A Study to Investigate the Efficacy and Safety of RG7774 in Patients With Diabetes Mellitus Type 1 or Type 2 With Treatment-Naive Diabetic Retinopathy (CANBERRA)

Roche

Status and phase: Completed; Phase 2

Conditions: Diabetic Retinopathy

Treatments: Drug: Placebo; Drug: RG7774

Study type: Interventional

Funder types: Industry

Identifiers

NCT04265261

2019-002067-10 (EudraCT Number)

BP41321

Details and patient eligibility

About

The study's main purpose is to asses the safety, tolerability, and effect of oral administration of RG7774 on the severity of diabetic retinopathy (DR) in participants with moderately severe to severe non-proliferative diabetic retinopathy (NPDR) and good vision.

Enrollment: 139 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

• Able and willing to provide written informed consent and to comply with the study protocol according to International Conference of Harmonization (ICH) and local regulations
• Male and female patients of at least 18 years of age
• Treatment naïve with moderately severe to severe NPDR defined as ETDRS DRSS 47 or 53
• Patients are eligible with and without DME in either eye
• BCVA score at screening of at least 70 letters in study eyes without DME and at least 75 letters in case DME is present
• Clear ocular media and adequate pupillary dilation to allow acquisition of good quality retinal images.
• Diagnosis of diabetes mellitus (DM) type 1 or type 2
• Hemoglobin A1c (HbA1c) </= 12%.
• A female is eligible to participate if she is not pregnant, not breastfeeding

Exclusion Criteria

Ocular criteria for study eye:

• Prior treatment for DR or other retinal diseases with any approved or investigational therapy, including but not limited to intravitreal steroids, intravitreal anti-VEGF, light therapy, periocular pharmacological intervention, and laser (e.g. focal, grid, micropulse, or pan-retinal)
• Uncontrolled glaucoma
• Any concurrent intraocular condition (e.g. retinal detachment, dense cataract, epiretinal membrane with traction, or vitreomacular traction, etc.) that in the opinion of the Investigator could reduce the potential for improvement, require medical surgical intervention or may confound the visual and functional assessment and interpretation of study results

Concurrent ocular conditions in either eye:

• Any active ocular infection
• Any active intraocular inflammation

General Criteria:

• Previous systemic use of anti-VEGF drugs within 6 months prior to screening
• Complications of diabetes such as end-stage renal disease or liver disease
• Currently untreated diabetes mellitus or previously untreated patients who initiated oral or injectable anti-diabetic medication within 3 months prior to screening
• Uncontrolled blood pressure ([BP] defined as systolic > 180mmHg and/or diastolic >100 mmHg while patient at rest)
• History of concurrent cardio-vascular disease not considered well controlled by the Investigator
• Any major illness or major surgical procedure within one month before screening
• History of or currently active other diseases, metabolic dysfunction, physical examination finding, malignancies not considered cured, or clinical laboratory findings giving reasonable suspicion of a condition that contraindicated the use of the investigational medicinal drug or that might affect interpretation of the results of the study or renders the patient at high risk for treatment complications in the opinion of the investigator
• Known hypersensitivity to any of the excipients of the drug used, fluorescein dye or dilating eye drops
• Use of systemic medications known to be toxic to the lens, retina or optic nerve (e.g., deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, phenothiazines and ethambutol) used during the 6-month period prior to screening or likely need to be used

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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139 participants in 3 patient groups, including a placebo group

Group A

Placebo Comparator group

Description:

Participants will receive an oral dose of placebo matched to RG7774 once daily (QD)

Treatment:

Drug: Placebo

Group B

Experimental group

Description:

Participants will receive a low oral dose of RG7774 QD

Treatment:

Drug: RG7774

Group C

Experimental group

Description:

Participants will receive a high oral dose of RG7774 QD

Treatment:

Drug: RG7774