Trials / Recruiting
RecruitingNCT05530421
Selinexor, Venetoclax, and Dexamethasone (XVenD) in t(11;14)-Positive Relapsed/Refractory Multiple Myeloma
Selinexor, Venetoclax, and Dexamethasone (XVenD) in t(11;14)-Positive Relapsed/Refractory Multiple Myeloma (SELVEDge Study)
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 33 (estimated)
- Sponsor
- University of Miami · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this research is to determine whether the combination of selinexor, venetoclax, and dexamethasone therapy can increase anti-cancer effects in patients with translocation 11;14-positive (t(11;14)), relapsed/refractory myeloma (RRMM).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Selinexor | Selinexor tablets will be administered orally (PO) once per day at assigned dosage and frequency per protocol. |
| DRUG | Venetoclax | Venetoclax tablets will be administered orally (PO) once per day at assigned dosage and frequency per protocol. |
| DRUG | Dexamethasone | Dexamethasone tablets will be administered orally (PO) once per day at assigned dosage and frequency per protocol. |
Timeline
- Start date
- 2023-03-26
- Primary completion
- 2028-03-26
- Completion
- 2030-03-26
- First posted
- 2022-09-07
- Last updated
- 2026-02-23
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05530421. Inclusion in this directory is not an endorsement.