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Trials / Active Not Recruiting

Active Not RecruitingNCT05954780

Selinexor (Nexpovio®) (SVd) in Patients With Relapsed or Refractory Multiple Myeloma

A Non-interventional Study of Selinexor (Nexpovio®) in Combination With Bortezomib and Dexamethasone (SVd) in Patients With Relapsed or Refractory Multiple Myeloma (R/RMM)

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
75 (actual)
Sponsor
iOMEDICO AG · Industry
Sex
All
Age
18 Years
Healthy volunteers

Summary

The non-interventional study SEATTLE aims to answer open scientific questions regarding QoL and tolerability/safety and AE management of selinexor as well as effectiveness and dosing in clinical routine. Thus, SEATTLE will provide real-world evidence complementary to pivotal studies.

Detailed description

Multiple myeloma (MM) accounts for approximately 10% of hematological malignancies. Since MM patients are elderly and often comorbid patients, risk-adapted treatment strategies to further improve outcome in is crucial.Selinexor, a potent, oral, SINE (selective inhibitors of nuclear exports) binds reversibly to XPO. This leads to nuclear localization and functional activation of tumor suppressor proteins, which further leads to suppression of nuclear factor κB activity, and reduction in oncoprotein mRNA translation. All this induces apoptosis of tumor cells. Since treatment options for MM are various and the most important factor is to keep or improve quality of life (QoL) of the patients, there is an urge for real-world clinical data of MM patients treated with selinexor in clinical routine. The objective of this non-interventional study is to evaluate QoL and tolerability/safety and AE management as well as effectiveness and dosing in adult patients with relapsed or refractory MM, which receive selinexor in combination with bortezomib and dexamethasone in the 2nd or later therapy line in a real-world setting.

Conditions

Interventions

TypeNameDescription
DRUGSelinexorSelinexor/bortezomib/dexamethasone according to Nexpovio® SmPC

Timeline

Start date
2023-06-28
Primary completion
2026-10-30
Completion
2026-10-30
First posted
2023-07-20
Last updated
2026-01-14

Locations

2 sites across 2 countries: Austria, Germany

Source: ClinicalTrials.gov record NCT05954780. Inclusion in this directory is not an endorsement.