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A Pivotal Safety and Efficacy Study of OCS-01 Eye Drops in Participants With Diabetic Macular Edema (DIAMOND 1)

O

Oculis

Status and phase

Active, not recruiting
Phase 3
Phase 2

Conditions

Diabetic Macular Edema

Treatments

Drug: Dexamethasone ophthalmic suspension (OCS-01)
Drug: Vehicle

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

The primary objective of this study is to evaluate the efficacy and safety of the topical ophthalmic administration of OCS- 01 as compared to Vehicle in participants with Diabetic Macular Edema (DME).

Full description

A Phase 2/3 Pivotal Double-masked, Randomized, Vehicle-controlled, 2 stage, Multicenter Study of the Efficacy and Safety of OCS-01 Eye Drops in Participants with Diabetic Macular Edema

Stage 1: To select a dose and dosing regimen for OCS-01 in participants with DME and evaluate the efficacy and safety of OCS-01 as compared to Vehicle in participants with DME.

Stage 2: To evaluate the efficacy and safety of OCS-01 as compared to Vehicle at Week 52 in participants with DME.

Enrollment

552 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (selection) - Stage 1:

  1. Have a signed informed consent form before any study-specific procedures are performed.
  2. Have DME with presence of intraretinal and/or subretinal fluid in the study eye, with central subfield thickness (CST) of ≥310 µm by SD-OCT at screening (Visit 1) (as assessed by an independent reading center).
  3. Have a documented diagnosis of type 1 or type 2 diabetes mellitus at Visit 1 (Screening).

Inclusion Criteria (selection) - Stage 2:

  1. Have a signed informed consent form before any study-specific procedures are performed.
  2. Have DME with presence of intraretinal and/or subretinal fluid in the study eye, with central subfield thickness (CST) of ≥310 µm by SD-OCT at screening (Visit 1) (as assessed by an independent reading center).
  3. Have a documented diagnosis of type 1 or type 2 diabetes mellitus prior to Visit 1 (Screening).

Exclusion criteria (selection) - Stage 1 and Stage 2:

  1. Have macular edema considered to be because of a cause other than DME.
  2. Have a decrease in BCVA because of causes other than DME.
  3. Have a known history of significant macular ischemia which would prevent gain in visual acuity in the study eye.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

552 participants in 2 patient groups, including a placebo group

OCS-01
Experimental group
Description:
dexamethasone ophthalmic suspension,1.5% \[15 mg/ mL\]
Treatment:
Drug: Dexamethasone ophthalmic suspension (OCS-01)
Vehicle Vehicle
Placebo Comparator group
Description:
Placebo is a Vehicle ophthalmic suspension of OCS-01
Treatment:
Drug: Vehicle

Trial contacts and locations

56

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Central trial contact

Oculis Study Leader

Data sourced from clinicaltrials.gov

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