Trials / Completed
CompletedNCT02191540
Efficacy and Safety Study of Abnoba Viscum F 20mg in Malignant Pleural Effusion Patients
A Phase 3, Multi-Center, Single-Arm, Open-Label Study For The Safety And Efficacy Of Mistletoe Extract (AbnobaViscum® Injection) In Malignant Pleural Effusions
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 68 (actual)
- Sponsor
- Abnoba Korea · Industry
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Phase 3, non-randomized, Multicenter, single arm study to assess efficacy and safety of Abnoba viscum F 20mg in patients with malignant pleural effusion
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Abnoba Viscum F 20mg | intravesical instillation of five amples of AbnobaViscum® F20mg and 0.9% normal saline into the pleural space |
Timeline
- Start date
- 2011-01-01
- Primary completion
- 2013-01-01
- Completion
- 2013-05-01
- First posted
- 2014-07-16
- Last updated
- 2014-07-23
Locations
3 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02191540. Inclusion in this directory is not an endorsement.