E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Hepatocellular carcinoma or other solid tumors characterized by positive FGFR4 and KLB expression |
Carcinoma hepatocelular u otros tumores sólidos caracterizados por la expresión positiva de FGFR4 y KLB |
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E.1.1.1 | Medical condition in easily understood language |
Hepatocellular carcinoma (liver cancer) or other types of cancer. |
carcinoma hepatocelular (cáncer de hígado) u otros tipos de cáncer. |
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E.1.1.2 | Therapeutic area | Diseases [C] - Cancer [C04] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 17.0 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10065252 |
E.1.2 | Term | Solid tumor |
E.1.2 | System Organ Class | 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
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E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 17.0 |
E.1.2 | Level | PT |
E.1.2 | Classification code | 10073071 |
E.1.2 | Term | Hepatocellular carcinoma |
E.1.2 | System Organ Class | 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
1. Phase I part: to estimate the MTD and/or RP2D of FGF401 2. Phase II part: to investigate the anti-tumor activity of FGF401 |
Fase I: Estimar la DMT o la DRF2 de FGF401. Fase II: Investigar la actividad antitumoral de FGF401. |
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E.2.2 | Secondary objectives of the trial |
1. To characterize the safety and tolerability of FGF401 2. To further investigate the anti-tumor activity of FGF401 3. To characterize the PK properties of FGF401 |
1. Caracterizar la seguridad y la tolerabilidad de FGF401. 2. Continuar investigando la actividad antitumoral de FGF401. 3. Caracterizar las propiedades PK de FGF401, 4. Evaluar el efecto de los alimentos en la exposición a FGF401 y el perfil de seguridad. |
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
1. Patients (male or female) ? 18 years of age 2. ECOG Performance Status ? 1 3. Presence of at least one measurable lesion according to RECIST v1.1. 4. Patients with confirmed positive expression of FGFR4 and KLB at pre-screening. 5. For HCC patients: the diagnosis must be made based on AASLD Guidelines with confirmed stage C advanced HCC (BCLC staging classification). Current cirrhotic status of Child-Pugh class A (5-6 points), with no encephalopathy and/or ascites. 6. Phase I: Patients with HCC or advanced solid tumors, who have progressed despite standard therapy or are intolerant of standard therapy, or for whom no standard therapy exists. 7. Phase 2: HCC patients previously treated with sorafenib for advanced HCC with documented disease progression during or after discontinuation of sorafenib treatment, or intolerance to sorafenib treatment.
Other protocol-defined inclusion criteria may apply. |
1. Pacientes (hombres o mujeres) ? 18 años de edad. 2. Estado funcional ECOG ? 1. 3. Presencia de al menos una lesión medible según RECIST v1.1. 4. Pacientes con expresión positiva confirmada de FGFR4 y KLB en la preselección. 5. Pacientes con CHC: el diagnóstico debe realizarse basándose en las Directrices de la AASLD con CHC avanzado de estadio C confirmado (clasificación de estadios del BCLC). Estado cirrótico actual de clase A de Child-Pugh (5-6 puntos) sin encefalopatía ni ascitis. 6. Fase I y fase II, grupo 3: Pacientes con CHC o tumores sólidos avanzados que hayan progresado a pesar del tratamiento estándar o que no toleren el tratamiento estándar o para quienes no exista tratamiento estándar. 7. Fase II, grupos 1 y 2: Pacientes con CHC previamente tratados con sorafenib para CHC avanzado con progresión de la enfermedad documentada durante o después de la retirada del tratamiento con sorafenib o intolerancia al tratamiento con sorafenib. |
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E.4 | Principal exclusion criteria |
1. Previous treatment with a FGF19-FGFR4 targeting therapy. 2. For HCC patients in Phase II part: any previous systemic anti-cancer therapies other than sorafenib or any anti-cancer therapy (including locoregional therapy) after disease progression during or after sorafenib treatment. 3. Ongoing active diarrhea requiring medications (e.g. BAS, loperamide) 4. Irritable bowel syndrome with signs/symptoms and requires medications 5. Symptomatic CNS metastases which are neurologically unstable or requiring increasing doses of steroids to control their CNS disease. 6. Patient having out of range laboratory values defined as: ? Hematology Hemoglobin ? 9 g/dL (SI Units: 90 g/L) Platelet count < 75000/mm3 Absolute neutrophil count (ANC) < 1500/mm3 ? Chemistry Total bilirubin ? 2 mg/dL AST and/or ALT > 3 x ULN Serum creatinine > 1.5 x ULN and/or creatinine clearance ? 45 mL/min ? Coagulation: PT ? 4 seconds or INR ? 1.7 7. Unable to stop any prohibited medications, including CYP1A2, CYP2C9 and CYP3A substrates with a narrow therapeutic index, long acting proton pump inhibitors, and strong BSEP efflux transporter inhibitors.
Other protocol-defined exclusion criteria may apply. |
1. Tratamiento previo con un tratamiento dirigido a FGF19-FGFR4 selectivo y/o un inhibidor pan-FGFR. 2. Para pacientes con CHC en la fase II: cualquier tratamiento anticancerígeno sistémico previo, salvo sorafenib o cualquier tratamiento anticancerígeno (incluido el tratamiento locorregional) después de la progresión de la enfermedad durante o después del tratamiento con sorafenib. 3. Diarrea activa en curso que requiera medicación (p. ej., SAB, loperamida). 4. Síndrome del intestino irritable con signos/síntomas y que requiera medicación. 5. Metástasis del SNC sintomáticas que sean neurológicamente inestables o que requieran un aumento de las dosis de esteroides para controlar la enfermedad del SNC. |
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E.5 End points |
E.5.1 | Primary end point(s) |
1. Incidence rate and characteristics of DLT during the first cycle of dosing 2. Group 1 and Group 2: Time to progression (TTP); Group 3: Overall response rate (ORR), based on local assessment per RECIST v1.1 |
1. tasa de incidencia y características de DLT durante el primer ciclo de dosificación 2. Grupo 1 y Grupo 2: tiempo hasta la progresión (TTP); Grupo 3: Tasa de respuesta global (ORR), basado en la evaluación local por RECIST v1.1 |
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E.5.1.1 | Timepoint(s) of evaluation of this end point |
1. First cycle 2. Baseline and every 6 weeks |
1. Primer ciclo 2. basal y cada 6 semanas |
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E.5.2 | Secondary end point(s) |
1. Safety: Incidence and severity of AEs and SAEs, including changes in laboratory values, vital signs and ECGs Tolerability: Dose interruptions and reductions
2. Phase I part: BOR, ORR, DCR, TTP and OS, based on local assessment per RECIST v1.1 Phase II part: ? Group 1 and Group 2: BOR, ORR, OS and DCR, based on local assessment per RECIST v1.1 ? Group 3: BOR, DCR, OS and PFS, based on local assessment per RECIST v1.1
3. Plasma concentration of FGF401 and PK parameters including but not limited to Cmax, Cmin, AUCinf, AUClast, AUCtau and T1/2 |
1. Seguridad: La incidencia y severidad de acontecimientos adversos y acontecimientos adversos graves, incluidos los cambios en los valores de laboratorio, signos vitales y ECG Tolerabilidad: interrupciones y reducciones de dosis 2. Fase I parte: BOR, la ORR, DCR, TTP y OS, basado en la evaluación local por RECIST v1.1 Fase II parte: ? Grupo 1 y Grupo 2: BOR, la ORR, OS y DCR, basado en la evaluación local por RECIST v1.1 ? Grupo 3: BOR, DCR, SG y SLP, basado en la evaluación local por RECIST v1.1 3. concentración de plasma de los parámetros de PK y FGF401 incluyendo pero no limitado a Cmax, Cmin, AUCinf, AUCúlt, AUCtau y T1 / 2 |
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E.5.2.1 | Timepoint(s) of evaluation of this end point |
1. Continuously throughout the study until 30 days after safety follow up 2. Baseline and every 6 weeks 3. During phase I: Cycle 1 Day 1, 2, 8, 9 and 15; Cycle 2 Day 1 and 2; Cycle 3 and Cycle 4 Day 1 During Phase II: Cycle 1 Day 1, 2, 8 and 15; Cycle 2 Day 1 and 2; Cycle 3 to Cycle 6 Day 1 |
1. Continuamente durante todo el estudio hasta el 30 días después de la seguridad de seguimiento 2. basal y cada 6 semanas 3. Durante la fase I: Ciclo 1 Día 1, 2, 8, 9 y 15; Ciclo 2 Día 1 y 2; Ciclo 3 Ciclo 4 y Día 1 Durante la Fase II: Ciclo 1 Día 1, 2, 8 y 15; Ciclo 2 Día 1 y 2; Ciclo 3 a 6 Ciclo Día 1 |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | Yes |
E.7.1.1 | First administration to humans | Yes |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | Yes |
E.7.3 | Therapeutic confirmatory (Phase III) | No |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | No |
E.8.1.1 | Randomised | No |
E.8.1.2 | Open | Yes |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | No |
E.8.1.5 | Parallel group | No |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | No |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| Yes |
E.8.4 | The trial involves multiple sites in the Member State concerned | No |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 12 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | No |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
China |
France |
Germany |
Hong Kong |
Italy |
Japan |
Korea, Republic of |
Singapore |
Spain |
Taiwan |
United States |
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E.8.7 | Trial has a data monitoring committee | No |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
|
The study will end when the treatment period, safety follow-up, disease follow-up and survival follow-up have been completed for all patients, or when the study is terminated early. Completion of the survival follow-up period will occur once a minimum of 80% of patients in the phase II part have died, have been lost to follow-up, or have been followed for survival for 10 months after the last dose of study treatment. |
El estudio finaliza cuando se complete en los pacientes el periodo de tratamiento,seguimiento de seguridad,seguimiento de enfermedad y seguimiento de supervivencia o cuando finalice el estudio prematuramente. El fin del periodo de seguimiento de supervivencia tendrá lugar cuando un mínimo de un 80% de pacientes en la fase II haya fallecido, sea pérdida de seguimiento o se le realice un seguimiento de supervivencia durante 10meses después de la última dosis del tratamiento del estudio |
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 1 |
E.8.9.1 | In the Member State concerned months | 8 |
E.8.9.1 | In the Member State concerned days | 21 |
E.8.9.2 | In all countries concerned by the trial years | 1 |
E.8.9.2 | In all countries concerned by the trial months | 8 |
E.8.9.2 | In all countries concerned by the trial days | 21 |