- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00319930
Phase 1, Dose-Escalation, Pharmacodynamic Study of IV CNF1010 in ZAP-70 Positive CLL
A Phase 1, Multi-Center, Open-Label, Dose-Escalation, Pharmacodynamic Study of Intravenously Administered CNF1010 (17-(Allylamino)-17-demethoxy-geldanamycin [17-AAG]) in Patients With ZAP-70 Positive B-Cell Chronic Lymphocytic Leukemia (CLL)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Florida
-
Ocoee, Florida, Estados Unidos, 34761
-
-
New York
-
Albany, New York, Estados Unidos, 12208
-
-
Ohio
-
Dayton, Ohio, Estados Unidos, 45409
-
-
South Carolina
-
Greenville, South Carolina, Estados Unidos, 29605
-
-
Texas
-
Tyler, Texas, Estados Unidos, 75702
-
-
Virginia
-
Norfolk, Virginia, Estados Unidos, 85258
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Key Inclusion Criteria:
Diagnosis of B-cell CLL including
- Lymphocytosis of >=5,000 monoclonal B-cells/microliter co-expressing >= one B-cell marker (CD19, CD20, or CD23) and CD5 in peripheral blood AND
- <= 55% prolymphocytes AND
- Bone marrow with >=30% mononuclear cells being lymphocytes
- ZAP-70 positive CLL
Intermediate or High risk, poor prognosis CLL refractory to fludarabine-based therapy as defined by one of the following:
- Disease progression following 2 cycles of fludarabine OR
- Failure to achieve PR or CR after at least 2 cycles OR
- No response to treatment or stable disease after at least 2 cycles of fludarabine OR
- Disease progression after chemotherapy treatment after fludarabine-based therapy
OR
· CLL patients intolerant to fludarabine-based therapy. [Intolerance is defined as the development of any serious medical condition occurring after exposure to fludarabine that would restrict further use of the agent as treatment for the patient's CLL (i.e., autoimmune hemolytic anemia, myelosuppression, hypersensitivity)]
- Indication for treatment as defined by the NCI Working Group Guidelines
Laboratory parameters as follows:
- Hemoglobin >=10 g/dL (may be post-transfusion); platelet count >=50 x103/mm3
- T. Bili <2 x ULN and ALT and AST <2 x ULN
- Creatinine <=2 x ULN
- ECOG Performance Score <=2
- For patients of child-producing potential, use of effective contraceptive methods during the study and for 1 month following treatment
Key Exclusion Criteria:
- Pregnant or nursing women
- Class III or IV cardiac disease defined by the New York Heart Association Functional Classification and/or left ventricular ejection fraction <40%
- History of prior radiation that potentially included the heart in the field.
- History of myocardial infarction or active ischemic heart disease within 6 months of study entry
- History of arrhythmia (including atrial fibrillation, multifocal premature ventricular contractions, ventricular bigeminy or trigeminy, ventricular tachycardia or a requirement for antiarrhythmics (including digoxin)
- Baseline QTc >=450 msec for men and >= 470 msec for women in the absence of correctable electrolyte imbalance
- Poorly controlled angina
- Congenital long QT syndrome or first-degree relative with unexplained sudden death <40 years of age
- Presence of left bundle branch block
- Treatment with chemotherapy, monoclonal antibody or radiotherapy within 28 days of study entry
- Severe or debilitating pulmonary disease
- Participation in any investigational drug study within 28 days prior to CNF1010 administration. (Patient must have recovered from all acute effects of previously administered investigational agents)
- Presence of active malignancy with the exception of basal cell carcinoma
- Active symptomatic fungal, bacterial and/or viral infection including active HIV or viral (A, B or C) hepatitis
- Known allergy to soy
- Requirement for concomitant therapy with drugs that alter metabolism by cytochrome P450 3A4 except low-dose warfarin for implanted device patency
- Requirement for concomitant therapy with drugs that prolong or may prolong QTc interval
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
|---|
|
Farmacocinética (PK)
|
|
Pharmacodynamics (PD)
|
|
The minimal biologically active dose (MBAD)
|
|
Safety and toxicity profile
|
|
Clinical and hematological response
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- CNF1010-CLL-05001
- 110CL101
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .