MedPath

Intravitreal Aflibercept as Indicated by Real-Time Objective Imaging to Achieve Diabetic Retinopathy Improvement

Phase 2
Completed
Conditions
Diabetic Retinopathy
Interventions
Registration Number
NCT03531294
Lead Sponsor
Greater Houston Retina Research
Brief Summary

The PRIME trial will assess the safety of 2 mg intravitreal aflibercept injections (IAI) to achieve and maintain DRSS improvements (2 or more steps) in patients with a baseline DRSS level of 47A to 71A inclusive through 104 weeks as determined by reading center determined DRSS gradings on OPTOS fundus photos and leakage index on OPTOS WF-FA.

Detailed Description

Study eyes will be assigned randomly (1:1 ratio) to one of the following 2 treatment arms. Randomization of PDR subjects will be limited to 50% of each arm.

Group 1

Year 1 Subjects will be seen every month, 28 days (+ 7 days), for 52 weeks. All subjects will receive IAI at baseline, after eligibility is confirmed. Week 4 through week 48, subjects will be seen monthly and treated with IAI PRN (pro re nata) according to, same day, central reading center (CRC) determined DRSS level. Monthly treatment with IAI will continue until a greater than or equal to 2 step DRSS level improvement is achieved, relative to screening/baseline DRSS based on CRC assessment OPTOS fundus photos (FP). Subjects who have baseline proliferative diabetic retinopathy (PDR) (DRSS Level 61-71) will continue to receive monthly IAI until a greater than or equal to 2 step DRSS improvement is achieved as determined by CRC assessment of OPTOS fundus photos relative to screening/baseline DRSS, and PDR is quiescent according to the treating investigator. Treatment with IAI will be reinitiated if a 1 step worsening of DRSS occurs compared to best DRSS score achieved, determined by CRC evaluation of OPTOS fundus photos. If such worsening is detected, the subject would resume monthly IAI until best DRSS score or greater is achieved, as determined by CRC assessment of OPTOS fundus photos. In addition, retreatment will also be re-started if new onset neovascularization is identified and is continued until the PDR is quiescent according to the treating investigator.

Year 2 Beginning in year 2 (week 52) subjects will be seen every 56 days (+ 14 days) and treated with IAI PRN (pro re nata) utilizing the same criteria from year 1. All subjects will have a mandatory week 104 visit, where treatment will not be given.

Group 2

Year 1 Subjects will be seen every month, 28 days (+ 7 days), for 52 weeks. All subjects will receive IAI at baseline, after eligibility is confirmed. Week 4 through week 48, subjects will be seen monthly and treated with IAI PRN (pro re nata) according to, same day, CRC determination of DRSS initially, and subsequently of leakage index.

Monthly treatment with IAI will continue until a greater than or equal to 2 step DRSS level improvement is achieved, relative to screening/baseline DRSS based on CRC assessment OPTOS fundus photos (FP). Subjects who have baseline proliferative diabetic retinopathy (PDR) (DRSS Level 61-71) will continue to receive monthly IAI until a greater than or equal to 2 step DRSS improvement is achieved as determined by CRC assessment of OPTOS fundus photos relative to screening/baseline DRSS, and PDR is quiescent according to the treating investigator.

Leakage index as determined by CRC assessment of OPTOS WF-FA at the visit at which a greater than or equal to 2 step DRSS level improvement is achieved will be considered the threshold. Treatment with IAI will be reinitiated if the leakage index increases to 33% above the individual subject threshold leakage index level as determined by CRC evaluation of OPTOS WF-FA. If such worsening is detected, the subject would resume monthly IAI until the threshold leakage index as determined by CRC assessment of OPTOS WF-FA is reached. In addition, retreatment will also be re-started if new onset neovascularization is identified and is continued until the PDR is quiescent according to the treating investigator.

Year 2 Beginning in year 2 (week 52) subjects will be seen every 56 days (+ 14 days) and treated with IAI PRN (pro re nata) utilizing the same criteria from year 1. All subjects will have a mandatory week 104 visit, where treatment will not be given.

If images of insufficient quality are unable to be obtained, in Group 1 or Group 2, subjects will undergo treatment with IAI at principal investigators discretion or designee.

Subjects can have both eyes in the study, if eligibility is met. If both eyes are eligible, one eye will be randomized to group 1 while the other is randomized to group 2. If only one eye is eligible IAI will be provided for the fellow eye as needed according to the treating investigator.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  1. Men or Women > 18 years of age with type 1 or II diabetes mellitus
  2. Diabetic Retinopathy, DRSS Level 47A to 71A, as assessed by CRC (enrollment of PDR levels will be limited to 50% of the total population)
  3. BCVA in the study eye better than 20/800
Exclusion Criteria
  1. Any prior systemic anti-VEGF treatment or IVT anti-search vascular endothelial growth factor (VEGF) treatment in the study eye within 24 weeks of screening/baseline

  2. Any intravitreal or peribulbar corticosteroids in the study eye within 12 weeks of screening/baseline

  3. Any prior treatment with Ozurdex or Iluvien in the study eye

  4. SD-OCT central subfield thickness (CST) > 320 µm in the study eye

  5. Central DME causing visual acuity loss, in which treatment can not be safely deferred for at least 6 months, in the investigator's judgment

  6. Current visually significant vitreous hemorrhage in the study eye. Vitreous hemorrhage is allowed as long as DRSS level is 71A or lower.

  7. History of panretinal photocoagulation (PRP) in the study eye

  8. History of vitrectomy surgery in the study eye

  9. Cataract surgery in the study eye within 8 weeks of screening/baseline

  10. Pregnant or breast-feeding women

  11. Sexually active men* or women of childbearing potential** who are unwilling to practiceadequate contraception during the study (adequate contraceptive measures include stable use of oral contraceptives or other prescription pharmaceutical contraceptives for 2 or more menstrual cycles prior to screening/baseline; intrauterine device [IUD]; bilateral tubal ligation; vasectomy; condom plus contraceptive sponge, foam, or jelly, or diaphragm plus contraceptive sponge, foam, or jelly).

    * Contraception is not required for men with documented vasectomy.

    ** Postmenopausal women must be amenorrheic for at least 52 weeks in order not to be considered of childbearing potential. Pregnancy testing and contraception are not required for women with documented hysterectomy or tubal ligation.

  12. If currently receiving diaylisis, must have started treatment more than 12 weeks prior to screening/baseline

  13. Uncontrolled blood pressure (defined as > 190/110 mm Hg systolic/diastolic, while seated)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group 1Aflibercept InjectionTreatment based on central reading center reading evaluation of DRSS (diabetic retinopathy severity scale) level based on OPTOS funds photos.
Group 2Aflibercept InjectionTreatment based on central reading center reading evaluation of DRSS (diabetic retinopathy severity scale) level based leakage index of OPTOS wide field fluorescein angiography.
Primary Outcome Measures
NameTimeMethod
Incidence of Adverse Events for diabetic retinopathy subjects who receive intravitreal Aflibercept104 weeks

Assess the safety of 2 mg intravitreal aflibercept injections (IAI) to achieve and maintain DRSS improvements (2 or more steps) in patients with a baseline DRSS level of 47A to 71A inclusive as determined by reading center determined DRSS gradings on OPTOS fundus photos and leakage index on OPTOS WF-FA

Secondary Outcome Measures
NameTimeMethod
Mean number of IAI (NPDR VS PDR)104 weeks

Mean number of IVT aflibercept Injections in eyes with baseline NPDR vs PDR through week 52

ETDRS-BCVA change104 weeks

Mean change in Early Treatment Diabetic Retinopathy Study best corrected visual acuity (ETDRS-BCVA)

Changes in Visual Function104 weeks

Changes in visual function outcomes as measured by National Eye Institute Visual Functioning Questionnaire (NEI-VFQ)

Correlation of DRSS and leakage index104 weeks

Correlation of reading-center determined DRSS level and leakage index to determine change in DR severity

Correlation between Reading Center DRSS Level and Physician determined DR severity104 weeks

Correlation of reading-center determined DRSS level and investigator-determined DR severity level based on ophthalmoscopic fundus examination (Physician determined DR severity level will be based on AAO (American Academy of Ophthalmology) simplified grading system: mild NPDR, moderate NPDR, Severe NPDR, low risk PDR, high risk PDR)

Number of IAI104 weeks

Mean and Median number of IVT aflibercept Injections (with and without IAI given for DME)

Change in microaneurysms104 weeks

Change in number of microaneurysms, assessed by wide-field fluorescein angiography

Change in CST104 weeks

Mean change in central subfield thickness (CST), as assessed by spectral Domain Optical coherence tomography (SD-OCT)

DRSS Change104 weeks

Changes in DRSS

Change in Non-Perfusion104 weeks

Change in area of retinal non-perfusion within the macula and periphery

Change in Vascular Leakage104 weeks

Change in relative area of vascular leakage on wide-field fluorescein angiography

DME development104 weeks

Percentage of subjects, who develop center-involving diabetic macular edema necessitating treatment compared to baseline

PDR Development104 weeks

Percentage of subjects, who develop a new PDR event compared to baseline

Cytokine Levels104 weeks

Corelation of cytokine levels in aqueous humor samples to clinical and imaging outcomes

Trial Locations

Locations (2)

Retina Consultants of Houston

🇺🇸

The Woodlands, Texas, United States

Retina Consultants of Houston/The Medical Center

🇺🇸

Houston, Texas, United States

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