Trials / Completed
CompletedNCT01417780
Evaluation of Safety, PK and Immunomodulatory Effects of AB103 in Necrotizing Soft Tissue Infections Patients
Evaluation of Safety, Pharmacokinetics and Immunomodulatory Effects of AB103, a CD28 Co-stimulatory Receptor Antagonist, in Patients Diagnosed With Necrotizing Soft Tissue Infections
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 43 (actual)
- Sponsor
- Atox Bio Ltd · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A study to evaluate the safety and pharmacokinetics profile of different doses of AB103 administered to patients diagnosed with Necrotizing Soft Tissue Infections that are scheduled for an urgent surgical intervention as part of their standard of care.
Detailed description
A study to evaluate the safety and pharmacokinetics profile of different doses of AB103 administered to patients diagnosed with Necrotizing Soft Tissue Infections that are scheduled for an urgent surgical intervention as part of their standard of care. The primary study hypothesis is that AB-103 can be administered safely to the patients presenting with Necrotizing Soft Tissue Infections. Secondary endpoints are efficacy by exploratory descriptive analyses of specific efficacy endpoints from three outcome domains to demonstrate treatment benefit of AB103 in comparison to placebo in patients with Necrotizing Soft Tissue Infections. The efficacy domains are: 1. Clinical status domain 2. Pharmacoeconomics domain 3. Systemic and local inflammatory biomarker domain
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AB103 | AB103 0.25 mg/kg or 0.5 mg/kg administered as a single IV infusion |
| DRUG | Placebo | Normal saline (0.9% sodium chloride) administered as a single IV infusion |
Timeline
- Start date
- 2011-12-01
- Primary completion
- 2012-09-01
- Completion
- 2012-09-01
- First posted
- 2011-08-16
- Last updated
- 2021-08-18
- Results posted
- 2021-08-18
Locations
7 sites across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT01417780. Inclusion in this directory is not an endorsement.