Study of the 48-Week Virologic and Immunologic Response to Lopinavir/Ritonavir (Kaletra) in HIV Positive Adult Patients
Information provided by (Responsible Party)
First received: June 29, 2005
Last updated: April 27, 2017
Last Verified: June 2005
History of Changes
Expected Enrollment: 40 patients
Study Start Date: June 2005
- To conduct a pilot study to assess the safety, tolerability, and antiviral activity of Kaletra 400/100 mg taken twice a day (bid) in antiretroviral (ARV)-naïve HIV-infected patients at Week 48
- To determine the proportion of patients with HIV RNA <400 copies/mL at weeks 24 and 48
- To determine the proportion of patients with HIV RNA < 50 at weeks 24 and 48
- To elucidate the specific adverse event (AE) profile of Kaletra single agent therapy
- To assess the proportion of patients below the limit of quantification (LOQ) at each visit. Patients will be observed at baseline, weeks 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44 and 48.
- To determine the time to HIV RNA reaching <400 and <50 copies/mL
- To determine the time to virologic failure
- To assess change from baseline at each visit for HIV RNA and CD4 count at weeks 4, 8, 12, 24 and 48.
- To assess changes in genotype from baseline to time of confirmed virologic failure (2 consecutive HIV RNA measurements >400 copies/mL after suppressing to <400 copies/mL) or at time of treatment intensification.
- To characterize changes in lipid and triglyceride concentrations over time and the effect of treatment with appropriate drugs (fibrate or statin, if necessary) on these elevations.
- To evaluate the safety and tolerability of subjects through 48 weeks of drug exposure.
- To describe virologic response following intensification in Kaletra single agent
Drug : Kaletra
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Official Title:||A Phase II, Open Label, Single Arm Study of the 48-Week Virologic and Immunologic Response to Lopinavir/Ritonavir (Kaletra) as a Single Agent in a Cohort of HIV Positive Adult Patients|
Further study details as provided by Therapeutic Concepts:
Primary Outcome Measures
- Proportion of patients with plasma HIV-1 RNA <400 copies/mL at Week 24 and 48
- Proportion of patients with plasma HIV-1 RNA < 50 copies/mL at Week 48
- Proportion of patients with plasma HIV-1 RNA <400 copies/mL or <50 copies/mL at each study visit
- Proportion of patients with plasma HIV-1 RNA <50 copies/mL at Weeks 24 and 48 Weeks
- Number of weeks until HIV RNA <400 copies/mL and <50 copies/mL, respectively
- Change from baseline to each study visit in plasma HIV-1 RNA and CD4+ cell count
- Time-averaged change from baseline to Weeks 12, 24 and 48 (AUCMB) in plasma HIV-1 RNA and CD4+cell count
- Change in HIV genotype and phenotype in patients who either intensify study therapy or experience virologic rebound
- HIV genomic sequence in treatment failures
- Adverse events and treatment-limiting toxicities at all time points
- Baseline and on-therapy assessment of clinical laboratory parameters
- Change from baseline over time in clinical laboratory parameters including fasted triglycerides, total cholesterol, direct HDL cholesterol and LDL cholesterol
|Study Start Date:||June 2005|
|Study Completion Date:||December 2007|
|Ages Eligible for Study:||18 Years and older|
|Sexes Eligible for Study:||All|
- HIV-1 RNA ≥ 2000 copies/mL by Roche Amplicor 1.5v Primer
- CD4 count -< 400
- CD4 count > 400, with documented understanding of DHHS recommendations related to risks and benefits of early treatment initiation, and stated desire for treatment based upon one of the following conditions: (reference: DHHS guidelines) *Viral load > 100,000 copies; *Symptomatic HIV infection other than an active opportunistic infection - CDC Category B or C condition; *Desire for potential immune function preservation; *Desire for potential decreased risk of HIV transmission to uninfected partner; *Desire for potential prolongation of disease-free survival
- ≥ 18 years of age
- Cognitive ability to understand and provide written informed consent and willingness to participate in and comply with the study protocol
- PI -naïve or has < 7 days of prior ART with any licensed or investigational compound (NOTE: patients must have no prior PI experience)
- Patient does not currently have or has not been treated for an active opportunistic infection (OI) consistent with CDC definition within 30 days of screening
- Vital signs, physical examination and laboratory results do not exhibit evidence of acute illness
- A female is eligible to enter and participate in this study if she is of: (1) Non-childbearing potential (i.e., physiologically incapable of becoming pregnant, including any female who is post-menopausal) -OR- (2) Child-bearing potential, has a negative serum pregnancy test at screen, and agrees to one of the following: Complete abstinence from intercourse from 2 weeks prior to administration of the study drug, throughout the study, and for at least 2 weeks after completion or premature discontinuation from the study to account for elimination of the investigational drug. Should a patient decide to become sexually active during the course of the study, she must be counseled and be willing to use one of the birth control methods listed below: *Double barrier method (male condom/spermicide, male condom/diaphragm, diaphragm/spermicide); *Any intrauterine device (IUD) with published data showing that the expected failure rate is <1% per year (not all IUDs meet this criterion); *Sterilization (female patient or male partner of female patient); *Any other methods with published data showing that the lowest expected failure rate for that method is <1% per year.
NOTE: Data are insufficient to exclude a clinically important interaction of LPV/r with drugs, such as hormonal contraceptives, that are highly metabolized by the cytochrome P450 enzyme system. As a result, hormonal contraception is not considered adequate.
- Patient with active AIDS-defining opportunistic infection or disease according to the 1993 CDC AIDS surveillance definition (Clinical Category C) that, in the opinion of the investigator, would preclude the patient from participating in the study.
- Patient has an M184V mutation in reverse transcriptase, or mutations at 10, 20, 32, 46, 47, 48, 50, 54, 71, 73, 82, 84, or 90;
- K65R mutation or 2 or more TAMs at baseline
- History of active substance abuse, excluding cannabis, or psychiatric illness that, in the opinion of the investigator, would preclude compliance with protocol, dosing schedule and assessments.
- Patient is either pregnant at time of screening evaluation or breast-feeding.
- Patient, in the opinion of the investigator, is unlikely to be able to complete the 48-week dosing period and protocol evaluations and assessments or adhere to the study drug regimen.
- Patient suffers from a serious medical condition, such as diabetes, congestive heart failure, cardiomyopathy or other cardiac dysfunction, which in the opinion of the investigator would compromise the safety of the patient
- Patient has malabsorption syndrome or other gastrointestinal dysfunction, which may interfere with drug absorption or render the patient unable to take oral medication.
- Patient is undergoing interferon therapy for HCV or anticipates undergoing therapy during the course of this trial
- HBV coinfection
- Patient has any of the following laboratory results within 30 days prior to the first dose of study medication: *Hemoglobin concentration < 8.0 g/dL; *Absolute neutrophil count < 750 cells/mm3; *Platelet count <50,000 cells/ mm3; *Aminotransferase (AST, ALT) >3 times ULN; *Serum creatinine >1.5 times the Upper Limits of Normal (ULN)
- Patient has required treatment with radiation therapy or cytotoxic chemotherapeutic agents within 4 weeks prior to entry, or has an anticipated need for these agents within the study period.
- Patient requires treatment with immunomodulating agents, such as systemic corticosteroids, interleukins, or interferon's within 4 weeks prior to study entry, or patients who have received an HIV immunotherapeutic vaccine within 3 months prior to entry. Asthmatic patients using inhaled corticosteroids are eligible for enrollment.
- Patient receiving methadone therapy
- Patients requiring foscarnet therapy or therapy with other agents with documented activity against HIV-1 in vitro.
- Patient prescribed/taking astemizole, terfenadine, cisapride, midazolam, triazolam, flecainide, pimozide, propafenone, St. John's Wort, lovastatin, simvastatin, and rifampin or ergot derivatives
- Patient has a history of allergy to any of the study drugs or any excipients therein.
- In addition, patients non-compliant with study medication during 2 - 4 week study periods despite adherence counseling will not be retained in the study due to increased risk for selective pressure and potential development of protease resistance.
- Patient requires inhaled or intranasal fluticasone.
Contacts and LocationsChoosing to participate in a study is an important personal decision.Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00116636
Locations Show More
|United States, Texas|
|Therapeutic Concepts, P.A.|
|Houston, Texas, United States, 77004|
Sponsors and CollaboratorsTherapeutic Concepts
|Principal Investigator:||Joseph C. Gathe, M.D.||Therapeutic Concepts, P.A.|
|Responsible Party:||Therapeutic Concepts|
|ClinicalTrials.gov Identifier:||NCT00116636 History of Changes|
|Other Study ID Numbers:||70-1002-064|
|Study First Received:||June 29, 2005|
|Last Updated:||April 27, 2017|
Keywords provided by Therapeutic Concepts:HIV
Additional relevant MeSH terms:
ClinicalTrials.gov processed this data on October 17, 2017
This information is provided by ClinicalTrials.gov.