Completado

An Escalating Dose Tolerance Trial of BG8962 (rCD4) in Patients Who Are HIV Antibody Positive

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Qué se está evaluando

CD4 Antigens

Medicamento
Quiénes están siendo reclutados

Infecciones Transmitidas por la Sangre+13

+ Enfermedades Urogenitales

+ Enfermedades Genitales

A partir de 13 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Tratamiento

Fase 1
Intervencional
Ver detalles del protocolo

Resumen

Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 28 de octubre de 2021
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Recombinant soluble CD4 protein (rCD4) is a drug that has been produced by genetic engineering techniques. In laboratory studies, rCD4 binds to HIV and reduces its ability to enter the cell, thus inhibiting its reproduction. Before rCD4 can be tested for therapeutic effectiveness in HIV-infected patients, it is necessary to determine the maximum dose that can be tolerated by humans. AMENDED: To date, Biogen's original sequence recombinant soluble CD4 and Biogen's natural sequence recombinant soluble CD4 have both been referred to as recombinant soluble CD4 (rsCD4). In order to distinguish between these two products, a change in nomenclature has been made. In this protocol, whenever the original sequence CD4 molecule is referred to, it is called recombinant soluble T4 (rsT4). Whenever the natural sequence molecule (currently under study in this protocol) is referred to, it is called BG8962 or rCD4. Whenever the drug is discussed generically, it is referred to as rsCD4. The initial dose level is the highest dose previously established with other patients in this trial to be safe when administered intramuscularly (IM). Dose escalation is by semilogarithmic steps. A shift from IM injection to continuous subcutaneous infusion (CSCI) is necessitated by the volume of drug which is administered as part of the escalation dose. Three groups of eight patients each are treated as follows. The first group of 8 patients receives BG8962 daily and consists of two cohorts of four patients each. One cohort receives BG8962 as an IM injection. The second cohort receives BG8962 as a continuous 24 hour infusion. All patients in this group are treated for 12 weeks. The second dosing group of 8 patients receive daily BG8962 by CSCI for 12 weeks. The third group of 8 patients receive BG8962 by CSCI for 6 weeks. Every two weeks during the study the following tests and evaluations are done: Blood chemistry, hematology, urinalysis with microscopic exam, and T-cells and T-cell subsets.

NCT00000721
Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 28 de octubre de 2021
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 85 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Tratamiento

Estos estudios prueban nuevas formas de tratar una enfermedad, condición o problema de salud. El objetivo es determinar si un nuevo medicamento, terapia o enfoque funciona mejor o tiene menos efectos secundarios que las opciones existentes.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

A partir de 13 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos no permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Infecciones Transmitidas por la SangreEnfermedades UrogenitalesEnfermedades GenitalesEnfermedades TransmisiblesSíndromes de Deficiencia InmunológicaEnfermedades del sistema inmunitarioInfeccionesInfecciones por RetroviridaeInfecciones por virus de ARNEnfermedades de Transmisión SexualEnfermedades por virus lentoEnfermedades ViralesEnfermedades de transmisión sexual, viralesSíndrome de Inmunodeficiencia AdquiridaComplejo Relacionado con el SIDAInfecciones por VIH

Criterios

Inclusion Criteria Concurrent Medication: Allowed: Nystatin or clotrimazole for suppression of oral thrush. Aerosolized pentamidine for Pneumocystis prophylaxis in Group A patients. Trimethoprim / sulfamethoxazole for Pneumocystis prophylaxis in patients who are hematologically stable on trimethoprim / sulfamethoxazole. Patients must have: Group A: AIDS and symptoms defined in disease status. Group B: AIDS related complex (ARC) and symptoms defined in disease status. Exclusion Criteria Co-existing Condition: Patients with the following disease or conditions are excluded: Malignancies other than Kaposi's sarcoma. AIDS dementia. Opportunistic infections requiring ongoing therapy except oral thrush suppression with nystatin or clotrimazole or Pneumocystis prophylaxis in Group A patients. Significant organ system dysfunction including: Granulocytopenia with a granulocyte count < 1000 cells/mm3. Thrombocytopenia - < 75000 platelets/mm3. Anemia with a hemoglobin < 9.5 g/dl. Renal dysfunction - creatinine > 2 mg/dl. Hepatic dysfunction with enzymes or bilirubin > 3 x upper limit of normal. Patients with the following are excluded: Preexisting antibodies to rCD4. Malignancies other than Kaposi's sarcoma. AIDS-dementia complex. Opportunistic infections requiring ongoing therapy. Significant organ system dysfunction. Inability to sign voluntarily the consent form. Prior Medication: Excluded: Recombinant soluble CD4 protein (rCD4). Excluded within 30 days of study entry: Immunomodulatory therapy or agent with anti-HIV activity. Chemotherapy. Prior Treatment: Excluded within 30 days of study entry: Radiotherapy. Active illicit drug use or alcohol abuse at time of entry.

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene una ubicación

Stanford CRS

Palo Alto, United StatesAbrir Stanford CRS en Google Maps
Completado1 Centros de Estudio