Trials / Withdrawn
WithdrawnNCT03927443
A Comparative Study of SPARC's SDP-133 Once Daily and Lumigan in Subjects With Open Angle Glaucoma or Ocular Hypertension
A Multi-Center, Evaluator -Masked, Randomized, Parallel Group, Active Controlled, Comparative Study of SPARC's SDP-133 Once Daily Compared With Lumigan ® 0.01% (Bimatoprost Ophthalmic Solution) in Subjects With Open Angle Glaucoma or Ocular Hypertension
- Status
- Withdrawn
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Sun Pharmaceutical Industries Limited · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the efficacy of once daily dosing with SPARC's novel ophthalmic formulation of bimatoprost compared with Lumigan 0.01% in subjects with open-angle glaucoma or ocular hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | SDP-133 | one drop |
| DRUG | Lumigan | one drop |
Timeline
- Start date
- 2019-06-10
- Primary completion
- 2019-07-08
- Completion
- 2019-07-08
- First posted
- 2019-04-25
- Last updated
- 2021-11-19
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03927443. Inclusion in this directory is not an endorsement.