Trials / Terminated
TerminatedNCT00347646
A Study to Evaluate Plasmin for the Creation of a Posterior Vitreous Detachment (PVD)
An Open Label Sequential Dose Response Observational Study of Intravitreally Administered Plasmin for the Creation of a Posterior Vitreous Detachment (PVD)
- Status
- Terminated
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 4 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Plasmin is expected to create a posterior vitreous detachment (PVD) when injected directly into the eye. The pharmacological creation of a PVD may be beneficial in helping to treat a variety of conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Plasmin | 27 mg of human-derived plasmin to be reconstituted with of 0.9% Sterile Sodium Chloride for a single intravitreal injection |
Timeline
- Start date
- 2006-09-01
- Primary completion
- 2007-05-01
- Completion
- 2007-06-01
- First posted
- 2006-07-04
- Last updated
- 2019-06-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00347646. Inclusion in this directory is not an endorsement.