Study of KPT-330 (Selinexor) in Female Patients With Advanced Gynaecologic Malignancies

PHASE2CompletedINTERVENTIONAL
Enrollment

116

Participants

Timeline

Start Date

April 9, 2014

Primary Completion Date

January 24, 2017

Study Completion Date

March 29, 2017

Conditions
Ovarian CarcinomaEndometrial CarcinomaCervical Carcinoma
Interventions
DRUG

Selinexor

"Route of administration and dosage form: Oral tablet; Doses: 35 mg/m\^2 BIW, 35 mg/m\^2 QW, 50 mg/m\^2 BIW, 50 mg/m\^2 QW, 60 mg/m\^2 BIW, 60 mg/m\^2 QW.~Treatment cycles were 4 weeks each i.e., 28 day cycles."

Trial Locations (4)

B-3000

UZ Leuven - Universitair Ziekenhuis Leuven, Leuven

DK-9100

Aalborg University Hospital, Aalborg

DK-2100

Rigshospitalet, Copenhagen

DK-2730

Herlev Hospital, Herlev

Sponsors
All Listed Sponsors
lead

Karyopharm Therapeutics Inc

INDUSTRY

NCT02025985 - Study of KPT-330 (Selinexor) in Female Patients With Advanced Gynaecologic Malignancies | Biotech Hunter | Biotech Hunter