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Pierre Fabre anuncia el primer paciente tratado en fase I/II de PFL-002/VERT-002
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Pierre Fabre Laboratories

Oct 24, 2024, 03:15 ET

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-Pierre Fabre anuncia el primer paciente tratado en fase I/II de PFL-002/VERT-002, una terapia dirigida en CPCNP con alteraciones de MET

Pierre Fabre Laboratories anuncia que se ha administrado la primera dosis a un paciente en el ensayo clínico de fase I/II de PFL-002/VERT-002, una innovadora terapia dirigida destinada a tratar el cáncer de pulmón de células no pequeñas con alteraciones de MET

PFL-002/VERT-002 es un anticuerpo monoclonal con un mecanismo de acción novedoso y diferenciado, que actúa como un degradador de c-MET, con el potencial de ser el mejor tratamiento de su clase para el cáncer provocado por alteraciones de MET

CASTRES, Francia, 24 de octubre de 2024 /PRNewswire/ -- Pierre Fabre Laboratories anunció hoy que el primer paciente ha recibido una dosis de PFL-002/VERT-002, un anticuerpo monoclonal que actúa como degradador de c-MET, en un ensayo de fase I/II de aumento de dosis, optimización de dosis y expansión de dosis, para pacientes con cáncer de pulmón de células no pequeñas (CPCNP) que albergan alteraciones de MET.

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Pierre Fabre Laboratories Announce First Patient Dosed in Phase I/II Clinical Trial of PFL-002/VERT-002, an Innovative Targeted Therapy Intended to Treat NonSmall Cell Lung Cancer with MET Alterations
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Pierre Fabre Laboratories Announce First Patient Dosed in Phase I/II Clinical Trial of PFL-002/VERT-002, an Innovative Targeted Therapy Intended to Treat NonSmall Cell Lung Cancer with MET Alterations

El ensayo de fase I/II PFL-002/VERT-002 es un estudio multicéntrico abierto que tiene como objetivo evaluar la seguridad, tolerabilidad, farmacocinética, farmacodinámica y eficacia clínica preliminar de PFL-002/VERT-002, como monoterapia para pacientes con tumores dependientes de MET, incluidos aquellos que presentan resistencia adquirida a otros tratamientos.

El cáncer de pulmón de células no pequeñas (CPCNP) es la forma más prevalente de cáncer de pulmón, representando aproximadamente el 85% de los casos de cáncer de pulmón diagnosticados recientemente, y MET, también conocido como receptor del factor de crecimiento de hepatocitos (HGFR), es un oncogén impulsor en subgrupos de pacientes que padecen CPCNP.1-4 La mutación de omisión del exón 14 de MET y la amplificación de MET se encuentran como impulsores oncogénicos primarios y la amplificación de MET como un mecanismo de resistencia a terapias dirigidas seleccionadas.

"PFL-002/VERT-002 actúa sobre un promotor oncogénico clínicamente validado con un mecanismo de acción único y diferenciado, que desencadena la degradación del oncogén c-MET. Por lo tanto, ofrece la oportunidad de probar un nuevo enfoque terapéutico para pacientes con tumores impulsados por MET. Esperamos colaborar con los investigadores que participan en el primer ensayo en humanos para evaluar la seguridad y eficacia de este nuevo agente", afirmó Francesco Hofmann, director de Investigación y Desarrollo para Atención Médica en Pierre Fabre Laboratories.

Contacto: [email protected] 

PDF - https://mma.prnewswire.com/media/2538658/Pierre_Fabre_PFL_002_Vert_002.pdf
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