Precision T1D Platform - New Therapies for Cardio-Renal Complications
Accelerating Breakthrough Targeted New Therapies for Cardio-Renal Complications in People With T1D (Precision T1D Platform)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This is a multicenter, open label pilot platform study to evaluate the impact of allocating patients with T1D and early signs of HF/DKD to targeted therapies based on their disease pathway activation signatures. The hypothesis is that stratifying T1D patients by molecularly-defined endophenotypes enables the use of targeted therapies that can more effectively prevent or slow cardio-renal complications.
There is no randomized allocation to treatment arms; rather, the eligible participant's clinical and biomarker data will be reviewed by the Molecular T1D Board which will adjudicate each participant to a treatment arm based on their based on their disease pathway activation signatures. Activation of different treatment arms may be initiated at different time points during the study.
The following sections describe the master protocol, outlining the requirements across all treatment arms, including the study-wide inclusion and exclusion criteria and study-wide procedures. Appendix A outlines any treatment arm/investigational agent specific information, including defining additional treatment-specific eligibility criteria and required study procedures.
The study schema can be found in Section 1.2 and the Schedule of Activities (SoA) in Section 1.3. Potential participants will undergo a two-part consent and screening process. The initial consent and screening visit will be limited to activities necessary for assessment by the Molecular T1D Board. Following review by the Molecular T1D Board, participants will be adjudicated to one treatment arm. At this time, participants will undergo the second consent and screening step, which will include information about specific requirements for their assigned investigational arm and, if in agreement, a complete eligibility assessment via a full screening visit. If the participant is deemed eligible, they will be notified and investigational product will be mailed to them directly. The screening visit results will also serve as the baseline results provided the first dose of study drug is taken within 14 (target) to 21 (limit) days of the screening visit. If more than 21 days, a retest of all laboratory measures will be performed.
Participants will receive open label treatment for 26 weeks, with planned study visits at weeks 2, 6, 12, 26, and 30. The total study duration of participation will be up to 36 weeks, inclusive of the screening period. Active study participation will conclude at Week 30 visit. Following completion of active study participation, participants will enter a passive follow-up period during which the study team may collect information on vital status, survival, hospitalizations, and other relevant clinical outcomes through review of medical records and other authorized data sources for up to 12 months after study participation ended. No additional protocol-required visits, procedures, or interventions will be conducted during the passive follow-up period. Participants will be enrolled in this study at Oregon Health & Science University and the University of Michigan.
The currently planned number of study arms is three, with 15-19 participants enrolled in each arm. The study sponsors will have the option to increase the number of study arms and potential targeted therapies, which would be documented in the appendices and this master protocol.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Laura Nguyen
- Número de teléfono: (971) 509-4222
- Correo electrónico: nguyelau@ohsu.edu
Copia de seguridad de contactos de estudio
- Nombre: Aly Carlson
- Número de teléfono: (971) 610-3005
- Correo electrónico: carlsaly@ohsu.edu
Ubicaciones de estudio
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Michigan
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Ann Arbor, Michigan, Estados Unidos, 48109
- University of Michigan
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Sub-Investigador:
- Matthias Kretzler, MD
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Contacto:
- Hailey Desmond, MS
- Número de teléfono: (734) 764-6955
- Correo electrónico: heturner@med.umich.edu
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Investigador principal:
- Lynn Ang, MD
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Oregon
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Portland, Oregon, Estados Unidos, 97239
- Oregon Health & Science University
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Investigador principal:
- Rodica Busui, MD, PhD
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Sub-Investigador:
- Brian Davidson, MD
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Contacto:
- Laura Nguyen
- Número de teléfono: 971-509-4222
- Correo electrónico: nguyelau@ohsu.edu
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Contacto:
- Aly Carlson
- Número de teléfono: 971-610-3005
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Sub-Investigador:
- Jonathan Purnell, MD
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Sub-Investigador:
- David Ellison, MD
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Sub-Investigador:
- Kristin Childress, MD, MPH
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
Diagnosis of T1D, defined as hyperglycemia requiring treatment with insulin within one year from diagnosis or, if the onset was after age 35 years, documentation of the presence of hyperglycemia and one or more of the following:
- presence of circulating T1D-associated autoantibodies, or
- history of hospitalization for diabetic ketoacidosis, or
- documented plasma C-peptide below the limit of detection with standard assay (with concurrent blood glucose >100 mg/dL)
- Aged 18-75 years, inclusive
- T1D duration >10 years
- HbA1c: 7-10%
Meets one of the following, either
- UACR > 30 mg/dl with eGFR ≥ 60mL/min/1.73 m2 and receiving standard of care therapy for early DKD Stage 2, including renin angiotensin system blockade (RASB), unless contraindicated or not tolerated, or
- Early (Stage B HF) defined as NT-proBNP ≥125 pg/mL
- Willing and able to adhere to schedule of activities and protocol requirements, including written informed consent
Exclusion Criteria:
- Diagnosis of Type 2 diabetes or monogenic forms of diabetes or diabetes secondary to pancreatic disease
- Use of any active platform treatment arms outside study assignment within 2 months prior to screening. See Appendix A for active treatment arms
- Current use of GLP-1 receptor agonists or other non-glucose lowering agent
- Use of aldosterone inhibitors within 2 months prior to screening
- Immunosuppressive medications within 3 months prior to screening
- Systolic BP>160 or diastolic BP >95 mmHg at screening
- History of ≥3 severe hypoglycemic events requiring third-party assistance for correction within 3 months prior to screening
- Evidence of any episode of DKA or non-ketotic hyperosmolar state within 12 months prior to screening
- Serum potassium > 5.0 mmol/L at screening
- Absolute neutrophil count < 2.0 × 109 per L at screening
- Platelet count < 120 × 109 per L at screening
- Known active tuberculosis, hepatitis B or C at screening, or history of HIV
- Current or past history of decompensated cirrhosis (defined as variceal bleeding, ascites or hepatic encephalopathy), and/or known diagnosis of cirrhosis based on liver biopsy, imaging, or elastography, and/or AST or ALT >2 times upper limit of normal, and/or total bilirubin >1.3 times upper limit of normal at screening
- History of severe acquired immune deficiency syndrome or severely immunocompromised status in the opinion of the study site investigator
- History of biopsy-proven non-diabetic CKD
- History of any other cause of HF (viral, congenital, valvular)
- History of heart or renal transplant or currently on chronic dialysis
- Cancer treatment, excluding non-melanoma skin cancer treated by excision, carcinoma in situ of the cervix or uterus, ductal breast cancer in situ, resected non-metastatic breast or prostate cancer, within one year prior to screening
- Illicit drug abuse within 6 months prior to screening in the opinion of the study site investigator
- Current heavy alcohol use (for men, ≥5 drinks on any day or ≥15 drinks per week; for women, ≥4 drinks on any day or ≥8 drinks per week)
- Participation in another interventional clinical research study within 30 days prior to screening
- Breastfeeding, pregnancy, or unwillingness to be on contraception during the trial
- Presence of a clinically significant medical history, physical examination, laboratory finding or other identified study site investigator concern that may interfere with any aspect of study conduct or interpretation of results
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Finerenone
Study participants with biomarker profiles showing a match for finerenone will be adjudicated to this treatment arm.
The clinically recommended dose for finerenone based on manufacturer guidelines is 20 mg once daily (oral) if screening eGFR is ≥60 mL/min/1.73
m2.
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Each treatment arm will be a different unique drug.
There will be no crossing over of participants between arms.
Each participant that is adjudicated to their treatment arm will remain on that arm for the duration of the study through study completion.
Otros nombres:
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|
Experimental: Sotagliflozin
Study participants with biomarker profiles that match with sotagliflozin will be adjudicated to this treatment arm.
The clinically recommended dose of sotagliflozin is 200 mg per the manufacturer guidelines.
The dose of 200 mg has a lower DKA risk and similar kidney benefits to the higher doses.
|
Each treatment arm will be a different unique drug.
There will be no crossing over of participants between arms.
Each participant that is adjudicated to their treatment arm will remain on that arm for the duration of the study through study completion.
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Markers of Renal Health [Safety and Tolerability]
Periodo de tiempo: 26 weeks
|
The primary efficacy endpoints are measures of early (week 26) outcomes on markers of renal health, defined as the percent change from baseline to week 26 in UACR.
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26 weeks
|
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Markes of Cardio Health [Safety and Tolerability]
Periodo de tiempo: 26 weeks
|
The primary efficacy endpoints are measures of early (week 26) outcomes on markers of cardio health as defined by the percent change from baseline to week 26 in NT-proBNP.
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26 weeks
|
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Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Periodo de tiempo: 26 weeks
|
The primary safety endpoints are defined as incidence of serious adverse events, adverse events and clinically significant abnormal laboratory tests.
|
26 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Immediate Outcomes of Renal Health (week 6)
Periodo de tiempo: 20 weeks
|
The secondary endpoints are measures of immediate outcomes on markers of renal health as defined by changes from baseline to week 6 in UACR.
|
20 weeks
|
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Immediate Outcomes of Cardio Health (week 6)
Periodo de tiempo: 20 weeks
|
The secondary endpoints are measures of immediate outcomes on markers of cardio health as defined by changes from baseline to week 6 in NT-proBNP.
|
20 weeks
|
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Immediate (week 6) and Early (week 26) Outcomes of Nephron Function Failure
Periodo de tiempo: 26 weeks
|
The secondary endpoints are measures of immediate outcomes on markers of renal function failure as defined by changes from baseline to week 6 and from baseline to week 26 in eGFR.
|
26 weeks
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Silla de estudio: Rodica Busui, MD, PhD, Oregon Health and Science University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
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
- Enfermedades del sistema endocrino
- Enfermedades cardiovasculares
- Enfermedades cardíacas
- Enfermedades metabólicas
- Enfermedades autoinmunes
- Enfermedades del sistema inmunológico
- Trastornos del metabolismo de la glucosa
- Diabetes mellitus
- Enfermedades Nutricionales y Metabólicas
- Insuficiencia cardiaca
- Diabetes Mellitus, Tipo 1
- (2S,3R,4R,5S,6R)-2-(4-cloro-3-(4-etoxibencil)fenil)-6-(metiltio)tetrahidro-2H-piran-3,4,5-triol
- finerenona
Otros números de identificación del estudio
- 30027
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Marco de tiempo para compartir IPD
Criterios de acceso compartido de IPD
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
- CÓDIGO_ANALÍTICO
- RSC
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.
producto fabricado y exportado desde los EE. UU.
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