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Topical Ocular Mecamylamine in Diabetic Macular Edema (DME)

C

CoMentis

Status and phase

Completed
Phase 2

Conditions

Diabetic Macular Edema

Treatments

Drug: mecamylamine

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00536692
ATG003-202

Details and patient eligibility

About

This is an open-label study evaluating the safety and tolerability of topical ocular mecamylamine given twice a day in patients with diabetic macular edema (DME). Patients will be treated for 12 weeks.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • macular edema due to diabetic retinopathy

Exclusion criteria

  • vision loss from other ocular disease
  • intraocular surgery within 3 months
  • intraocular anti-VEGF or steroids within 3 months
  • HbA1c >12

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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