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A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00168389
Enrollment
494
Registered
2005-09-15
Start date
2005-02-28
Completion date
2012-06-30
Last updated
2014-08-04

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

Conditions

Diabetic Macular Edema

Brief summary

This study will evaluate the safety and efficacy of an intravitreal implant of dexamethasone for the treatment of diabetic macular edema.

Interventions

DRUGDexamethasone

350 µg or 700 µg dexamethasone posterior segment drug delivery system - injection into the vitreous cavity not less than every 6 months for up to 36 months.

OTHERSham

Sham posterior segment drug delivery system - needle-less drug delivery system without study medication not less than every 6 months for up to 36 months.

Sponsors

Allergan
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Key Inclusion Criteria: * 18 years of age or older with diabetic macular edema; * Decrease in visual acuity in at least one eye as a result of macular edema (20/50 or worse); * Visual acuity in other eye no worse than 20/200 Key

Exclusion criteria

* Known anticipated need for ocular surgery within first 12 months of study; * History of glaucoma or current high eye pressure requiring more than 1 medication; * Uncontrolled systemic disease; * Known steroid-responder; * Use of systemic steroids * Use of Warfarin/Heparin

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Patients With a Best Corrected Visual Acuity (BCVA) Improvement of ≥15 Letters From Baseline in the Study EyeBaseline, Month 39/Final VisitBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.

Secondary

MeasureTime frameDescription
Change From Baseline in BCVA in the Study EyeBaseline, Month 39/Final VisitBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). A positive number change from baseline indicates an improvement and a negative number change from baseline indicates a worsening.
Percentage of Patients With a BCVA Improvement of ≥10 Letters From Baseline in the Study EyeBaseline, Month 39/Final VisitBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.
Average Change From Baseline in BCVA in the Study EyeBaseline, 39 MonthsBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). The average BCVA is calculated across study visits for each patient. A positive number change from baseline indicates an improvement and a negative number change from baseline indicates a worsening.
10th Percentile for Time to BCVA Improvement of ≥15 Letters From Baseline in the Study EyeBaseline, 39 MonthsBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). Shorter durations of time to improvement are best. The 10th percentile represents the first 10% of patients to reach a BCVA improvement of ≥15 letters from baseline in the study eye.
Percentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsBaseline, Month 3, Month 6, Month 9, Month 12, Month 15, Month 18, Month 21, Month 24, Month 27, Month 30, Month 33, Month 36, Month 39/Final VisitBCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.
Average Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Baseline, 39 MonthsOCT is a laser-based, noninvasive, diagnostic system that provides high-resolution, three-dimensional images of the retina from which retinal thickness can be measured. The average OCT retinal thickness is calculated across study visits for each patient. A negative number change from baseline indicates an improvement and a positive number change from baseline indicates a worsening.

Countries

Australia, Canada, Czechia, Germany, Israel, Philippines, Portugal, South Africa, Spain, United States

Participant flow

Participants by arm

ArmCount
Dexamethasone 700 μg
700 µg Dexamethasone posterior segment drug delivery system - injection into the vitreous cavity not less than every 6 months for up to 36 months.
163
Dexamethasone 350 μg
350 µg Dexamethasone posterior segment drug delivery system - injection into the vitreous cavity not less than every 6 months for up to 36 months.
166
Sham
Sham posterior segment drug delivery system - needle-less drug delivery system without study medication not less than every 6 months for up to 36 months.
165
Total494

Baseline characteristics

CharacteristicTotalDexamethasone 700 μgDexamethasone 350 μgSham
Age, Customized
45 to 65 years
281 Participants89 Participants97 Participants95 Participants
Age, Customized
<45 years
16 Participants4 Participants5 Participants7 Participants
Age, Customized
>65 years
197 Participants70 Participants64 Participants63 Participants
Sex: Female, Male
Female
190 Participants61 Participants66 Participants63 Participants
Sex: Female, Male
Male
304 Participants102 Participants100 Participants102 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —
other
Total, other adverse events
153 / 160162 / 165124 / 164
serious
Total, serious adverse events
52 / 16052 / 16534 / 164

Outcome results

Primary

Percentage of Patients With a Best Corrected Visual Acuity (BCVA) Improvement of ≥15 Letters From Baseline in the Study Eye

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.

Time frame: Baseline, Month 39/Final Visit

Population: Intent to Treat: all randomized patients

ArmMeasureValue (NUMBER)
Dexamethasone 700 μgPercentage of Patients With a Best Corrected Visual Acuity (BCVA) Improvement of ≥15 Letters From Baseline in the Study Eye22.1 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With a Best Corrected Visual Acuity (BCVA) Improvement of ≥15 Letters From Baseline in the Study Eye18.7 Percentage of Patients
ShamPercentage of Patients With a Best Corrected Visual Acuity (BCVA) Improvement of ≥15 Letters From Baseline in the Study Eye13.3 Percentage of Patients
Secondary

10th Percentile for Time to BCVA Improvement of ≥15 Letters From Baseline in the Study Eye

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). Shorter durations of time to improvement are best. The 10th percentile represents the first 10% of patients to reach a BCVA improvement of ≥15 letters from baseline in the study eye.

Time frame: Baseline, 39 Months

Population: Intent to Treat: all randomized patients

ArmMeasureValue (NUMBER)
Dexamethasone 700 μg10th Percentile for Time to BCVA Improvement of ≥15 Letters From Baseline in the Study Eye50 Days
Dexamethasone 350 μg10th Percentile for Time to BCVA Improvement of ≥15 Letters From Baseline in the Study Eye51 Days
Sham10th Percentile for Time to BCVA Improvement of ≥15 Letters From Baseline in the Study Eye150 Days
Secondary

Average Change From Baseline in BCVA in the Study Eye

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). The average BCVA is calculated across study visits for each patient. A positive number change from baseline indicates an improvement and a negative number change from baseline indicates a worsening.

Time frame: Baseline, 39 Months

Population: Intent to Treat: all randomized patients

ArmMeasureGroupValue (MEAN)Dispersion
Dexamethasone 700 μgAverage Change From Baseline in BCVA in the Study EyeBaseline56.2 LettersStandard Deviation 10.5
Dexamethasone 700 μgAverage Change From Baseline in BCVA in the Study EyeAverage Change from Baseline Over 39 Months4.1 LettersStandard Deviation 8.26
Dexamethasone 350 μgAverage Change From Baseline in BCVA in the Study EyeBaseline55.9 LettersStandard Deviation 9.64
Dexamethasone 350 μgAverage Change From Baseline in BCVA in the Study EyeAverage Change from Baseline Over 39 Months4.3 LettersStandard Deviation 8.49
ShamAverage Change From Baseline in BCVA in the Study EyeBaseline56.8 LettersStandard Deviation 8.66
ShamAverage Change From Baseline in BCVA in the Study EyeAverage Change from Baseline Over 39 Months1.9 LettersStandard Deviation 7.74
Secondary

Average Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)

OCT is a laser-based, noninvasive, diagnostic system that provides high-resolution, three-dimensional images of the retina from which retinal thickness can be measured. The average OCT retinal thickness is calculated across study visits for each patient. A negative number change from baseline indicates an improvement and a positive number change from baseline indicates a worsening.

Time frame: Baseline, 39 Months

Population: Intent to Treat: all randomized patients with data at the time point

ArmMeasureGroupValue (MEAN)Dispersion
Dexamethasone 700 μgAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Baseline436.7 MicronsStandard Deviation 145.88
Dexamethasone 700 μgAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Average Change from Baseline Over 39 Months-101.1 MicronsStandard Deviation 119.17
Dexamethasone 350 μgAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Baseline457.4 MicronsStandard Deviation 158.09
Dexamethasone 350 μgAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Average Change from Baseline Over 39 Months-103.9 MicronsStandard Deviation 137.88
ShamAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Baseline468.7 MicronsStandard Deviation 129.61
ShamAverage Change From Baseline in Retinal Thickness as Measured by Optical Coherence Tomography (OCT)Average Change from Baseline Over 39 Months-37.8 MicronsStandard Deviation 103.96
Secondary

Change From Baseline in BCVA in the Study Eye

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). A positive number change from baseline indicates an improvement and a negative number change from baseline indicates a worsening.

Time frame: Baseline, Month 39/Final Visit

Population: Intent to Treat: all randomized patients

ArmMeasureGroupValue (MEAN)Dispersion
Dexamethasone 700 μgChange From Baseline in BCVA in the Study EyeBaseline56.2 LettersStandard Deviation 10.5
Dexamethasone 700 μgChange From Baseline in BCVA in the Study EyeChange from Baseline at Month 39/Final Visit4.1 LettersStandard Deviation 13.89
Dexamethasone 350 μgChange From Baseline in BCVA in the Study EyeBaseline55.9 LettersStandard Deviation 9.64
Dexamethasone 350 μgChange From Baseline in BCVA in the Study EyeChange from Baseline at Month 39/Final Visit5.0 LettersStandard Deviation 11.97
ShamChange From Baseline in BCVA in the Study EyeBaseline56.8 LettersStandard Deviation 8.66
ShamChange From Baseline in BCVA in the Study EyeChange from Baseline at Month 39/Final Visit0.8 LettersStandard Deviation 11.89
Secondary

Percentage of Patients With a BCVA Improvement of ≥10 Letters From Baseline in the Study Eye

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.

Time frame: Baseline, Month 39/Final Visit

Population: Intent to Treat: all randomized patients

ArmMeasureValue (NUMBER)
Dexamethasone 700 μgPercentage of Patients With a BCVA Improvement of ≥10 Letters From Baseline in the Study Eye38.7 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With a BCVA Improvement of ≥10 Letters From Baseline in the Study Eye34.3 Percentage of Patients
ShamPercentage of Patients With a BCVA Improvement of ≥10 Letters From Baseline in the Study Eye23.0 Percentage of Patients
Secondary

Percentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month Intervals

BCVA is measured using an eye chart and is reported as the number of letters read correctly (ranging from 0 to 100 letters) in the study eye. The lower the number of letters read correctly on the eye chart, the worse the vision (or visual acuity). An increase in the number of letters read correctly indicates improvement and a decrease in the number of letters read correctly indicates a worsening.

Time frame: Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, Month 18, Month 21, Month 24, Month 27, Month 30, Month 33, Month 36, Month 39/Final Visit

Population: Intent to Treat: all randomized patients

ArmMeasureGroupValue (NUMBER)
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3620.9 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2720.2 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1817.2 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 919.0 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2414.1 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2116.6 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 314.1 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 614.1 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3322.1 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1213.5 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 39/Final Visit22.1 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3016.6 Percentage of Patients
Dexamethasone 700 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1515.3 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2115.1 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 313.9 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 610.2 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 918.1 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1215.1 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1516.3 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 189.6 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2415.1 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2719.3 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3019.9 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3317.5 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3619.9 Percentage of Patients
Dexamethasone 350 μgPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 39/Final Visit18.7 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2712.7 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 129.1 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3612.7 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3011.5 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 98.5 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 36.1 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 3311.5 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 219.1 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 1810.9 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 67.9 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 2410.9 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 157.3 Percentage of Patients
ShamPercentage of Patients With BCVA Improvement of ≥15 Letters From Baseline in the Study Eye at 3-month IntervalsMonth 39/Final Visit13.3 Percentage of Patients

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026