xinjun Ren, PHD
Contact
zlrxjrsy@126.com
+86 13902067301
Shoukuan Liu, master
Contact
lsk1530407426@126.com
17694924913

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Aflibercept

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