Clinical Study of Oral IGF-1R Inhibitor in Subjects With Advanced Refractory Solid Tumors
An Open Label Multicentre Phase 1 Study of Oral IGF-1R Inhibitor PL225B in Subjects With Advanced Refractory Solid Tumors.
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Tipo de estudio
Inscripción (Anticipado)
Inscripción
Fase
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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California
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Los Angeles, California, Estados Unidos, 90033
- USC Norris Comprehensive Cancer Center
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Maharashtra
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Nagpur, Maharashtra, India, 440010
- Central India Cancer Research Institute
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Nashik, Maharashtra, India, 422004
- Curie Manavata Cancer Centre
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Pune, Maharashtra, India, 411001
- Ruby Hall Clinic
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Tamil Nadu
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Madurai, Tamil Nadu, India, 625107
- Meenakshi Mission Hospital and Research Centre
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Subjects having histologically and/or cytologically confirmed non-haematological malignancy that is metastatic or unresectable and for which standard curative or palliative treatment does not exist or is no longer effective
- Subjects should have measurable or evaluable disease
- Subjects of either sex, of all races and ethnic groups, and ≥18 years of age
- ECOG (Eastern Cooperative Oncology Group) performance status 0-1
- Subjects with life expectancy of at least 4 months
- Subjects with fasting plasma glucose ≤ 125 mg/dL and HbA1c < 6.5 % at screening Subjects with fasting plasma glucose ≤150 mg/dL and HbA1c ≤ 7.0 % at screening for the Diabetes Expansion Cohort.
- For the Diabetes Expansion Cohort - Subjects with known history of type 2 diabetes mellitus that are well-controlled on a stable dose of oral anti-diabetic agents such as metformin and/or sulfonylureas for 4 weeks prior to screening.
Subjects must have normal organ and marrow function as defined below:
- Absolute neutrophil count ≥ 1500/cmm
- Platelets ≥ 100,000/cmm
- Total bilirubinwithin normal limits of the institution
- AST/ALT ≤ 2.5 X institutional upper limit of normal (ULN) or ≤ 5 X institutional upper limit of normal (ULN) in the presence of liver metastases
- Creatinine ≤ 1.5 X institutional upper limit of normal (ULN)
- Subjects willing for repeat oral dosing and follow-up, including pharmacokinetic sampling
- Women of childbearing potential and men willing to agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, during the duration of study participation and for at least 4 weeks after withdrawal from the study, unless they are surgically sterilised
- Ability to understand and the willingness to provide a written informed consent document
Exclusion Criteria
- Subjects who have received any prior chemotherapy, radiotherapy, biologic/targeted anti-cancer therapy or surgery within 4 weeks (6 weeks for monoclonal antibodies, radioactive monoclonal antibodies or any radio- or toxin- immunoconjugates) before the first study drug administration and have not recovered (to AEs < Grade 2) from the toxic effects from any prior therapy
- Subjects having received any other investigational agents within 4 weeks prior to the first study drug administration and have not recovered completely (to AEs < Grade 2) from the side effects of the earlier investigational agent
- Subjects with documented history of diabetes mellitus except for the Diabetes Expansion Cohort
- For the Diabetes Expansion Cohort - Subjects who have type 1 diabetes mellitus, maturity onset diabetes of the young, hyperglycemia due to reasons other than type 2 diabetes mellitus.
- For the Diabetes Expansion Cohort - Subjects who currently require insulin, thiazolidinediones, dual proliferator-activated receptors (PPAR) agonists, glucagon-like peptide (GLP-1) analogues, dipeptidyl peptidase (DPP-IV) inhibitors or have received the same in the 4 weeks prior to screening.
- Subjects with known complications of diabetes like diabetic nephropathy or diabetic retinopathy
- Subjects with known brain metastases
- Subjects with gastrointestinal abnormalities including inability to take oral medication, malabsorption or other conditions like chronic inflammatory bowel disease that may affect absorption.
- Subjects with a history of myocardial infarction or uncontrolled cardiac dysfunction during the previous 6 months
- Subjects with baseline QTc interval >470 msec at screening
- Subjects on warfarin. Prophylactic anticoagulation with low molecular weight heparin is allowed
- Subjects with history of anaphylaxis or angioedema, bronchial asthma, peptic ulcer and clinically significant food or drug allergy
- Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Women who are pregnant or nursing
- Subjects with known seropositivity to human immunodeficiency virus (HIV), positive for Hepatitis B, positive for Hepatitis C (antigen positive), or known hepatic cirrhosis
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
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Experimental: PL225B
Patients will receive study drug on a daily basis until disease progression or unacceptable toxicity in sequential cohorts following accelerated titration design.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Maximum tolerated dose
Periodo de tiempo: End of Cycle 1 (i.e. 21 Days)
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Subjects will receive study drug on a daily basis for twenty-one (21) days according to the dose and schedule specified for a particular cohort of therapy.Toxicity profile of the drug will be assessed during Cycle 1 of subject treatment in each cohort for determination of Maximum Tolerated Dose (MTD).
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End of Cycle 1 (i.e. 21 Days)
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Número de sujetos con eventos adversos
Periodo de tiempo: Hasta progresión de la enfermedad o toxicidad inaceptable (se espera que sea de 4 a 6 meses)
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Los efectos tóxicos del fármaco se evaluarían a partir de eventos adversos, signos vitales y cambios clínicamente significativos en las evaluaciones de laboratorio.
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Hasta progresión de la enfermedad o toxicidad inaceptable (se espera que sea de 4 a 6 meses)
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Respuesta objetiva
Periodo de tiempo: Hasta progresión de la enfermedad o toxicidad inaceptable (se espera que sea de 4 a 6 meses)
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Evaluación de la respuesta: las respuestas clínicas se presentarán según el paciente para diferentes niveles de dosis.
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Hasta progresión de la enfermedad o toxicidad inaceptable (se espera que sea de 4 a 6 meses)
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Pharmacokinetic profile(Cmax,Tmax and AUC)
Periodo de tiempo: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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The following PK parameters will be calculated: Cmax (peak plasma concentration), Tmax (time to peak plasma concentration), AUC0-t (area under the plasma concentration curve from time zero to time of last quantifiable concentration), AUC0-12, AUC0-inf (area under the plasma concentration curve from time zero extrapolated to infinity), percent AUC extrapolated, kel (elimination rate constant), t1/2 (elimination half-life), CL/F (oral clearance), Vz/F (oral apparent volume of distribution) and Racc (accumulation ratio).
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Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Activity of PL225B based on selected biomarkers
Periodo de tiempo: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Plasma samples will be used for analysis of circulating exploratory biomarkers which are likely to change in response to PL225B administration.
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Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Dr Anthony El-Khoueiry, MD, University of Southern California
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización primaria
Finalización del estudio (Anticipado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- PL225B/71/11
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