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NCT06225310 · ClinicalTrials.gov registry record · Phase 1

A Trial of Selinexor, Ruxolitinib and Methylprednisolone

A Phase 1 study of Multiple Myeloma in Relapse and Multiple Myeloma, Refractory, sponsored by Oncotherapeutics.

Recruiting
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT06225310 is a Phase 1 study of Multiple Myeloma in Relapse and Multiple Myeloma, Refractory that is actively recruiting participants, run by Oncotherapeutics. The registered enrollment target is 30 participants, below the 49-participant average among 12 other Multiple Myeloma in Relapse trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06225310, a Phase 1 study of Multiple Myeloma in Relapse and Multiple Myeloma, Refractory, is actively recruiting participants, sponsored by Oncotherapeutics.

RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

Selinexor, a first-in-class, oral selective exportin 1 (XPO1) inhibitor, has shown promise in pre-clinical and clinical studies. It functions by inhibiting the nuclear export protein XPO1, resulting in the accumulation of tumor suppressor proteins and inhibition of oncoprotein mRNAs, which is selectively lethal to myeloma cells. Selinexor has demonstrated activity in combination with various drugs, including glucocorticoids and proteasome inhibitors, leading to its FDA approval for the treatment of relapsed or refractory multiple myeloma.

Interventions

  • DRUG Selinexor
  • DRUG Ruxolitinib
  • DRUG Methylprednisolone

Study Locations (1)

California

  • Berenson Cancer Center - West Hollywood

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2024-08-06
Est. Completion 2027-05-01
Phase Phase 1

Sponsor

Oncotherapeutics

17 total trials

What the Registry Record Tells You About NCT06225310

The ClinicalTrials.gov registry entry for NCT06225310 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 49-participant average among 12 other Multiple Myeloma in Relapse trials with a reported enrollment target (39% lower). The listed sponsor is Oncotherapeutics, which has 17 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Multiple Myeloma in Relapse appearing as the primary indexed condition, and to 3 interventions - of which Selinexor is the first listed.

NCT06225310 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06225310 about?

NCT06225310 is a clinical study titled "A Trial of Selinexor, Ruxolitinib and Methylprednisolone". Selinexor, a first-in-class, oral selective exportin 1 (XPO1) inhibitor, has shown promise in pre-clinical and clinical studies. It functions by inhibiting the nuclear export protein XPO1, resulting in the accumulation of tumor suppressor proteins and inhibition of oncoprotein mRNAs, which is select...

What is the current status of trial NCT06225310?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2024-08-06. Estimated completion is 2027-05-01.

What conditions does trial NCT06225310 study?

This clinical trial studies the following conditions: Multiple Myeloma in Relapse, Multiple Myeloma, Refractory.

What interventions are being tested in trial NCT06225310?

The interventions under investigation include: Selinexor (DRUG), Ruxolitinib (DRUG), Methylprednisolone (DRUG).

Who is sponsoring clinical trial NCT06225310?

This trial is sponsored by Oncotherapeutics, which has 17 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06225310 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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