Calendario›KPTI›selinexor · KEAP
selinexor · KEAP
Karyopharm Expanded Access Program for Selinexor
Ensayo de Karyopharm Therapeutics Inc. en Multiple Myeloma · Diffuse Large B-Cell Lymphoma (DLBCL) · Sarcoma · Neuroglioblastoma · Peripheral T-cell Lymphoma · Endometrial Cancer · Myelofibrosis · Other (del registro, en inglés).
Más ensayos de: Mieloma múltiple · Sarcoma · Cáncer de endometrio · Mielofibrosis.
Lo que ha anunciado la empresa
La empresa anunció que NO alcanzó su objetivo principal…Phase 3 XPORT-EC-042 trial (NCT05611931), evaluating selinexor as a maintenance-only therapy compared to placebo in adult patients with TP53 wild-type advanced or recurrent endometrial cancer. The trial did not meet its primary endpoint of progression-free survival. A trend favoring the selinexor arm was observed in the modified intent to treat (mITT) population (n=236), with a median PFS of 12.75 months in the selinexor arm compared…
En un 8-K del 13 ago 2026, en una frase que nombra «selinexor». El documento en la SEC.
La empresa anunció que NO alcanzó su objetivo principal…results from its Phase 3 XPORT-EC-042 trial evaluating selinexor as a maintenance-only therapy compared to placebo in adult patients with TP53 wild-type advanced or recurrent endometrial cancer. The trial did not meet its primary endpoint of progression free survival (“PFS”). In the trial, patients were randomized 1:1 to receive either a 60 mg, once-weekly, administration of oral selinexor or placebo until disease progression. The trial…
En un 8-K del 31 jul 2026, en una frase que nombra «selinexor». El documento en la SEC.
La empresa anunció que alcanzó su objetivo principal…results from the Phase 3 SENTRY trial, a randomized, double-blind trial evaluating 60 mg selinexor in combination with ruxolitinib in frontline myelofibrosis compared to ruxolitinib alone (n=353). The trial met the first co-primary endpoint of spleen volume reduction of 35% or more (SVR35) at week 24 and also demonstrated rapid, deep and sustained improvement in this endpoint over time. The trial did not meet its second co-primary endpoint…
En un 8-K del 14 may 2026, en una frase que nombra «selinexor». El documento en la SEC.
- Fase
- no aplica
- Estado
- Disponible por acceso ampliado
Qué significa cada fase y cada estado.
Estudio de acceso ampliado.
Cómo lo describe el promotor
En el documentoEn inglés, del registroKEAP is an expanded access program designed to provide selinexor to eligible participants outside of a clinical trial before the drug has been given marketing approval by the country's regulatory agency or the drug is commercially available in the country. Patients who do not qualify for an ongoing clinical trial but who might benefit from the investigational medicine may be eligible, provided they have exhausted all other available treatment options. Investigational medicines are provided to patients only through treating physicians who obtain the relevant approval on behalf of their patient from the relevant regulatory agency and follow all applicable safety-reporting regulations of the respective country.
Más ensayos de KPTI
| Ensayo | Fase | Estado | Lectura de resultados |
|---|---|---|---|
| Selinexor · SENTRY | Fase 3 | En marcha, sin reclutar | feb 2026 (real) |
| Selinexor · XPORT-EC-042 | Fase 3 | En marcha, sin reclutar | may 2026 (real) |
| Selinexor | Fase 2 | En marcha, sin reclutar | sep 2026 (prevista, ya pasada: sin actualizar en el registro) |
| Selinexor | Fase 2/3 | En marcha, sin reclutar | dic 2026 (prevista) |
| Selinexor | Fase 2 | En marcha, sin reclutar | dic 2026 (prevista) |
| Selinexor · STOMP | Fase 1/2 | Reclutando pacientes | abr 2027 (prevista) |
Todos los de KPTI, en su ficha.
Ficha completa en ClinicalTrials.gov (NCT07215832), actualizada en feb 2026.