Kaletra-isentress Treatment Evaluation (KITE)
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Purpose
This study will examine the effectiveness and safety of raltegravir (isentress) when used together with lopinavir/ritonavir (kaletra) for the treatment of HIV-infection. Isentress is a recently, Food and Drug Administration (FDA) approved, HIV medication that has strong effects against the HIV virus. Isentress has been shown in other studies to be safe and well tolerated by HIV patients. Combining this drug with kaletra might enable us to construct a HIV regimen that does not include the more toxic drugs of the nucleoside reverse transcriptase inhibitor class.
Eligible volunteers will undergo the following as part of the study procedure:
- Sign the study consent form and the HIPAA Authorization Form.
- Two-third of subjects, the intervention group (selected by random chance) will have their HIV drug treatment changed to kaletra + isentress.
- The other one-third will continue their usual HIV medications (this will be the control group).
- Make 9 study related visits to the Ponce clinic during the 48 weeks study period. During these visits, medical information will be collected, and blood tests will be performed.
- Perform Dexa-scan on two separate occasions at Emory University Hospital Radiology.
Information collected will be used to assess the effectiveness of this treatment in keeping the HIV virus suppressed, how well these two drugs together is tolerated by HIV-infected patients, and the blood levels of these two drugs when given together.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Kaletra + Isentress |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Pilot Study to Assess the Safety, Efficacy, and PK Profile of a Switch in Antiretroviral Therapy to a RTI Sparing Combination of LPV/r and RAL in Virologically Suppressed HIV-infected Patients |
- To assess the durability of virologic suppression (proportion of patients with plasma HIV-1 RNA PCR <50 copies/ml) with LPV/r + RAL from baseline through week 48 as compared to standard HAART regimen. [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
- To assess the tolerability of combination therapy with LPV/r + RAL (as defined by the Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events toxicity grading scale for symptoms and laboratory abnormalities) [ Time Frame: 48 weeks ] [ Designated as safety issue: Yes ]
| Enrollment: | 60 |
| Study Start Date: | June 2008 |
| Study Completion Date: | January 2011 |
| Primary Completion Date: | January 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Kaletra + Isentress
Kaletra + Isentress
|
Drug: Kaletra + Isentress
Kaletra 400/100 mg + Isentress 400 mg BID
Other Names:
|
|
Active Comparator: Standard HAART
Pre-study standard HAART regimen
|
Drug: Kaletra + Isentress
Kaletra 400/100 mg + Isentress 400 mg BID
Other Names:
|
Detailed Description:
RATIONALE: Virologic failure and adverse effects associated with current highly active antiretroviral therapy (HAART) warrant continuing search for novel combination therapeutic options. Raltegravir's (RAL) was recently shown to be a potent antiretroviral (ARV) agent with a favorable safety profile. If future reports continue to show positive data on this first-in-class integrase inhibitor, there may be a paradigm shift in the currently recommended first line HAART to regimens that will include integrase inhibitors.
Combining RAL with a drug that has a high genetic barrier to resistance, such as lopinavir/ritonavir (LPV/r) may offer a number of advantages. Both agents are potent and should produce durable virologic suppression. Because their combination is reverse transcriptase inhibitor (RTI) class sparing, its tolerability might be superior. In addition, RAL is not metabolized by the cytochrome P-450 enzymes, therefore, a compatible pharmacokinetic profile is expected with this combination. Pairing LPV/r with RAL in early ARV regimens as is proposed in this application may provide a HAART regimen that is highly efficacious and durable, with less resistance and adverse drug events.
DESIGN: This is single center, open label, randomized, controlled, study designed to assess the tolerability, pharmacokinetic compatibility, and the durability of virologic suppression of the RTI sparing combination therapy of LPV/r + RAL. HIV-infected subjects who are virologically suppressed (HIV-RNA PCR < 50 copies/ml) on current HAART regimen will be randomized in a 2:1 fashion to be switched to a regimen consisting of LPV/r + RAL, intervention arm A (n=40), or to be continued on their pre-study HAART regimen, control arm B (n=20). The primary endpoint will be proportion of subjects with sustained virologic suppression (HIV-1 RNA PCR < 50 copies/ml) through week 48. The immunoreconstitution, toxicity profile, and pharmacokinetic profile of the RAL and LPV/r in this novel combination therapy will be evaluated.
DURATION: 48 weeks after the enrollment of the last participant. Enrollment is expected to take about 10 months.
SAMPLE SIZE: 60 subjects.
POPULATION: HIV-infected individuals (male and female), Age > 18 years, who are virologically suppressed (HIV-RNA PCR < 50 copies/ml) on their current HAART regimen for > 6 months.
REGIMEN: For Arm A= LPV/r 400/100 mg (2 tablets) BID + RAL 400 mg (1 tablet) BID taken by mouth. For Arm B=Pre-study HAART regimen.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HIV-1-infected individuals receiving HAART regimen (if on PI-based regimen, must be 1st PI-containing HAART).
- They must have been on and tolerating current HAART regimen for > 6-months.
- Plasma HIV-1 viral load < 50 copies/ml at study entry.
- Men and women age > 18 years (sex is defined as sex at birth).
Laboratory values obtained within 30 days prior to study entry:
- Hemoglobin > 9.4 g/dl
- Creatinine < 2 mg/dl
- AST (SGOT) < 2 x ULN
- ALT (SGPT) < 2 x ULN
- Ability and willingness of subject or legal guardian/representative to give written informed consent.
- No CD4 T-cell counts requirement
Exclusion Criteria:
- Subjects with a history of previous intolerance to or virological failure to LPV/r
- Concomitant drugs (including alternative therapies) that may affect PI or RAL plasma concentrations (inducers or inhibitors of the CYP 3A4 or UDP-glucuronosyltransferase iso-enzymes).
- A known history of noncompliance with medications or a known history of noncompliance with scheduled physician and clinic visits.
- Investigational ARV drug.
- Pregnancy/Breast feeding.
- HBV-coinfected patients receiving nucleoside analogue for both HIV and HBV suppression.
- Active drug or alcohol use or dependence which, in the Investigator's opinion, may interfere with adherence to study requirements or endanger subject's health while on the study.
- Serious illness requiring systemic treatment and/or hospitalization within 30 days prior to the screening visit.
Contacts and Locations| United States, Georgia | |
| Grady Infectious Diseases Program (Ponce Clinic) | |
| Atlanta, Georgia, United States, 30308 | |
| Principal Investigator: | Igho Ofotokun, MD, MSc | Emory University |
More Information
No publications provided
| Responsible Party: | Ighovwerha Ofotokun, Associate Professor of Medicine, Emory University |
| ClinicalTrials.gov Identifier: | NCT00700115 History of Changes |
| Other Study ID Numbers: | KITE-6876 |
| Study First Received: | June 16, 2008 |
| Last Updated: | March 16, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Emory University:
|
HAART lopinavir/ritonavir raltegravir HIV/AIDS patients on HAART Treatment Experienced |
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 Ritonavir |
Lopinavir HIV Protease Inhibitors Protease Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Anti-HIV Agents Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 22, 2013