Trials / Completed
CompletedNCT01031966
A Pilot Study to Evaluate ZADAXIN's® (Thymalfasin) Ability to Enhance Immune Response to the H1N1sw Influenza Vaccine
A Pilot, Randomized, Open-label Study in Patients on Chronic Dialysis With End Stage Renal Disease (Esrd), to Evaluate the Enhancing Effect of Two Doses of Thymosin Alpha 1 on the Immunogenicity of h1n1sw Monovalent Vaccine
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- sigma-tau i.f.r. S.p.A. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this explorative trial is to collect preliminary data on efficacy and safety of thymosin alpha 1 given at different doses as an adjuvant to egg-derived H1N1sw monovalent influenza vaccine in hemodialysis patients. The final aim is that of gathering information needed for planning a following confirmatory study on the efficacy and safety of Thymosin alpha 1 in the same indication.
Detailed description
The emergence and spread of the novel influenza A (H1N1) virus has been of great concern globally. Uremic patients are especially vulnerable to infections and it is generally recommended to vaccinate patients with chronic renal insufficiency yearly against influenza. In patients on haemodialysis (HD) the vaccination response has been considered suboptimal. Decreased antibody response to T-cell dependent antigens may be one factor that accounts for insufficient efficacy of certain vaccination programs (eg, influenza). Diminished antibody responses have also been reported in patients with end-stage renal disease. The evidence for impairment of cell-mediated immunity in hemodialysis patients has been attributed to incompetence in T-cell-mediated immune responses. Since Zadaxin can enhance T-cell-dependent specific antibody production, the addition of Zadaxin (Thymosin alpha 1)to vaccination programs for immunocompromised individuals should be effective.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | MF59 adjuvanted H1N1 influenza monovalent vaccine | One/two single administration |
| DRUG | Thymosin alpha 1 | 1.6 mg, 3.2 mg seven days before vaccination (study day -7) and at the same day of vaccination (study day 0) |
| DRUG | Thymosin alpha 1 | 1.6 mg, 6.4 mg seven days before vaccination (study day -7) and at the same day of vaccination (study day 0) |
Timeline
- Start date
- 2009-11-01
- Primary completion
- 2010-05-01
- Completion
- 2010-07-01
- First posted
- 2009-12-15
- Last updated
- 2012-03-29
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT01031966. Inclusion in this directory is not an endorsement.