Therapeutic Intensification Plus Immunomodulation to Decrease the HIV-1 Viral Reservoir (EraMune02)
This study is ongoing, but not recruiting participants.
Sponsor:
Robert L. Murphy
Collaborators:
Objectif Recherche Vaccins SIDA
Pfizer
Merck
Information provided by (Responsible Party):
Robert L. Murphy, Northwestern University
ClinicalTrials.gov Identifier:
NCT00976404
First received: September 9, 2009
Last updated: June 29, 2012
Last verified: June 2012
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The objective of this study is to discover a new approach in which human immunodeficiency virus (HIV) can be eradicated from an infected individual by intensified antiretroviral treatment coupled with immunomodulation. The hypothesis is that eradication is possible only if very potent antiretroviral drugs are delivered in conjunction with an immunomodulatory agent that simultaneously attack the viral reservoirs.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections Treatment Experienced |
Biological: DNA + HIV-rAd5 vaccine Drug: ART intensification (raltegravir) Drug: ART intensification (maraviroc) |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Multicenter, Randomized, Non-comparative, Controlled Study of Therapeutic Intensification Plus Immunomodulation in HIV-infected Patients With Long-term Viral Suppression |
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 Northwestern University:
Primary Outcome Measures:
- HIV proviral DNA [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- HIV DNA in gut lymphoid tissue [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- HIV plasma viral load (RNA) [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- CD4+ T cell count [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- HIV-specific immunity [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- T cell activation (CD38) [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- Adenovirus-specific immunity [ Time Frame: 56 weeks ] [ Designated as safety issue: No ]
- Adverse events attributed to study treatments (raltegravir, maraviroc, or HIV-recombinant Ad5-based vaccine) [ Time Frame: 56 weeks ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 28 |
| Study Start Date: | November 2009 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: ART intensification only
Maintenance of suppressive ART with the addition of raltegravir and maraviroc.
|
Drug: ART intensification (raltegravir)
raltegravir 400 mg PO BID for 56 weeks
Other Name: Isentress
Drug: ART intensification (maraviroc)
maraviroc 150, 300, or 600 mg PO BID (depending on PK interactions with other medications) for 56 weeks
Other Names:
|
|
Experimental: ART intensification plus immunomodulation
Maintenance of suppressive ART with the addition of raltegravir and maraviroc PLUS immunomodulation therapy with HIV-recombinant Ad5-based vaccine (added after 8 weeks of ART intensification)
|
Biological: DNA + HIV-rAd5 vaccine
4 mg subcutaneous injection at weeks 8 (DNA prime), 12 (DNA prime), 16 (DNA prime), and 32 (HIV-rAd5)
Drug: ART intensification (raltegravir)
raltegravir 400 mg PO BID for 56 weeks
Other Name: Isentress
Drug: ART intensification (maraviroc)
maraviroc 150, 300, or 600 mg PO BID (depending on PK interactions with other medications) for 56 weeks
Other Names:
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- HIV-1 infection
- At least 3 years of ART without interruption (less than one month cumulative)
- ART regimen unchanged in the 3 months prior to screening
- One HIV plasma viral load (RNA) documented at least 3 years prior to entry, and at least 2 HIV plasma viral load (RNA) documented per year thereafter
- HIV plasma viral load (RNA) ≤ 500 copies/mL at least 3 years prior to entry, and HIV plasma viral load < 500 copies/mL for >90% of the measures thereafter
- HIV plasma viral load (RNA) below the limit of detection for all values within the past year (one virologic blip allowed)
- HIV plasma viral load below the limit of detection within 60 days of entry
- CD4+ count ≥ 350 cells/mm3 within 60 days of entry
- Proviral DNA ≥10 and ≤1000 copies/106 PBMCs within 75 days of entry
- Adeno5 neutralizing antibody titers of 250 or less within 75 days of entry
- Hemoglobin ≥ 10 g/dL within 60 days of entry
- Platelets ≥ 100,000 per microliter within 60 days of entry
- Hepatic transaminases (ALT and AST) ≤ 2.5 x ULN within 60 days of entry
- Creatinine clearance > 50 mL/min by the Cockcroft-Gault equation within 60 days of entry
Exclusion Criteria:
- Sexually active men and women who will not practice at least one form of barrier birth control (male partner using condoms, female partner using condoms, other barrier contraception, etc)
- Pregnancy
- Inability or unwillingness to provide informed consent
- HBsAg positive
- HCV antibody positive or HCV RNA detectable
- Previous use of an integrase inhibitor (ie raltegravir) or a CCR5 inhibitor (ie maraviroc, vicriviroc). Use of raltegravir for non-treatment failure indications such as intensification or toxicity switches is allowed.
- Immunologic therapeutic intervention (e.g. IL-2) within the past year
- Participation in another clinical drug or device trial where the last dose of drug was within the past 30 days or an investigational medical device is currently implanted
- Diagnosis of cancer within the last 5 years (except basal cell cutaneous cancers and cutaneous KS not requiring systemic therapy)
- Co-morbid condition with an expected survival of less than 12 months
- History of hypersensitivity to vaccination
- History of autoimmune disease, such as systemic lupus erythematosis (SLE) or Hashimoto's thyroiditis
- Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00976404
Locations
| United States, California | |
| University of California San Francisco | |
| San Francisco, California, United States, 94110 | |
| United States, Illinois | |
| Northwestern University | |
| Chicago, Illinois, United States, 60611 | |
| United States, New York | |
| Cornell University | |
| New York, New York, United States, 10011 | |
Sponsors and Collaborators
Robert L. Murphy
Objectif Recherche Vaccins SIDA
Pfizer
Merck
Investigators
| Study Chair: | Robert Murphy, MD | Northwestern University |
More Information
No publications provided
| Responsible Party: | Robert L. Murphy, Professor, Northwestern University |
| ClinicalTrials.gov Identifier: | NCT00976404 History of Changes |
| Other Study ID Numbers: | EraMune02 |
| Study First Received: | September 9, 2009 |
| Last Updated: | June 29, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Northwestern University:
|
HIV-1 infection |
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 June 17, 2013