Drug Levels of Tablet and Liquid Forms of Lamivudine, Nevirapine, and Stavudine in HIV Infected Thai Children

HIV Infections Clinical Trial

Official title:

A Phase I/II Comparative Pharmacokinetic Study of the Fixed-Dose Combination (FDC) of Stavudine (d4T), Lamivudine (3TC), and Nevirapine (NVP) as GPO-VIR Pediatric Chewable Tablets Versus the Individual Liquid Formulations in HIV Infected Children 6 Months and Older to Less Than 13 Years of Age in Thailand

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00312091
• Other study ID #: P1056
• Secondary ID: 10139PACTG P1056
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: December 2006
• Est. completion date: September 2008

Study information

• Verified date: October 2021
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare the blood levels, absorption, and breakdown of lamivudine (3TC), nevirapine (NVP), and stavudine (d4T) in a fixed-dose tablet to that of the individual liquid formulations of the same anti-HIV drugs in HIV infected Thai children.

Description:

The Thai Ministry of Public Health strives to provide the HIV infected people of Thailand with affordable antiretrovirals (ARVs). A fixed-dose combination tablet of 3TC, NVP, and d4T is recommended as first-line treatment in HIV infected adults in Thailand. There has been no similar product developed for children for several reasons: pediatric dosing is based on age, weight, or body surface area; developmental changes may influence the bioavailability and pharmacokinetics (PK) of ARVs; and medication adherence may also be a problem. The purpose of this study is to gather bioavailability and PK data in children taking a fixed-dose tablet of 3TC, NVP, and d4T. This information will then be compared to the bioavailability and PK of the individual liquid formulations of these ARVs.

This study has two stages. Stage 1 will last a minimum of 4 weeks; Stage 2 will last a minimum of 8 weeks. In Stage 1, patients will be randomly assigned to one of two arms. Arm A will receive the fixed-dose tablet twice daily for 2 weeks, then switch to the individual liquid formulations twice daily for 2 weeks. Arm B will receive the individual liquid formulations twice daily for 2 weeks, then switch to the fixed-dose tablet twice daily for 2 weeks. To encourage medication adherence, study staff will make home visits and phone calls to each patient's parent or guardian the first week of each treatment regimen. Medical history, a physical exam, and urine collection will occur on Days 11 and 25. Also on Days 11 and 25, patients will be admitted to the hospital to ensure 100% medication adherence and to provide blood for PK studies.

Stage 1 patients are not eligible for Stage 2. In Stage 2, patients will be stratified by body weight, then randomly assigned to one of two arms. Arm A will receive the fixed-dose tablet twice daily for 4 weeks, then switch to the individual liquid formulations twice daily for 4 weeks. Arm B will receive the individual liquid formulations twice daily for 4 weeks, then switch to the fixed-dose tablet twice daily for 4 weeks. To encourage medication adherence, study staff will make home visits and phone calls to each patient's parent or guardian the first week of each treatment regimen. Medical history, documentation of direct observation of therapy (DOT), a physical exam, and urine collection will occur on Days 25 and

53. Also on Days 25 and 53, patients will be admitted to the hospital to ensure 100% medication adherence and to provide blood for PK studies.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: September 2008
• Est. primary completion date: September 2008
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Months to 13 Years

Eligibility

Inclusion Criteria for Stages 1 and 2:

• HIV infected

• On a highly active antiretroviral regimen (HAART) including NVP and 2 nucleoside reverse transcriptase inhibitors and receiving a maintenance of NVP for at least 4 weeks prior to study entry and taking the current recommended oral dose every 12 hours

• Willing to swallow or chew study drugs

• Willing to be hospitalized for the 12 hour PK studies

• Willing to use acceptable forms of contraception

• Parent or guardian willing to provide informed consent

Inclusion Criteria for Stage 1:

• Between 12 to 30 kg (26.5 to 66.1 lbs)

Inclusion Criteria for Stage 2:

• Between 6 to 30 kg (13.2 to 66.1 lbs)

Exclusion Criteria:

• Certain abnormal laboratory values

• Require certain medications

• Grade 2 or greater vomiting within 30 days prior to study entry

• Grade 2 or greater diarrhea within 30 days prior to study entry

• History of immunological failure (CD4 percentage decrease of more than 30% within a 6-month period for children 6 years or younger OR CD4 cell count decrease of more than 30% within a 6-month period for children older than 6 years)

• Current treatment for acute serious bacterial, viral, or opportunistic infection

• History of dose-limiting toxicity requiring treatment discontinuation of any of the study drugs

• Known hypersensitivity to any of the study drugs

• Current surgical or medical problem affecting gastrointestinal motility or absorption (e.g., ileus, ulcerative colitis) or liver function

• Treatment with immune modulators or myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic, or cytotoxic drugs within 30 days prior to study entry. Patients who have received therapeutic vaccines are not excluded.

• Treatment with experimental drugs within 30 days of study entry

• Acute inflammation of the liver

• Chemotherapy for active cancer

• Any clinically significant diseases other than HIV infection or clinically significant findings that, in the investigator's opinion, may interfere with the study

• Inability to provide a reliable means of contact (e.g., telephone number)

• Pregnancy

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Lamivudine, nevirapine, and stavudine fixed-dose tablet
7 mg d4T, 30 mg 3TC, 50 mg NVP tablet
• Lamivudine
Dosage dependent on weight. More information on this criterion can be found in the protocol.
• Nevirapine
Dosage dependent on weight. More information on this criterion can be found in the protocol.
• Stavudine
Dosage dependent on weight. More information on this criterion can be found in the protocol.

Locations

Country	Name	City	State
Thailand	Queen Sirikit National Institute of Child Health, Pediatric Infectious Unit	Bangkok	Ratchathewi
Thailand	Siriraj Hospital Mahidol University CRS	Bangkok	Ratchathewi
Thailand	Chiang Mai University Pediatrics-Obstetrics CRS	Chiang Mai
Thailand	Chonburi Hosp. CRS	Chonburri

Sponsors (3)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), International Maternal Pediatric Adolescent AIDS Clinical Trials Group

Country where clinical trial is conducted

Thailand, 

References & Publications (4)

Chokephaibulkit K, Plipat N, Cressey TR, Frederix K, Phongsamart W, Capparelli E, Kolladarungkri T, Vanprapar N. Pharmacokinetics of nevirapine in HIV-infected children receiving an adult fixed-dose combination of stavudine, lamivudine and nevirapine. AIDS. 2005 Sep 23;19(14):1495-9. — View Citation

Hoody DW, Fletcher CV. Pharmacology considerations for antiretroviral therapy in human immunodeficiency virus (HIV)-infected children. Semin Pediatr Infect Dis. 2003 Oct;14(4):286-94. Review. — View Citation

King JR, Kimberlin DW, Aldrovandi GM, Acosta EP. Antiretroviral pharmacokinetics in the paediatric population: a review. Clin Pharmacokinet. 2002;41(14):1115-33. Review. — View Citation

Vanprapar N, Cressey TR, Chokephaibulkit K, Muresan P, Plipat N, Sirisanthana V, Prasitsuebsai W, Hongsiriwan S, Chotpitayasunondh T, Eksaengsri A, Toye M, Smith ME, McIntosh K, Capparelli E, Yogev R; IMPAACT P1056 Team. A chewable pediatric fixed-dose co — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparative bioavailability		Throughout study
Primary	therapeutic adequacy		Throughout study
Secondary	Drug absorption from standard pharmacokinetic (PK) analyses		Throughout study

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