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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
Study 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 weeks3 visits
Treatment ~ Varies
Follow Up ~ one year (assessed at cycle 1).
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one year (assessed at cycle 1).
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Safety
Secondary outcome measures
Assess for efficacy response
Establish the recommended Phase 2 dose
Pharmacokinetic and pharmacodynamic assessments.
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
1,214 Previous Clinical Trials
499,492 Total Patients Enrolled
25 Trials studying Multiple Myeloma
7,508 Patients Enrolled for Multiple Myeloma
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