New Era Study: Treatment With Multi Drug Class (MDC) HAART in HIV Infected Patients (NewEra)
This study is ongoing, but not recruiting participants.
Sponsor:
MUC Research GmbH
Collaborators:
Pfizer
Merck
Abbott
Information provided by (Responsible Party):
MUC Research GmbH
ClinicalTrials.gov Identifier:
NCT00908544
First received: May 26, 2009
Last updated: September 22, 2011
Last verified: September 2011
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Purpose
The purpose of this study is to decrease viral reservoirs in N=40 HIV-infected patients with either primary infection or chronic infection and successful HAART for at least three years. All patients will be started on a multi drug HAART including two NRTI, one PI, a CCR5-inhibitor and an integrase inhibitor. Decay of viral reservoirs like latently HIV-infected CD4+ T-cells will be monitored over time.
| Condition | Intervention |
|---|---|
|
HIV Infections |
Drug: 2 NRTI + 1 PI/r + Maraviroc + Raltegravir |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | NEW ERA STUDY - HIV and Eradication: A Multicenter, Open-label, Non-randomized Trial to Evaluate Treatment With Multi-drug Class (MDC) HAART and Its Impact on the Decay Rate of Latently Infected CD4+ T Cells |
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 MUC Research GmbH:
Primary Outcome Measures:
- Cell-associated proviral DNA: infectious units per 10exp6 PBMC (peripheral blood mononuclear cells) and per 10exp6 CD4 cells [ Time Frame: Screening, pre-baseline (only for CHI-patients), baseline, months 1, 3, 6 and then every 6 months until month 84, plus 3 post-follow-up visits ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Plasma HIV RNA (using standard and single copy assays) [ Time Frame: Screening, pre-baseline (only for CHI-patients), baseline, months 1, 3, 6 and then every 6 months until month 84, plus 3 post-follow-up visits ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 40 |
| Study Start Date: | May 2009 |
| Estimated Study Completion Date: | November 2019 |
| Estimated Primary Completion Date: | November 2018 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: PHI-patients
Patients with primary HIV infection (PHI) (see also "Eligibility")
|
Drug: 2 NRTI + 1 PI/r + Maraviroc + Raltegravir
Treatment initiation with multi drug class (MDC) HAART.
Other Names:
|
|
Experimental: CHI-patients
Patients with chronic HIV infection (CHI) and with suppressed plasma viral load for at least three years under continuous HAART (see also "Eligibility")
|
Drug: 2 NRTI + 1 PI/r + Maraviroc + Raltegravir
Treatment intensification of PI-based HAART with Maraviroc and Raltegravir.
Other Names:
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
For all patients:
- HIV-infected patient
- Age greater 18 years
- No acute AIDS-defining disease or history of AIDS- defining disease
- CD4-cell nadir above or equal 200 cells/microliter
- Hemoglobin greater 8 g/dl
- Neutrophil count greater 750 cells/microliter
- Platelet count greater 50.000 cells/microliter
- AST/ALT below 5x upper limit of normal range
- No evidence for drug intolerability
- No prior use of an HIV integrase inhibitor or CCR5 antagonist
- No presence of malignancy (requiring active treatment and malignancy within 5 years prior to enrolment (even if in complete remission)
- No significant underlying disease (non-HIV) that might impinge upon disease progression or death
- No history of alcohol or other substance abuse or other condition which in the opinion of the investigator would interfere with the patient compliance or safety.
- Written informed consent
- For males and premenopausal females use of acceptable methods of birth control during the entire study and for 6 weeks thereafter
- No pregnancy (for premenopausal women: negative serum or urine pregnancy test within 48 hours prior to initiating study medications)
- No breastfeeding
For chronically HIV-infected patients:
- Continuous plasma viral load below 50 copies/ml for the preceding 36 months under HAART (two or less single viral load blips up to 500 copies/ml are allowed)
- Stable HAART (for at least 3 months) prior to the Screening visit consisting of 2 NRTI + 1 PI
- No history of virological failure
- No documented resistance to PI and NRTI
- CCR5-tropic virus
For patients with primary HIV infection:
- Detectable plasma viral load
- ELISA positive or negative and Western Blot negative or positive with less or equal 2 bands at screening visit
- No primary resistance to PI´s and NRTI´s
- CCR5-tropic virus
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00908544
Locations
| Germany | |
| Onkology Karlsruhe | |
| Karlsruhe, Baden-Wuerttemberg, Germany, 76135 | |
| Private Practice for Internal Medicine, Hematology and Oncology | |
| Mannheim, Baden-Wuerttemberg, Germany, 68161 | |
| Private Practice Drs Ulmer/Frietsch/Mueller | |
| Stuttgart, Baden-Wuerttemberg, Germany, 70197 | |
| Practice Dr. med. Lothar Schneider | |
| Fürth, Bavaria, Germany, 90762 | |
| MUC Research | |
| Munich, Bavaria, Germany, 80335 | |
| University Munich University Hospital, Dept. of Infectious Diseases | |
| Munich, Bavaria, Germany, 80336 | |
| Private Practice Drs Pauli/Becker | |
| Munich, Bavaria, Germany, 80331 | |
| ICH Study Center | |
| Hamburg, Germany, 20354 | |
Sponsors and Collaborators
MUC Research GmbH
Pfizer
Merck
Abbott
Investigators
| Study Chair: | Hans Jaeger, MD | MUC Research GmbH |
| Study Chair: | Johannes Bogner, Prof., MD | University Munich, University Hospital, Dept. of Infectious Diseases, |
More Information
No publications provided
| Responsible Party: | MUC Research GmbH |
| ClinicalTrials.gov Identifier: | NCT00908544 History of Changes |
| Other Study ID Numbers: | MUC_NewEra_3.1, 2008-002070-35, 4034932, 08101, ID 8879, IISP #35576 |
| Study First Received: | May 26, 2009 |
| Last Updated: | September 22, 2011 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
Keywords provided by MUC Research GmbH:
|
HIV-infection Primary HIV-infection Proviral DNA Eradication Multi drug class HAART |
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 23, 2013