NCT07215832

Brief Summary

KEAP 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.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 30, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

October 14, 2025

Completed
Last Updated

March 2, 2026

Status Verified

February 1, 2026

First QC Date

September 30, 2025

Last Update Submit

February 26, 2026

Conditions

Keywords

selinexor

Interventions

KPT-330

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Multiple MyelomaLymphoma, Large B-Cell, DiffuseSarcomaLymphoma, T-Cell, PeripheralEndometrial NeoplasmsPrimary Myelofibrosis

Interventions

selinexor

Condition Hierarchy (Ancestors)

Neoplasms, Plasma CellNeoplasms by Histologic TypeNeoplasmsHemostatic DisordersVascular DiseasesCardiovascular DiseasesParaproteinemiasBlood Protein DisordersHematologic DiseasesHemic and Lymphatic DiseasesHemorrhagic DisordersLymphoproliferative DisordersImmunoproliferative DisordersImmune System DiseasesLymphoma, B-CellLymphoma, Non-HodgkinLymphomaLymphatic DiseasesNeoplasms, Connective and Soft TissueLymphoma, T-CellUterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesMyeloproliferative DisordersBone Marrow Diseases

Central Study Contacts

Karyopharm Medical Information

CONTACT

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 30, 2025

First Posted

October 14, 2025

Last Updated

March 2, 2026

Record last verified: 2026-02