MADRID, 1 Feb. (EUROPA PRESS) -
Inyectar cantidades diminutas de dos agentes inmunoestimulantes directamente en tumores sólidos en ratones puede eliminar todos los rastros de cáncer en los animales, incluidas las metástasis distantes y no tratadas, según un estudio realizado por investigadores de la Facultad de Medicina de la Universidad de Stanford, en Palo Alto, California, Estados Unidos. El enfoque funciona para muchos tipos diferentes de cánceres, incluidos los que surgen espontáneamente, según el estudio.
Los científicos creen que la aplicación local de cantidades muy pequeñas de los agentes podría servir como una terapia contra el cáncer rápida y relativamente barata que es poco probable que cause los efectos secundarios adversos que a menudo se observan con la estimulación inmune en todo el cuerpo.
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01 febrero 2018
Sylentis // Tivanisiran ( SYL1001 ) /// Actualización Fase III . Estimated Primary Completion Date : March 2018 .
HELIX, a Double-masked Study of SYL1001 in Patients With Moderate to Severe Dry Eye ).
View of NCT03108664 on 2018_01_24
ClinicalTrials Identifier: NCT03108664
Updated: 2018_01_24
Brief Summary:
The purpose of this study is to determine whether SYL1001 ophthalmic solution is safe and effective in the treatment of signs and symptoms of Dry Eye Disease.
Study Design
Study Type : Interventional (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: HELIX, a Double-masked Study of SYL1001 in Patients With Moderate to Severe Dry Eye
Actual Study Start Date : May 18, 2017 .
Estimated Primary Completion Date :
March 2018 ( Anticipated ).
Estimated Study Completion Date :
December 2018 ( Anticipated ).
View of NCT03108664 on 2018_01_24
ClinicalTrials Identifier: NCT03108664
Updated: 2018_01_24
Brief Summary:
The purpose of this study is to determine whether SYL1001 ophthalmic solution is safe and effective in the treatment of signs and symptoms of Dry Eye Disease.
Study Design
Study Type : Interventional (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: HELIX, a Double-masked Study of SYL1001 in Patients With Moderate to Severe Dry Eye
Actual Study Start Date : May 18, 2017 .
Estimated Primary Completion Date :
March 2018 ( Anticipated ).
Estimated Study Completion Date :
December 2018 ( Anticipated ).