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Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›GILD›Idelalisib · Bridalveil

Idelalisib · Bridalveil

Efficacy and Safety of Idelalisib (GS-1101) in Combination With Bendamustine and Rituximab for Previously Treated Indolent Non-Hodgkin Lymphomas

Ensayo de GILEAD SCIENCES, INC. en Linfomas no Hodgkin indolentes.

Fase
Fase 3
Estado
Interrumpido
Participantes
475
previstos
Centros
144
Fin del objetivo primario
may 2016
fecha real

Qué significa cada fase y cada estado.

Estudio de intervención, aleatorizado, triple ciego. Comenzó en ene 2013.

Qué mide

Supervivencia libre de progresion (PFS)

Cómo lo describe el promotor

En el documentoEn inglés, del registroThe primary objective of this study is to evaluate the addition of idelalisib to bendamustine/rituximab on progression-free survival (PFS) in adults with previously treated indolent non-Hodgkin lymphoma (iNHL). An increased rate of deaths and serious adverse events (SAEs) among participants with front-line chronic lymphocytic leukemia (CLL) and early-line iNHL treated with idelalisib in combination with standard therapies was observed by the independent data monitoring committee (DMC) during regular review of 3 Gilead Phase 3 studies. Gilead reviewed the unblinded data and terminated this study in agreement with the DMC recommendation and in consultation with the US Food and Drug Administration (FDA).

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Todos los de GILD, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT01732926), actualizada en oct 2018.