- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07646106
THE-0504 in Patients With Solid Tumors
NANOFER-THE-0504: A Trial to Assess the Safety and Tolerability of an Investigational Drug THE-0504 for Patients With Solid Tumors
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Pierpaolo Ceci, PhD
- Número de teléfono: +39 0773822658
- Correo electrónico: pierpaolo.ceci@thenabiotech.com
Copia de seguridad de contactos de estudio
- Nombre: Gennaro Daniele, PhD
- Número de teléfono: +39 0630157300
- Correo electrónico: gennaro.daniele@policlinicogemelli.it
Ubicaciones de estudio
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-
Lazio
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Rome, Lazio, Italia, 00168
- Reclutamiento
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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Contacto:
- Gennaro Daniele, PhD
- Número de teléfono: +39 0630157300
- Correo electrónico: gennaro.daniele@policlinicogemelli.it
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
Patients will be enrolled in the study if they meet all the following criteria:
- written informed consent obtained;
- both gender adult (≥ 18 years) patients;
- diagnosis of solid tumor. Preferably, but non-limited, tumor types are the following: Small Cell Lung Cancer (SCLC), Colorectal Carcinoma (CRC), Pancreas Adenocarcinoma (PaAdCa), Gastric Cancer (GC) and Triple Negative Breast Cancer (TNBrCa);
- measurable metastatic disease or locally advanced unresectable tumors;
- have exhausted all EMA-approved treatment options;
- ECOG Performance Status graded as 0 or 1;
- patients able to understand the full nature and the purpose of the trial, including possible risks and side effects, able to cooperate with the Investigator and to comply with the requirements of the entire trial (ability to attend all the planned trial visits according to the time limits included) based on Investigator's judgement;
adequate liver function as assessed by following laboratory tests to be conducted within 28 days before the first dose of study treatment:
- Total bilirubin ≤ 1.5 × ULN (or ≤ 3 X ULN for patients with documented Gilbert-Meulengracht Syndrome, or for patients with hyperbilirubinemia considered due to liver metastasis).
- Aspartate transaminase and alanine transaminase ≤ 2.5 × ULN (or ≤ 5 × ULN if due to liver involvement by tumor);
adequate kidney function as assessed by following laboratory test to be conducted within 28 days before the first dose of study treatment:
• Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min per 1.73 m2 according to the CKD-EPI formula.
adequate bone marrow function as defined as:
- Hgb ≥ 9 g/dL
- ANC ≥1.5x109/L
- PLT≥100.0 x109/L
- Female patients of childbearing potential and male patients who are sexually active with women of childbearing potential will have to mandatorily use an appropriate method of contraception, according to the definition of Note 3 of ICH M3 Guideline, for the entire duration of the trial and for a minimum of 12 months after last administration of the IMP.
Exclusion Criteria:
Patients will not be enrolled if they meet any of the following criteria:
- pregnant (as determined by a blood pregnancy test at the screening visit) or lactating women;
- male patients who are willing to father children during the trial or in the 12 months after the end of IMP administration;
- additional malignancy in the last 5 years. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or in situ cervical cancer that has undergone potentially curative therapy;
- have any unresolved toxicity of Grade ≥ 2 from previous anti-cancer treatment, except for alopecia and skin pigmentation. Patients with chronic, but stable Grade 2 toxicities may be allowed to enrol after agreement between the Investigator and Sponsor;
- ECOG Performance Status > 2;
- had not tolerated previously administered Top1 inhibitor treatments;
- known active CNS metastatic disease (patients with CNS metastases that are treated with radiotherapy and are stable for at least 28 days before study treatment start could be considered eligible);
- serious concurrent illness;
- Hgb < 9 g/dL;
- Transfusion dependent anemia with transfusion dependency of ≥3 months;
- Clinically significant iron metabolism disorders (e.g., sickle cell anemia) or use of iron chelators treatments;
- Iron overload, hereditary hemochromatosis and similar;
- Moderate (Child-Pugh B) or severe (Child-Pugh C) hepatic impairment;
- Prolonged QTc interval;
- Multiple Sclerosis (MS) or other demyelinating disease, Eaton-Lambert syndrome, history of haemorrhagic or ischemic stroke within the last 6 months, or alcoholic liver disease;
- Non-healing wound(s), except for ulcerative lesions caused by the underlying neoplasm;
- History of severe allergic or anaphylactic reactions to previous protein-based therapy;
- Currently receiving anticoagulation therapy with warfarin;
Known history of HIV infection, unless all the following are applicable:
- receiving an approved, stable, effective combination antiretroviral therapy regimen for ≥ 3 months prior to the planned first study intervention;
- CD4 T-cell count > 350 cells/μL
- CD4 T-cell nadir (lowest historical count) > 350 cells/μL, and • viral load confirmed as < 50 copies/mL.
- HBV infection, unless on stable anti-viral therapy for > 4 weeks prior to the planned first dose of study intervention and viral load confirmed as undetectable; and HCV infection, unless the participant has received curative treatment and viral load was confirmed as undetectable;
- Known autoimmune disease, uncontrolled diabetes, vitiligo, or stable thyroid disease;
- Patients on chronic (more than 10 days) administration of systemic, high-dose corticosteroids (≥4 mg Dexamethasone or equivalent), not amenable for reduction or suspension;
- Other concurrent medical or psychiatric conditions that, in the Investigator's opinion, may be likely to confound study interpretation or prevent completion of study procedures and follow-up examinations;
- History of drugs and/or alcohol abuse;
- Patients considered to be unsuitable to participate, in the Investigator's opinion, for any other reason (e.g. consequences of previous medical and/or surgical procedures or other medical or ethical reasons);
- Planned relocation during the study, which would make impossible to attend the scheduled visits and follow-ups;
- Concomitant participation in other clinical trials or participation in the evaluation of any investigational drugs/products up to 4 weeks before this trial (in any case, enrolment procedure should start only after the complete washout of the drugs/products under investigation**); or previous participation in the same trial or planned to receive other investigational products during the study.
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)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Brazo de tratamiento
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THE-0504 will be administered intravenously according to the treatment regimen specified in the protocol.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Assessment of Maximum Tolerated Dose (MTD)
Periodo de tiempo: From enrollment to completion of Cycle 1 (each cycle is 21 days)
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From enrollment to completion of Cycle 1 (each cycle is 21 days)
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Assessment of Recommended Phase 2 Dose (RP2D)
Periodo de tiempo: During dose escalation, at the end of cycle 1 (each cycle is 21 days)
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During dose escalation, at the end of cycle 1 (each cycle is 21 days)
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Pharmacokinetic assessments of the IMP
Periodo de tiempo: Pre-dose and up to 96 hours (30 minutes, 3 hours, 24 hours, 48 hours and 96 hours) post-dose of the first 3 Cycles (63 days)
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Pre-dose and up to 96 hours (30 minutes, 3 hours, 24 hours, 48 hours and 96 hours) post-dose of the first 3 Cycles (63 days)
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Uprising / incidence of anti-THE-05 antibodies (ADA)
Periodo de tiempo: From baseline through Cycle 4 (84 days)
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From baseline through Cycle 4 (84 days)
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Objective Response Rate (ORR) according to RECIST 1.1
Periodo de tiempo: From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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Progression-Free Survival (PFS)
Periodo de tiempo: From enrollment until disease progression or death from any cause (assessed up to 36 months)
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From enrollment until disease progression or death from any cause (assessed up to 36 months)
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Overall Survival (OS)
Periodo de tiempo: From first IMP administration until death from any cause (assessed up to 36 months)
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From first IMP administration until death from any cause (assessed up to 36 months)
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Rate of patients with Complete Response (CR) or Partial Response (PR) according to RECIST 1.1
Periodo de tiempo: From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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From baseline until disease progression, death, withdrawal or initiation of subsequent anticancer therapy (assessed up to 36 months)
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Assessment of safety profile of the product THE-0504
Periodo de tiempo: From first IMP administration through 90 days after last IMP administration
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From first IMP administration through 90 days after last IMP administration
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ECOG Performance Status changes from baseline
Periodo de tiempo: From baseline through 90 days after last IMP administration
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From baseline through 90 days after last IMP administration
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Gennaro Daniele, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
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
- Neoplasias por sitio
- Enfermedades intestinales
- Enfermedades de las vías respiratorias
- Neoplasias Gastrointestinales
- Neoplasias del Sistema Digestivo
- Enfermedades del Sistema Digestivo
- Enfermedades Gastrointestinales
- Enfermedades del Estómago
- Neoplasias Intestinales
- Enfermedades Rectales
- Enfermedades pulmonares
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Enfermedades del Colon
- Neoplasias Pulmonares
- Enfermedades de la piel
- Enfermedades de los senos
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Neoplasias de mama
- Enfermedades de la piel y del tejido conectivo
- Neoplasias
- Neoplasias de Estómago
- Neoplasias colorrectales
- Carcinoma de pulmón de células pequeñas
- Neoplasias mamarias triple negativas
Otros números de identificación del estudio
- THE-0504-001
- 2023-503787-17-00 (Ctis)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
To the present date, only the sharing of the summary of the clinical results after 30 months from the study completion can be guaranteed.
Complete data from individual participants cannot be shared in scientific publications until intellectual property of the Investigational Medicinal Product is granted in all countries currently under evaluation.
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .