- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07224425
Un estudio en personas con cáncer avanzado (tumores sólidos) para probar diferentes dosis de BI 3810944 y determinar si resulta beneficioso
Un Estudio de Primera Aplicación en Humanos, Fase I, Abierto, No Aleatorizado, Multicéntrico de Escalación de Dosis y Expansión de BI 3810944 en Pacientes con Tumores Sólidos y Melanoma
This study is open to adults with advanced cancer (solid tumours) for whom previous treatment was not successful, or no treatment exists. The study tests different doses of BI 3810944 to find out which doses they can tolerate. Another purpose is to identify the most suitable dose of BI 3810944 and to find out whether it helps people with advanced cancer.
Participants get BI 3810944 usually once every 3 weeks. At treatment start, it is given once a week for a short time. Participants may continue to get BI 3810944 as long as they benefit from treatment. The treatment duration is planned for 2 years. During this time, they regularly visit the study site. The first study visits include overnight stays at the hospital. At the visits, study doctors check participants' health, take necessary laboratory tests, and note any unwanted effects.
The doctors also regularly check the size of the tumour with imaging methods.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Boehringer Ingelheim
- Número de teléfono: 1-800-243-0127
- Correo electrónico: clintriage.rdg@boehringer-ingelheim.com
Ubicaciones de estudio
-
-
-
Brussels, Bélgica, 1200
- Reclutamiento
- Cliniques Universitaires Saint-Luc
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 080049616
- Correo electrónico: belgique@bitrialsupport.com
-
Leuven, Bélgica, 3000
- Reclutamiento
- UZ Leuven
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 080049616
- Correo electrónico: belgique@bitrialsupport.com
-
-
-
-
Kentucky
-
Louisville, Kentucky, Estados Unidos, 40202
- Reclutamiento
- University of Louisville
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 833-602-2368
- Correo electrónico: unitedstates@bitrialsupport.com
-
-
Tennessee
-
Nashville, Tennessee, Estados Unidos, 37203
- Reclutamiento
- Tennessee Oncology, PLLC - Elliston Place Plaza DDU
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 833-602-2368
- Correo electrónico: unitedstates@bitrialsupport.com
-
-
Texas
-
Houston, Texas, Estados Unidos, 77030
- Aún no reclutando
- The University of Texas MD Anderson Cancer Center
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 833-602-2368
- Correo electrónico: unitedstates@bitrialsupport.com
-
-
Virginia
-
Charlottesville, Virginia, Estados Unidos, 22908
- Aún no reclutando
- University of Virginia Health System
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 833-602-2368
- Correo electrónico: unitedstates@bitrialsupport.com
-
-
-
-
-
Nijmegen, Países Bajos, 6525 GA
- Reclutamiento
- Radboud Universitair Medisch Centrum
-
Contacto:
- Boehringer Ingelheim
- Número de teléfono: 08000204613
- Correo electrónico: nederland@bitrialsupport.com
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
-
Trial participant population specifically to Part A and B:
- Part A only: participants with any histologically or cytologically confirmed diagnosis of solid tumour who failed conventional treatment or for whom no therapy of proven efficacy exists or who is not eligible for established treatment options. Participant must have exhausted available treatment options known to prolong survival for their disease.
- Part B only: participants with histologically or cytologically confirmed diagnosis of who has progressed on, or is intolerant to available standard therapies, or for whom no standard therapy with proven benefit exists according to the local and institutional guidelines. Participants should not have received >3 previous lines of treatment (excluding prior systemic regimens received at adjuvant or neoadjuvant setting and excluding treatment with tumour-infiltrating lymphocytes at any timepoint). B-raf protein kinase (BRAF) mutation status must be known prior to screening
-
Eastern cooperative oncology group (ECOG) performance status of 0 or 1
-
Presence of at least one measurable lesion outside of central nervous system (CNS) as defined per response evaluation criteria in solid tumours (RECIST v 1.1)
-
Age ≥18 years
-
Adequate organ function
-
Life expectancy of ≥3 months at the start of the trial treatment in the opinion of the investigator
-
All toxicities related to previous anticancer therapies have resolved to common terminology criteria for adverse events (CTCAE) Grade ≤1 prior to trial treatment administration (except for alopecia and peripheral neuropathy which must be CTCAE Grade ≤2 and amenorrhea/menstrual disorders which can be any Grade) Further inclusion criteria apply.
Exclusion Criteria:
-
Active primary central nervous system (CNS) malignancy, active untreated CNS metastases and/or carcinomatous meningitis
-
Participants with asymptomatic (i.e. no clinical neurological symptoms) brain lesions are eligible provided they meet the following criteria:
- Radiotherapy or surgery for brain metastases was completed ≥2 weeks before the first administration of BI 3810944
- Patient is off steroids for ≥7 days (physiologic doses of steroids are permitted), and the patient is off anti-epileptic drugs for ≥7 days or on stable doses of anti-epileptic drugs for malignant CNS disease
-
-
A diagnosis of immunodeficiency; receiving chronic systemic therapy exceeding prednisone 10 mg daily or equivalent or any other form of immunosuppressive therapy within 7 days before the step-up dose of BI 3810944
-
Prior anticancer therapy:
- Participants who have been treated with any other anticancer drug(s), within 28 days or within 5 half-life periods (whichever is shorter) prior to the first administration of BI 3810944
- Participants who have been treated with extensive field radiotherapy including whole brain irradiation, within 2 weeks prior to first administration of BI 3810944
-
Prior treatment with organ transplant or allogenic hematopoietic stem-cell transplant
-
Anticoagulant treatment that cannot be safely interrupted based on opinion of the investigator if medically needed (e.g. biopsy)
-
Women who are pregnant, breastfeeding or who plan to become pregnant or breastfeeding during the trial or within 4 months after the last dose of BI 3810944 Further exclusion criteria apply.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Parte A: Escalada de dosis
|
BI 3810944 |
|
Experimental: Parte B: Expansión de dosis
|
BI 3810944 |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Part A (dose escalation): Occurrence of Cytokine Release Syndrome (CRS) Grade 1 or 2 during the primary Dose Limiting Toxicity (DLT) evaluation period, as a sign of minimal immunological activity that primes the immune system
Periodo de tiempo: approximately 2 months
|
approximately 2 months
|
|
|
Part A (dose escalation): Occurrence of DLTs during the primary DLT evaluation period
Periodo de tiempo: approximately 2 months
|
approximately 2 months
|
|
|
Part B (dose expansion): Objective Response (OR)
Periodo de tiempo: up to 24 months
|
OR, defined as best overall response of confirmed CR and/or confirmed PR, where best overall response is determined according to RECIST v 1.1 assessed from first treatment administration until the earliest event of PD, death or last evaluable tumour assessment during the on-treatment period before start of subsequent anticancer therapy, loss to follow up, withdrawal of consent, or end of trial. |
up to 24 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Parte A (escalada de dosis): Aparición de DLT durante el período de tratamiento
Periodo de tiempo: aproximadamente 2 meses
|
aproximadamente 2 meses
|
|
|
Part A (dose escalation): Occurrence of Adverse Events (AEs) (including SAEs, drug-related AEs, AESIs, and AEs leading to discontinuation of trial drug) during the on-treatment period
Periodo de tiempo: approximately 2 months
|
Serious Adverse Events (SAEs); Adverse Event of Special Interest (AESIs). |
approximately 2 months
|
|
Part B (dose expansion): Occurrence of AEs (including SAEs, drug-related AEs, AESIs, and AEs leading to discontinuation of trial drug) during the on-treatment period
Periodo de tiempo: up to 24 months
|
up to 24 months
|
|
|
Part B (dose expansion): Duration of Response (DoR)
Periodo de tiempo: up to 24 months
|
DoR, defined as the time from first documented Complete Response (CR) or Partial Response (PR) until the earliest of Progressive Disease (PD) or death among trial participants with OR according to RECIST v 1.1. |
up to 24 months
|
|
Part B (dose expansion): Disease Control (DC)
Periodo de tiempo: up to 24 months
|
DC, defined as best overall response of confirmed CR, or confirmed PR, or Stable Disease (SD) where best overall response is defined according to RECIST v 1.1 from first treatment administration until the earliest of PD, death or last evaluable tumour assessment before start of subsequent anticancer therapy, loss to follow-up, withdrawal of consent, or end of trial. |
up to 24 months
|
|
Part B (dose expansion): Progression-Free Survival (PFS)
Periodo de tiempo: up to 24 months
|
PFS, defined as the time from first administration until tumour progression according to RECIST v 1.1 or death from any cause, whichever occurs earlier. |
up to 24 months
|
|
Part A (dose escalation) and Part B (dose expansion): Maximum measured concentration of analytes in serum (Cmax)
Periodo de tiempo: up to 24 months
|
up to 24 months
|
|
|
Part A (dose escalation) and Part B (dose expansion): Area under the serum concentration-time curve over the time interval from 0 to the last measured time point, tz (AUC0-tz)
Periodo de tiempo: up to 24 months
|
up to 24 months
|
|
|
Part A (dose escalation) and Part B (dose expansion): Terminal half-life of analytes (t1/2)
Periodo de tiempo: up to 24 months
|
up to 24 months
|
Colaboradores e Investigadores
Patrocinador
Publicaciones y enlaces útiles
Enlaces Útiles
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
- Neoplasias por tipo histológico
- Enfermedades de la piel
- Tumores neuroectodérmicos
- Neoplasias De Células Germinales Y Embrionarias
- Neoplasias De Tejido Nervioso
- Tumores neuroendocrinos
- Nevos y Melanomas
- Neoplasias De La Piel
- Enfermedades de la piel y del tejido conectivo
- Melanoma
Otros números de identificación del estudio
- 1527-0001
- U1111-1323-2127 (Identificador de registro: WHO International Clinical Trials Registry Platform (ICTRP))
- 2025-522045-21-00 (Identificador de registro: CTIS)
- 2025 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Clinical studies sponsored by Boehringer Ingelheim, phases I to IV, interventional and non-interventional, are in scope for sharing of the raw clinical study data and clinical study documents. Exceptions might apply, e.g. studies in products where Boehringer Ingelheim is not the license holder; studies regarding pharmaceutical formulations and associated analytical methods, and studies pertinent to pharmacokinetics using human biomaterials; studies conducted in a single center or targeting rare diseases (in case of low number of patients and therefore limitations with anonymization).
For more details refer to:
https://www.clinicalstudies.boehringer-ingelheim.com/msw/datasharing
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. .