Trials / Terminated
TerminatedNCT03148756
Efficacy and Safety of Dalbavancin Compared to Standard of Care Antibiotic Therapy for the Completion of Treatment of Patients With Complicated Bacteremia or Infective Endocarditis
Phase 2, Open-Label, Randomized, Multicenter Study to Compare the Efficacy and Safety of Dalbavancin to Standard of Care Antibiotic Therapy for the Completion of Treatment of Patients With Complicated Bacteremia or Documented Infective Endocarditis
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- AbbVie · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare dalbavancin to standard of care (SOC) antibiotic therapy for the completion of therapy in patients with complicated bacteremia or infective endocarditis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dalbavancin | Dalbavancin 1500 mg, intravenous (IV) administration over 30 minutes on Day 1, and on Day 8. |
| DRUG | Standard of Care | Antibiotic consistent with Standard of Care (SOC), based on baseline pathogen, for 4 to 6 weeks. |
Timeline
- Start date
- 2017-05-12
- Primary completion
- 2017-08-04
- Completion
- 2017-08-04
- First posted
- 2017-05-11
- Last updated
- 2022-04-25
- Results posted
- 2018-09-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03148756. Inclusion in this directory is not an endorsement.