- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07589205
Study of IBI3028 in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors
A Phase 1, Multi-Center, Open-Label Study Evaluating IBI3028 Treatment in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Yuxiao Xue
- Número de teléfono: (+86)18697486628
- Correo electrónico: yuxiao.xue@innoventbio.com
Ubicaciones de estudio
-
-
Tianjin Municipality
-
Tianjin, Tianjin Municipality, Porcelana, 300060
- Reclutamiento
- Tianjin Medical University Cancer Institute and Hospital
-
Investigador principal:
- Yi Hu
-
Investigador principal:
- Jihui Hao
-
Contacto:
- Jihui Hao
- Número de teléfono: 18622221120
- Correo electrónico: haojihui@tjmuch.com
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria
- Be able to understand and sign written informed consent to participate in this study, including all assessments and procedures specified in this protocol;
- Male or female participants aged 18 years or older;
- Have histologically or cytologically confirmed unresectable locally advanced or metastatic solid tumors;
- Have at least one evaluable lesion (dose escalation) or measurable lesion (dose expansion) as per RECIST v1.1 within 28 days prior to the first dose of IBI3028;
- ECOG PS(Eastern Cooperative Oncology Group Performance Status)score of 0-1;
- Anticipated life expectancy of ≥ 12 weeks;
Adequate bone marrow and organ function as evidenced by :
- Hematological function: ANC(Absolute neutrophil count) ≥ 1.5 × 10 9 /L; platelet count (PLT) ≥ 90 × 10 9 /L; hemoglobin ≥ 9.0 g/dL, and without receiving granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), thrombopoietin (TPO), interleukin-11, or other leukocyte/platelet stimulating growth factors (including red blood cell and platelet transfusions) within at least 7 days before the first dose of the study drug;
- Hepatic function: total bilirubin ≤ 1.5 × ULN (Upper Limit of Normal) (≤ 3 × ULN for participants with Gilbert's syndrome); AST(Aspartate Aminotransferase) and ALT (Alanine Aminotransferase)≤ 2.5 × ULN in the absence of liver metastases (≤ 5 × ULN if liver metastases are present); albumin ≥ 2.8 g/dL;
- Renal function: creatinine clearance ≥ 30 mL/min (using Cockcroft-Gault formula); urine protein < 2+ or 24-h total urine protein < 1 g;
- Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%, no clinically significant pericardial effusion as determined by ECHO or MUGA(Multigated Acquisition), and no clinically significant ECG result;
- Coagulation function: International normalized ratio (INR) ≤ 1.5; activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (participants receiving anticoagulant therapy with coagulation function within the range above are allowed);
- Pulmonary function: With at least the lowest level of pulmonary reserve, defined as Grade ≤ 1 dyspnea and blood oxygen saturation ≥ 95% in non-oxygen breathing state;
- Participants (both male and female participants) who will be not of childbearing potential or who agree to use at least 1 highly effective method of contraception during the study (from start of screening or within 2 weeks prior to first dose, whichever occurs first, and continue until 7 months for females and 4 months for males after the last dose of study drug).
Exclusion Criteria
- Participation in any other interventional clinical study other than an observational (non-interventional) study or during the follow-up period of an interventional study;
Prior anti-tumor therapy:
Participants who have received cytotoxic therapy within 3 weeks or 5 half-lives (whichever is shorter) prior to the first administration of study intervention ; Participants who have received PD-1/PD-L1 therapy within 4 weeks prior to the first administration of study drug; Participants who have received treatment with small molecule targeted therapy within 14 days or 5 half-lives (whichever is shorter) prior to the first dose of the study drug; Palliative radiation therapy within 2 weeks or radical radiation therapy within 4 weeks prior to the first dose of study drug; Participants who had received adoptive cell therapy within 8 weeks prior to the first administration of study intervention.
- Have received live vaccines within 4 weeks or tumor vaccines within 3 months prior to the first administration of the study drug, or plan to receive any live vaccines during the study;
- Use of strong cytochrome P450 3A4 (CYP3A4) enzyme inhibitors within 2 weeks or 5 half-lives (whichever is shorter) prior to the first dose of study drug;
- Adverse reactions caused by previous anti-tumor treatments that have not resolved to Grade 0 or 1 or baseline level according to NCI CTCAE v5.0 before the first dose of the study drug (except for alopecia, fatigue, pigmentation, and other conditions with no safety implications per the Investigator's clinical judgement);
- Known allergies, hypersensitivity, or intolerance to IBI3028 or its excipients (refer to the Investigator's Brochure);
- Have undergone major surgery (craniotomy, thoracotomy, or laparotomy, and other surgeries according to Investigators' opinion, excluding needle biopsy) within 4 weeks prior to the first dose of the investigational product, or are expected to undergo major surgery during the study, or have severe unhealed wounds, ulcers, etc.;
- Known symptomatic central nervous system (CNS) metastases. Participants with asymptomatic CNS metastases (ie, no neurologic syndrome and metastases ≤1.5 cm in diameter) or stable disease after treatment as judged by the investigator may be considered if: they have no metastases in the midbrain, pons, cerebellum, meninges, medulla oblongata, or spinal cord; stable status for at least 4 weeks prior to the first dose of study drug (≤1.5 mg/day dexamethasone or equivalent and baseline anticonvulsants are allowed), and have no new or enlarging CNS metastases as clearly demonstrated by clinical evidence; Note : CNS lesions are not considered target lesions.
Uncontrolled disease or condition, including:
- Uncontrolled infection requiring systemic antibiotics, antivirals, or antifungals prior to the first dose of the study drug;
- With known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Ab positive), for participants outside mainland China, participants with positive HIV antibody test at screening are eligible to participate in the study under the premise of undetectable viral load, or well-controlled under antiretroviral therapy (defined as CD4+ T cell count ≥ 350 cells/μL and no history of AIDS-defining opportunistic infection within 12 months before the first dose);
- Acute or chronic active hepatitis B (HBsAg positive and/or HBcAb positive, and HBV DNA titer ≥ 10 4 copies/mL or ≥ 2000 IU/mL) or hepatitis C (HCV Ab positive, and HCV RNA > 10 3 copies/mL or above the lower limit of detection);
- Active tuberculosis infection, or still receiving anti-tuberculosis treatment, or receiving anti-tuberculosis treatment within 1 year before the first dose of the study drug;
- Uncontrolled myocarditis or symptomatic congestive heart failure Class II-IV (New York Heart Association ,NYHA), symptomatic or uncontrolled arrhythmia, QTc interval > 480 ms, or personal or family history of congenital long/short QT syndrome;
- Uncontrolled hypertension with SBP ≥ 160 mmHg or DBP ≥ 100 mmHg measured on 2 follow-up visits despite adequate standard treatment;
- Current gastrointestinal tract (muscle-derived tube from the oral cavity to the anus, including oral cavity, pharynx, esophagus, stomach, duodenum, jejunum, ileum, cecum, appendix, colon, rectum, and anus) or endotracheal stent implantation;
- Significant malnutrition, such as malnutrition requiring parenteral nutrition;
- Spinal cord compression that has not been radically cured by surgery and/or radiotherapy;
- Ascites, pleural effusion, or pericardial effusion that is symptomatic and requires intervention prior to the first dose of study intervention (participants who do not require treatment or who recover steadily without intervention are eligible).
- With a history of pneumonia requiring corticosteroid treatment, or a history of clinically significant lung diseases (such as interstitial lung disease, non-infectious pneumonitis, or uncontrolled lung diseases such as pulmonary fibrosis, severe radiation pneumonitis, and acute lung injury), or suspected of having these diseases by imaging during the screening period;
- Any history of arterial thromboembolic events within 6 months prior to the first dose of the study drug, including myocardial infarction, unstable angina, cerebrovascular stroke, or transient ischemic attack;
- Esophageal or gastric varices requiring immediate intervention (e.g., ligature or sclerotherapy) or at high risk of bleeding according to the opinion of the investigator or a gastroenterologist or hepatologist. Participants with evidence of portal hypertension (including imaging findings of hypersplenism) or a history of esophageal and gastric variceal bleeding must undergo endoscopic evaluation within 3 months prior to the first dose of the study drug;
- Any history of life-threatening hemorrhage or hemorrhage requiring blood transfusion, endoscopy, or surgery within 3 months prior to the first dose of the investigational product ;
- Unhealed gastrointestinal obstruction, perforation, or fistula. At risk of gastrointestinal obstruction or perforation (including but not limited to: acute diverticulitis, abdominal abscess, etc.), history of extensive bowel resection (segmental colectomy or extensive bowel resection accompanied with chronic diarrhea), active inflammatory bowel disease, or Grade ≥ 2 chronic diarrhea;
- History of immunodeficiency diseases, including congenital or acquired immunodeficiency diseases;
- History of allogeneic organ transplantation or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation within 3 months prior to the first dose of the investigational drug, except for corneal transplantation;
History of other malignancy within 2 years before the first dose of study drug(s), with the following exceptions:
- Malignancy (other than in situ) treated with curative therapy with no known active disease present for ≥ 2 years prior to the first dose of study drug and at low risk of recurrence according to the physician's opinion;
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of residual or recurrent disease;
- Adequately treated carcinoma in situ without evidence of residual or recurrent disease;
- Prostate intraepithelial neoplasia without evidence of prostate cancer;
- Adequately treated urothelial papillary non-invasive carcinoma.
- Presence of any indwelling tubes or drains (such as percutaneous nephrostomy tubes, indwelling Foley catheters, biliary drainage tubes, or peritoneal/pericardial catheters); Note: Thoracic catheters or dedicated central venous access catheters such as Port-A-Cath or Hickman catheters are allowed.
- Other acute or chronic diseases or laboratory abnormalities, which may increase the risk of participating in the study or receiving the investigational product, interfere with the interpretation of study results, and make the participant unsuitable for participating in the study based on the investigator's judgment;
- Neurological, mental, or social conditions that affect the compliance with trial requirements, significantly increase the risk of AEs, or affect the participants' signing of written informed consent (IC);
- Females who are pregnant, have a positive pregnancy test result, or are breastfeeding;
- Not fit to participate in this study at the discretion of the Investigator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Drug: IBI3028
IBI3028 will be dosed until disease progression, toxicity intolerance, starting of new systemic anti-cancer treatment, withdrawal of consent, occurrence of other reasons for discontinuing study therapy, or treatment duration reaching the maximum of 24 months, whichever occurs first.
|
Recombinant anti-EGFR(Epidermal growth factor receptor) and c-Met antibodies-dual-payload conjugate for injection
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Número de sujetos con cambios clínicamente significativos en los resultados del examen físico
Periodo de tiempo: Hasta 3 años
|
Hallazgos anormales clínicamente significativos en el examen físico informados por el investigador.
|
Hasta 3 años
|
|
Número de sujetos con cambios clínicamente significativos en el electrocardiograma
Periodo de tiempo: Hasta 3 años
|
Hallazgos anormales clínicamente significativos del electrocardiograma informados por el investigador.
|
Hasta 3 años
|
|
Número de sujetos con cambios clínicamente significativos en los signos vitales
Periodo de tiempo: Hasta 3 años
|
Signos vitales que incluyen temperatura corporal, pulso, velocidad respiratoria, saturación de oxígeno por oximetría de pulso en reposo y presión arterial
|
Hasta 3 años
|
|
Toxicidades que limitan la dosis (DLT)
Periodo de tiempo: Hasta 21 días
|
Toxicidades limitantes de dosis (DLT) para establecer MTD y/o RP2D.
|
Hasta 21 días
|
|
Número de sujetos con cambios clínicamente significativos en los parámetros de laboratorio
Periodo de tiempo: Hasta 3 años
|
Hallazgos de parámetros de laboratorio anormales clínicamente significativos informados por el investigador.
|
Hasta 3 años
|
|
Numbers of subjects with adverse events
Periodo de tiempo: Up to 3 years
|
Defined as any untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
|
Up to 3 years
|
|
Numbers of subjects with serious adverse events
Periodo de tiempo: Up to 3 years
|
Defined as any serious untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
|
Up to 3 years
|
|
Number of AEs(adverse events) leading to dose interruption
Periodo de tiempo: Up to 3 years
|
AEs(adverse events) leading to dose interruption reported by the investigator
|
Up to 3 years
|
|
Number of AEs leading to dose delay
Periodo de tiempo: Up to 3 years
|
AEs leading to dose delay reported by the investigator
|
Up to 3 years
|
|
Number of AEs leading to dose reduction
Periodo de tiempo: Up to 3 years
|
AEs leading to dose reduction reported by the investigator
|
Up to 3 years
|
|
Number of AEs leading to permanent discontinuation
Periodo de tiempo: Up to 3 years
|
AEs leading to permanent discontinuation reported by the investigator
|
Up to 3 years
|
|
Objective response rate (ORR) in dose expansion
Periodo de tiempo: Up to 3 years
|
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria.
|
Up to 3 years
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Area under the curve (AUC)
Periodo de tiempo: Up to 3 years
|
Area under the curve (AUC) of single and multiple doses of IBI3028
|
Up to 3 years
|
|
Maximum concentration (Cmax)
Periodo de tiempo: Up to 3 years
|
Maximum concentration (Cmax) of single and multiple doses of IBI3028
|
Up to 3 years
|
|
Time to maximum concentration (Tmax)
Periodo de tiempo: Up to 3 years
|
Time to maximum concentration (Tmax) of single and multiple doses of IBI3028
|
Up to 3 years
|
|
Clearance (CL)
Periodo de tiempo: Up to 3 years
|
Clearance (CL) of single and multiple doses of IBI3028
|
Up to 3 years
|
|
Apparent volume of distribution (V)
Periodo de tiempo: Up to 3 years
|
apparent volume of distribution (V) of single and multiple doses of IBI3028
|
Up to 3 years
|
|
Half-life (t1/2)
Periodo de tiempo: Up to 3 years
|
Half-life (t1/2) of IBI3020 to the last administration of IBI3028
|
Up to 3 years
|
|
Anti-drug antibody (ADA)
Periodo de tiempo: Up to 3 years
|
Incidence and characterization of anti-drug antibody (ADA)
|
Up to 3 years
|
|
Neutralizing antibody (NAb)
Periodo de tiempo: Up to 3 years
|
Incidence and characterization of neutralizing antibody (NAb)
|
Up to 3 years
|
|
Objective response rate (ORR)
Periodo de tiempo: Up to 3 years
|
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria
|
Up to 3 years
|
|
Duration of response (DoR)
Periodo de tiempo: Up to 3 years
|
Duration of response (DoR) as evaluated per the RECIST v1.1 criteria
|
Up to 3 years
|
|
Disease control rate (DCR)
Periodo de tiempo: Up to 3 years
|
Disease control rate (DCR) as evaluated per the RECIST v1.1 criteria
|
Up to 3 years
|
|
Time to response (TTR)
Periodo de tiempo: Up to 3 years
|
Time to response (TTR) as evaluated per the RECIST v1.1 criteria
|
Up to 3 years
|
|
Progression-free survival (PFS)
Periodo de tiempo: Up to 3 years
|
progression-free survival (PFS) as evaluated per the RECIST v1.1 criteria
|
Up to 3 years
|
|
Overall survival (OS)
Periodo de tiempo: Up to 3 years
|
OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
|
Up to 3 years
|
Colaboradores e Investigadores
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
Términos MeSH relevantes adicionales
- Neoplasias por sitio
- Neoplasias
- Enfermedades intestinales
- Enfermedades de las vías respiratorias
- Neoplasias por tipo histológico
- Neoplasias Gastrointestinales
- Neoplasias del Sistema Digestivo
- Enfermedades del Sistema Digestivo
- Enfermedades Gastrointestinales
- Neoplasias Intestinales
- Enfermedades Rectales
- Enfermedades pulmonares
- Neoplasias de Cabeza y Cuello
- Neoplasias Glandulares y Epiteliales
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Enfermedades del Colon
- Neoplasias Pulmonares
- Carcinoma
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Carcinoma De Células Escamosas
- Carcinoma de células escamosas de cabeza y cuello
- Neoplasias colorrectales
- Carcinoma de pulmón de células no pequeñas
Otros números de identificación del estudio
- CIBI3028A101
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. .
Ensayos clínicos sobre Cáncer colonrectal
-
Istanbul Aydın UniversityTerminado
-
Abramson Cancer Center of the University of PennsylvaniaTerminadoPaciente con cancerEstados Unidos
-
Peking Union Medical College HospitalTerminadoEncuesta | Estado nutricional | Paciente con cancerPorcelana
-
Northwestern UniversityGenzyme, a Sanofi CompanyRetiradoCANCER DE PROSTATAEstados Unidos
-
Ankara Medipol UniversityReclutamientoCuidados personales | Inmunoterapia | Manejo de síntomas | Paciente con cancerPavo
-
Fundacao ChampalimaudTerminado
-
University College London HospitalsTerminado
-
GenSpera, Inc.RetiradoCancer de prostata.Estados Unidos
-
University of Colorado, DenverColorado State UniversityRetiradoRealidad virtual | Diagnóstico por imagen | Educación del paciente | Paciente con cancerEstados Unidos
-
Dana-Farber Cancer InstituteTerminadoCancer de RIÑON | Cancer de prostata | Cáncer genitourinarioEstados Unidos
Ensayos clínicos sobre Drug: IBI3028
-
Chinese PLA General HospitalAún no reclutando
-
Skane University HospitalTerminadoEnfermedades Vasculares
-
Lyra TherapeuticsTerminadoSinusitis crónicaNueva Zelanda, Australia
-
Mclean HospitalNational Institute on Drug Abuse (NIDA)TerminadoDependencia del cannabis | Dependencia de la marihuanaEstados Unidos
-
Washington University School of MedicineTerminadoFilariasis linfatica | Oncocercosis | Infecciones por helmintos transmitidos por el suelo (STH)Liberia
-
Laboratorios Andromaco S.A.Terminado
-
Kurume UniversityEisai Inc.; Mebix IncTerminado
-
Omer KaracaBaskent UniversityTerminadoTerapia de ultrasonido; ComplicacionesPavo
-
Mclean HospitalBrain & Behavior Research FoundationTerminadoDependencia del cannabis | Dependencia de la marihuanaEstados Unidos