Study of the Effectiveness of Passive Immunotherapy in HIV-Infected Patients Who Are in Virologic Failure
This study has suspended participant recruitment.
(low recruitment)
Sponsor:
Hospital Clinic of Barcelona
Information provided by:
Hospital Clinic of Barcelona
ClinicalTrials.gov Identifier:
NCT00353327
First received: July 17, 2006
Last updated: March 28, 2008
Last verified: March 2008
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Purpose
To study the effect of passive immunotherapy (PIT) over the HIV-viral load and the CD4 T+-cell counts in patients who have failed to respond to three different Highly-Active Antiretroviral Therapy (HAART), and who have at the moment less than 100 CD4+-T cells/ml and a viral load over 20,000 copies/ml.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infection |
Procedure: Plasma infusion |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Passive Immunotherapy in HIV-Infected Patients Who Fail to Respond to Multiple Highly Active Antiretroviral Treatment. Randomized Study in Two Phases. |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by Hospital Clinic of Barcelona:
Primary Outcome Measures:
- Lowering of plasma viral load after the first plasma infusion
- Lowering of plasma viral load after a year
Secondary Outcome Measures:
- Elevation of CD4 T cell count
- Negativation of p24 HIV antigen
- HIV RNA mutations conferring resistance to HAART
- Development of C-events
- Dead
- Toxicity
- Accomplishment
| Estimated Enrollment: | 30 |
| Study Start Date: | October 2006 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- HIV-1 infected patients (CDC C category) confirmed by a Western-blot
- CD4 T cell count under 100/ml form 6 months before the inclusion, and who have never been over 600 CD4 T cells/ml in the last 6 months, even if they have been receiving HAART.
- The patients have received at least 3 different HAART regimens, and they have failed to respond (define failure: CD4 T cell count under 100/ml and plasma viral load over 20,000 copies/ml).
- Plasma viral load over 20,000 copies/ml during at least 6 months.
- Written informed consent
- 18 years old or older
Exclusion Criteria:
- Asymptomatic patients who fill the A category of the CDC (1993)
- Younger than 18 years old
- Who are not expected to accomplish the treatment or the follow up visits
- Pregnancy, breast-feeding women, or women who want to get pregnant
- Denied consent
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Felipe García, Hospital Clinic |
| ClinicalTrials.gov Identifier: | NCT00353327 History of Changes |
| Other Study ID Numbers: | PIT-01 |
| Study First Received: | July 17, 2006 |
| Last Updated: | March 28, 2008 |
| Health Authority: | Spain: Ministry of Health |
Keywords provided by Hospital Clinic of Barcelona:
|
HIV Passive immunotherapy |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on May 21, 2013