The Safety and Effectiveness of BI-RG-587 in HIV-Infected Patients
NCT ID: NCT00000962
Last Updated: 2008-08-04
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
Recruitment Status
COMPLETED
Clinical Phase
PHASE1
Total Enrollment
30 participants
Study Classification
INTERVENTIONAL
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
To assess the safety and tolerance of multiple oral doses of Nevirapine (BI-RG-587). To generate data on the pharmacokinetics and dose proportionality of Nevirapine with multiple dosing. To characterize the pattern of virological activity in vivo. Improvement in virological end points will be examined for association with dose and absorption. To determine whether development of resistance is reflected in return of virological activity and, if so, when markers reflect this resistance. To determine if improvements of immunological endpoints are detectable in the number of patients studied. A compound free of the toxic effects of nucleoside chain terminators such as zidovudine (AZT) may have an advantage over currently available treatments for HIV infection. Such a compound has further advantages if it is active against AZT-resistant isolates. Nevirapine (BI-RG-587) has shown in vitro inhibitory activity against HIV-1 reverse transcriptase (RT). The molecular mechanism of the RT inhibitory effect is hypothesized to be non-competitive inhibition due to its binding to an RT site distinct from those for the RNA template primer, the deoxynucleotide triphosphate or the RNase H catalytic site.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A compound free of the toxic effects of nucleoside chain terminators such as zidovudine (AZT) may have an advantage over currently available treatments for HIV infection. Such a compound has further advantages if it is active against AZT-resistant isolates. Nevirapine (BI-RG-587) has shown in vitro inhibitory activity against HIV-1 reverse transcriptase (RT). The molecular mechanism of the RT inhibitory effect is hypothesized to be non-competitive inhibition due to its binding to an RT site distinct from those for the RNA template primer, the deoxynucleotide triphosphate or the RNase H catalytic site.
This is a staggered dose escalation cohort trial which examines the safety, tolerance, pharmacokinetics and activity of Nevirapine (BI-RG-587) in patients with HIV infection. Groups of 10 patients must have completed 4 weeks of therapy without requiring dose interruption before the next dosage level can be initiated. All 10 patients must be enrolled at a lower dosage level before the next dosage level can be initiated. Patients discontinue antiretroviral therapy, after signing informed consent, 28 days prior to receipt of a first dose of Nevirapine. Screening lab tests, including p24 antigen and plasma viremia, and CD4+ cell count determination are performed 21 days prior to drug dosing in Part I. Patients are notified of screening laboratory measures that exclude them from study participation. Upon such notification patients have the option to resume prior antiretroviral therapy or to repeat those values in one week. Part II consists of two 8-hour intensive blood sampling periods plus frequent trough value blood samplings. Safety, trough value blood sampling, and activity assessments are performed in Part III. An assessment of dose-tolerance and of activity is made in Study Week 12 in order that patients may continue Nevirapine chronic therapy for an additional 12 weeks. The Final Visit in Part IV takes place on Study Week 24 to complete the trial. Patients who complete 24 weeks are offered the option to continue on Nevirapine chronic therapy at the initial or an altered dose on a separate open-label protocol.
This is a staggered dose escalation cohort trial which examines the safety, tolerance, pharmacokinetics and activity of Nevirapine (BI-RG-587) in patients with HIV infection. Groups of 10 patients must have completed 4 weeks of therapy without requiring dose interruption before the next dosage level can be initiated. All 10 patients must be enrolled at a lower dosage level before the next dosage level can be initiated. Patients discontinue antiretroviral therapy, after signing informed consent, 28 days prior to receipt of a first dose of Nevirapine. Screening lab tests, including p24 antigen and plasma viremia, and CD4+ cell count determination are performed 21 days prior to drug dosing in Part I. Patients are notified of screening laboratory measures that exclude them from study participation. Upon such notification patients have the option to resume prior antiretroviral therapy or to repeat those values in one week. Part II consists of two 8-hour intensive blood sampling periods plus frequent trough value blood samplings. Safety, trough value blood sampling, and activity assessments are performed in Part III. An assessment of dose-tolerance and of activity is made in Study Week 12 in order that patients may continue Nevirapine chronic therapy for an additional 12 weeks. The Final Visit in Part IV takes place on Study Week 24 to complete the trial. Patients who complete 24 weeks are offered the option to continue on Nevirapine chronic therapy at the initial or an altered dose on a separate open-label protocol.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
HIV Infections
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Drug Evaluation
Acquired Immunodeficiency Syndrome
AIDS-Related Complex
Nevirapine
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
Primary Study Purpose
TREATMENT
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Nevirapine
Intervention Type
DRUG
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Concurrent Medication:
Allowed:
* Pentamidine or dapsone prophylaxis for Pneumocystis carinii pneumonia (PCP) in patients with a CD4+ cell count = or \< 200 cells/mm3.
* Antifungal prophylaxis with oral fluconazole or ketoconazole.
* Antiviral prophylaxis with a maximum of 1 gram of oral acyclovir per day.
* Acute therapy for intercurrent infections so long as that therapy is not an excluded medication of an excluded opportunistic infection.
Patients must have:
* Positive HIV antibody test results by ELISA.
* Average of CD4+ cell count at 60 and at 21 days prior to study beginning = or \< 400 cells/mm3.
* Seven of 10 patients in each treatment arm must have p24 antigen levels = or \> 70 pg/ml (\> 50 pg/ml at U. of Mass. site only) or be plasma viremic.
* Preserved hematologic, hepatic, and renal function as defined by required lab values.
* Ambulatory performance score of = or \> 70 Karnofsky.
* Ability to voluntarily provide written informed consent prior to treatment.
* Willingness and ability to follow protocol requirements.
Allowed:
* Pentamidine or dapsone prophylaxis for Pneumocystis carinii pneumonia (PCP) in patients with a CD4+ cell count = or \< 200 cells/mm3.
* Antifungal prophylaxis with oral fluconazole or ketoconazole.
* Antiviral prophylaxis with a maximum of 1 gram of oral acyclovir per day.
* Acute therapy for intercurrent infections so long as that therapy is not an excluded medication of an excluded opportunistic infection.
Patients must have:
* Positive HIV antibody test results by ELISA.
* Average of CD4+ cell count at 60 and at 21 days prior to study beginning = or \< 400 cells/mm3.
* Seven of 10 patients in each treatment arm must have p24 antigen levels = or \> 70 pg/ml (\> 50 pg/ml at U. of Mass. site only) or be plasma viremic.
* Preserved hematologic, hepatic, and renal function as defined by required lab values.
* Ambulatory performance score of = or \> 70 Karnofsky.
* Ability to voluntarily provide written informed consent prior to treatment.
* Willingness and ability to follow protocol requirements.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
* Active cytomegalovirus disease.
* Toxoplasmic encephalitis requiring suppressive therapy.
* Mycobacteriosis requiring maintenance chemotherapy.
* Visceral Kaposi's sarcoma requiring chemotherapy and/or irradiation.
* Malignancy other than Kaposi's sarcoma or limited cutaneous basal cell carcinoma.
* More than mild diarrhea (defined as more than transient or \> 4 loose stools per day).
Concurrent Medication:
The following medications / substances may NOT be ingested up to one hour before or 4 hours after a Nevirapine dose:
* Antacids (particularly those containing calcium carbonate).
* Cimetidine.
* Carafate.
* Cholestyramine resin.
* Alcohol and alcohol-containing substances.
* Benzodiazepines (diazepam, triazolam).
Excluded:
* Any approved or investigational antiretroviral, immunosuppressive, or cytotoxic drugs.
* Glucocorticoids and steroid hormones (including oral contraceptives).
* Dicumarol, warfarin, and other anticoagulant medications.
* Nitroglycerin.
* Digitoxin.
* Valproic acid.
* Tolbutamide.
* Doxycycline.
* Chloramphenicol.
* Isoniazid.
* Any sulfonamide medications.
Patients with the following are excluded:
* History of clinically important disease other than HIV infection defined by the investigator as possibly putting the patient at risk during study participation.
* Conditions listed in Exclusion Co-Existing Conditions and symptoms.
* Having received any approved or investigational antiretroviral, immunosuppressive, or cytotoxic drugs or any other experimental drug with 4 weeks of study entry.
* A positive zidovudine (AZT) detection assay performed 7 days prior to drug dosing will exclude patients from study participation.
Prior Medication:
Excluded within 4 weeks of study entry:
* Any approved or investigational antiretroviral, immunosuppressive or cytotoxic drugs.
* Glucocorticoids and steroid hormones (including oral contraceptives).
* Dicumarol, warfarin, and other anticoagulant drugs.
* Nitroglycerin. Digitoxin.
* Valproic acid.
* Tolbutamide.
* Doxycycline.
* Chloramphenicol.
* Isoniazid.
* Antiepileptics (phenobarbital and other barbiturates).
* Trimethoprim / sulfamethoxazole (Bactrim).
Risk Behavior:
Excluded:
* Patients whose use of alcohol or drugs is sufficient to impair compliance with protocol requirements.
Patients with the following symptoms or conditions are excluded:
* Active cytomegalovirus disease.
* Toxoplasmic encephalitis requiring suppressive therapy.
* Mycobacteriosis requiring maintenance chemotherapy.
* Visceral Kaposi's sarcoma requiring chemotherapy and/or irradiation.
* Malignancy other than Kaposi's sarcoma or limited cutaneous basal cell carcinoma.
* More than mild diarrhea (defined as more than transient or \> 4 loose stools per day).
Concurrent Medication:
The following medications / substances may NOT be ingested up to one hour before or 4 hours after a Nevirapine dose:
* Antacids (particularly those containing calcium carbonate).
* Cimetidine.
* Carafate.
* Cholestyramine resin.
* Alcohol and alcohol-containing substances.
* Benzodiazepines (diazepam, triazolam).
Excluded:
* Any approved or investigational antiretroviral, immunosuppressive, or cytotoxic drugs.
* Glucocorticoids and steroid hormones (including oral contraceptives).
* Dicumarol, warfarin, and other anticoagulant medications.
* Nitroglycerin.
* Digitoxin.
* Valproic acid.
* Tolbutamide.
* Doxycycline.
* Chloramphenicol.
* Isoniazid.
* Any sulfonamide medications.
Patients with the following are excluded:
* History of clinically important disease other than HIV infection defined by the investigator as possibly putting the patient at risk during study participation.
* Conditions listed in Exclusion Co-Existing Conditions and symptoms.
* Having received any approved or investigational antiretroviral, immunosuppressive, or cytotoxic drugs or any other experimental drug with 4 weeks of study entry.
* A positive zidovudine (AZT) detection assay performed 7 days prior to drug dosing will exclude patients from study participation.
Prior Medication:
Excluded within 4 weeks of study entry:
* Any approved or investigational antiretroviral, immunosuppressive or cytotoxic drugs.
* Glucocorticoids and steroid hormones (including oral contraceptives).
* Dicumarol, warfarin, and other anticoagulant drugs.
* Nitroglycerin. Digitoxin.
* Valproic acid.
* Tolbutamide.
* Doxycycline.
* Chloramphenicol.
* Isoniazid.
* Antiepileptics (phenobarbital and other barbiturates).
* Trimethoprim / sulfamethoxazole (Bactrim).
Risk Behavior:
Excluded:
* Patients whose use of alcohol or drugs is sufficient to impair compliance with protocol requirements.
Minimum Eligible Age
18 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Boehringer Ingelheim
INDUSTRY
Sponsor Role
collaborator
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Sponsor Role
lead
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Univ of California / San Diego Treatment Ctr
San Diego, California, United States
Site Status
Univ of Massachusetts Med Ctr
Worcester, Massachusetts, United States
Site Status
Univ of Minnesota
Minneapolis, Minnesota, United States
Site Status
Countries
Review the countries where the study has at least one active or historical site.
United States
References
Explore related publications, articles, or registry entries linked to this study.
Greenough TC. Quantitative virology: the experience during the nevirapine phase I/II trials. ACTG 164/168 Study Team. Int Conf AIDS. 1992 Jul 19-24;8(2):B192 (abstract no PoB 3610)
Reference Type
BACKGROUND
Havlir D, Cheeseman SH, McLaughlin M, Murphy R, Erice A, Spector SA, Greenough TC, Sullivan JL, Hall D, Myers M, et al. High-dose nevirapine: safety, pharmacokinetics, and antiviral effect in patients with human immunodeficiency virus infection. J Infect Dis. 1995 Mar;171(3):537-45. doi: 10.1093/infdis/171.3.537.
Reference Type
BACKGROUND
Havlir D. Antiviral activity of nevirapine at 400 mg in p24 antigen positive adults. ACTG 164 and 168 Study Teams. Int Conf AIDS. 1993 Jun 6-11;9(1):69 (abstract no WS-B26-1)
Reference Type
BACKGROUND
Richman DD. Loss of nevirapine activity associated with the emergence of resistance in clinical trials. The ACTG 164/168 Study Team. Int Conf AIDS. 1992 Jul 19-24;8(2):B183 (abstract no PoB 3576)
Reference Type
BACKGROUND
Hattox S. Pharmacokinetics of nevirapine alone and in combination with zidovudine. The ACTG 164/168 Study Team. Int Conf AIDS. 1992 Jul 19-24;8(2):B185 (abstract no PoB 3591)
Reference Type
BACKGROUND
Cheeseman SH, Murphy RL, Saag MS, Havlir D. Safety of high dose nevirapine (NVP) after 200 mg/d lead-in. ACTG 164/168 Study Team. Int Conf AIDS. 1993 Jun 6-11;9(1):487 (abstract no PO-B26-2109)
Reference Type
BACKGROUND
Cheeseman SH. Nevirapine (NVP) alone and in combination with zidovudine (ZDV): safety and activity. The ACTG 164/168 Study Team. Int Conf AIDS. 1992 Jul 19-24;8(1):Mo15 (abstract no MoB 0053)
Reference Type
BACKGROUND
Zhang H, Dornadula G, Wu Y, Havlir D, Richman DD, Pomerantz RJ. Kinetic analysis of intravirion reverse transcription in the blood plasma of human immunodeficiency virus type 1-infected individuals: direct assessment of resistance to reverse transcriptase inhibitors in vivo. J Virol. 1996 Jan;70(1):628-34. doi: 10.1128/JVI.70.1.628-634.1996.
Reference Type
BACKGROUND
Murphy RL, Montaner J. Nevirapine: A review of its development, pharmacological profile and potential for clinical use. Exp Opin Invest Drugs. 1996;5(9): 1183-1199
Reference Type
BACKGROUND
Cheeseman SH, Havlir D, McLaughlin MM, Greenough TC, Sullivan JL, Hall D, Hattox SE, Spector SA, Stein DS, Myers M, et al. Phase I/II evaluation of nevirapine alone and in combination with zidovudine for infection with human immunodeficiency virus. J Acquir Immune Defic Syndr Hum Retrovirol. 1995 Feb 1;8(2):141-51.
Reference Type
BACKGROUND
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
00744
Identifier Type: -
Identifier Source: secondary_id
ACTG 164
Identifier Type: -
Identifier Source: org_study_id