NCT06452446Active, not recruiting
Telehealth-based Symptom Management for Veterans Treated With Selinexor
Source: ClinicalTrials.gov · Last updated 10 Feb 2025
Brief summary (registry, in English)
The purpose of this study is to find out if continued monitoring of side effects from Selinexor and prescribed medication to prevent side effects helps improve symptoms, quality of life, and ability to continue the treatment longer.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 20 (estimated)
- First submitted
- 5 Jun 2024
- Start date
- 1 Sept 2024
- Primary completion date
- 1 Jul 2026
- Lead sponsor
- Durham VA Medical Center
- Diseases
- Multiple myeloma
- NCT number
- NCT06452446
What you commit to
- Study type: Observational
- Planned participants: 20
- From 1 Sept 2024 to the primary completion date, 1 Jul 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Any prior or current therapy with selinexor.
- Current selinexor therapy that is part of an investigational clinical trial.
Other illness
- Any medical, psychiatric, or cognitive issue that the principal investigator or the subject's oncologists believes would prevent participation or completion of the study.
Other
- Individuals who are vulnerable to coercion or undue influence.
- Any individuals or populations that may temporarily or permanently require additional considerations include such as those susceptible to coercion or undue influence (e.g., patients with limited or no treatment options, socially and economically disadvantaged persons).
Who the study is looking for
- Diagnosis of B-cell malignancy: either relapsed or refractory multiple myeloma or diffuse large B-cell lymphoma, meeting the FDA-approved indication for Selinexor treatment.
- Requiring therapy as assessed by the treating oncology provider.
- Prior authorization drug request for selinexor approved by VA oncology pharmacist.
- Subject age 18 years or older.
- Subject willing and able to perform video or telephone research visits.
- Subjects must be able to read and comprehend English.
- Subject must be a Veteran receiving cancer care from a VA facility affiliated with the National Teleoncology Program.
- Patients must be enrolled prior to starting Selinexor.
Age in the registry: 18 years to 89 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Durham VA Medical Center Coordinator of this site? Confirm its status | Durham | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.