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Emmaus Life Sciences presentará ensayos clínicos de anemia drepanocítica de fase 3 en la 56a. Reunión Anual de la Sociedad Estadounidense de Hematología
  • USA - English

Se destaca en el resumen: reducción en la frecuencia de crisis de anemia drepanocítica, frecuencia en las hospitalizaciones, días de hospital y menos casos de síndrome torácico agudo

La presentación oral está programada para el 7 de diciembre de 2014


News provided by

Emmaus Life Sciences, Inc.

Nov 24, 2014, 04:53 ET

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TORRANCE, California, 24 de noviembre de 2014 /PRNewswire/ -- Emmaus Life Sciences, Inc. (la "Compañía" o "Emmaus"), anunció hoy que el Dr. Yutaka Niihara, M.D., M.P.H., fundador y CEO de Emmaus, presentará los resultados del ensayo clínico de la Compañía, de fase 3, de su tratamiento oral de grado farmacéutico L-glutamina (PGLG) para anemia drepanocítica y beta-0 talasemia, en una presentación oral el domingo 7 de diciembre de 2014 a las 4:45 p.m. PST, durante la  56a. Reunión Anual de la Sociedad Estadounidense de Hematología (American Society of Hematology, ASH). La conferencia se realizará los días 6 al 9 de diciembre de 2014 en San Francisco, California, en el Marriott Marquis.

"Nos complace participar en la reunión de la ASH para presentar los resultados positivos en cuanto a seguridad y eficacia de nuestro ensayo de fase 3 de PGLG para el tratamiento de pacientes con anemia drepanocítica", dijo el Dr. Niihara. "Creemos que los resultados demuestran un perfil de seguridad de buena tolerancia que tiene el potencial de ayudar a pacientes adultos y pediátricos que necesiten nuevas terapias a tratar esta enfermedad".

El Dr. Niihara presentará los datos del ensayo clínico prospectivo, randomizado, doble ciego, controlado con placebo, de grupos paralelos, multicéntrico, que incluyó a 230 pacientes adultos y pediátricos, incluso de cinco años de edad, en  31 lugares en EE. UU. Los beneficios clínicos del tratamiento PGLG, como se informa en el resumen, incluyen una reducción en la frecuencia media de crisis de anemia drepanocítica, una frecuencia media más baja de hospitalizaciones, una reducción en la media acumulativa de días de hospital, y menos casos de síndrome torácico agudo, con un perfil de seguridad de buena tolerancia.

Detalles de la presentación oral:

Cuándo: domingo 7 de diciembre de 2014 a las 4:45 p.m. PST

Lugar: Golden Gate Hall (San Francisco Marriott Marquis)

Título de la sesión: Estudio de fase 3 de terapia de L-Glutamina para anemia drepanocítica y beta-0-talasemia

Número de la sesión en el resumen: 86

El resumen está disponible en el sitio web de la ASH o se puede visitar en https://ash.confex.com/ash/2014/webprogram/Paper70720.html

La investigación de la Compañía sobre anemia drepanocítica y beta-0-talasemia fue iniciada por el Dr. Niihara en el Los Angeles Biomedical Research Institute del Harbor-UCLA Medical Center. La terapia está designada como medicamento sin interés comercial en EE. UU. y Europa, y de trámite rápido  según la FDA.

Acerca de Emmaus Life Sciences

Emmaus Life Sciences está dedicada al descubrimiento, desarrollo y comercialización de terapias y tratamientos innovadores para enfermedades raras.

Si desea más información, sírvase visitar www.emmauslifesciences.com.

Declaraciones a futuro

Este comunicado de prensa contiene declaraciones a futuro tal como ese término está definido en la Ley de Reforma de Litigios de Títulos Valores de 1995, en relación con la investigación, el desarrollo y la potencial comercialización de productos farmacéuticos. Tales declaraciones a futuro se basan en expectativas actuales e implican riesgos e incertidumbres inherentes, incluso factores que pudieran retrasar, desviar o cambiar cualquiera de estas, y que pudieran determinar que los resultados reales difirieran sustancialmente de las expectativas actuales. Riesgos e incertidumbres adicionales se describen en los informes presentados por Emmaus Life Sciences, Inc. ante la Comisión de Bolsa y Valores de Estados Unidos, incluso su Informe Anual en el Formulario 10-K para el año que cerró el 31 de diciembre de 2013 y los Informes Trimestrales en el Formulario 10-Q. Emmaus brinda esta información efectiva a la fecha de este comunicado de prensa y no asume ninguna obligación de actualizar ninguna de las declaraciones a futuro como resultado de nueva información, eventos futuros u otras razones.

Contactos:

Medios: 
Lori Teranishi para Emmaus Life Sciences, Inc. 
510-290-6160 
[email protected]

Inversores: 
Matt Sheldon para Emmaus Life Sciences, Inc. 
310-279-5975 
[email protected]

FUENTE Emmaus Life Sciences, Inc.

Related Links

http://www.emmauslifesciences.com

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