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CK2 Inhibitor

CX-4945 for Multiple Myeloma

Phase 1
Waitlist Available
Research Sponsored by Cylene Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one year - assessed throughout all cycles of participation
Awards & highlights
No Placebo-Only Group

Summary

This Phase 1 study of oral CX-4945 is designed to test the safety, tolerability, and highest safe dose level of this CK2 inhibitor in patients with relapsed or refractory multiple myeloma.

Eligible Conditions
  • Multiple Myeloma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one year (assessed at cycle 1).
This trial's timeline: 3 weeks for screening, Varies for treatment, and one year (assessed at cycle 1). for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Safety
Secondary study objectives
Assess for efficacy response
Pharmacokinetic and pharmacodynamic assessments.

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: CX-4945Experimental Treatment1 Intervention
CX-4945 oral formulation
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Silmitasertib
Not yet FDA approved

Find a Location

Who is running the clinical trial?

Cylene PharmaceuticalsLead Sponsor
5 Previous Clinical Trials
165 Total Patients Enrolled
1 Trials studying Multiple Myeloma
55 Patients Enrolled for Multiple Myeloma
Study DirectorStudy DirectorCylene Pharmaceuticals
1,271 Previous Clinical Trials
503,902 Total Patients Enrolled
25 Trials studying Multiple Myeloma
4,738 Patients Enrolled for Multiple Myeloma
~1 spots leftby Nov 2025
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