Completed

Safety, Tolerability, and Plasma Concentration of L-735,524 Capsules in HIV-Positive Children and Adolescents

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What is being tested

Indinavir sulfate

Drug
Who is being recruted

Blood-Borne Infections+14

+ Urogenital Diseases

+ Genital Diseases

From 10 to 18 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 1
Interventional
See protocol details

Summary

Principal SponsorMerck Sharp & Dohme LLC
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Patients receive MK-639 for 14 and one-third days. Repeat plasma samples are collected up to 8 hours following the first and last dose. Urine samples are collected on days 1 and 5.

Principal SponsorMerck Sharp & Dohme LLC
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

12 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 10 to 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood-Borne InfectionsUrogenital DiseasesGenital DiseasesCommunicable DiseasesImmunologic Deficiency SyndromesImmune System DiseasesInfectionsRetroviridae InfectionsRNA Virus InfectionsSexually Transmitted DiseasesSlow Virus DiseasesVirus DiseasesSexually Transmitted Diseases, ViralLentivirus InfectionsAcquired Immunodeficiency SyndromeAIDS-Related ComplexHIV Infections

Criteria

Inclusion Criteria Patients must have: HIV positivity. No active opportunistic infection within the past 30 days, other than superficial candidiasis of the oral cavity or vagina. Body surface area at least 1.0 sqm. Consent of parent or guardian. Prior Medication: Allowed: Aerosolized pentamidine. Topical antifungals. TMP / SMX. AZT. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Significant hepatic disease including HBsAg or hepatitis C positivity. Significant neurologic disease such as loss of intellectual ability, motor deficits, or seizure disorder. Significant cardiac disease including dysrhythmia or cardiomyopathy. Significant medical condition or laboratory abnormality that may pose additional risk to patient on study or confound the results. Has a social situation that may interfere with study participation. Concurrent Medication: Excluded: Oral contraceptives. Patients with the following prior conditions are excluded: History of serious allergic drug reactions. History of significant cardiac disease. Participation on another clinical trial within the past 4 weeks. Donated blood within the past 4 weeks. Prior Medication: Excluded within the past 4 weeks: Hematopoietic growth factors. Excluded within the past 2 weeks: Antiretroviral agent other than zidovudine. Oral contraceptives. Prophylaxis for opportunistic infections, other than aerosolized pentamidine, topical antifungals, and TMP/SMX. Any other medication unless approved by Merck clinical monitor. Current illicit drug use.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Merck & Co Inc

Whitehouse Station, United StatesOpen Merck & Co Inc in Google Maps
CompletedOne Study Center