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CAR T-cell Therapy
Study Evaluating Safety and Efficacy of UCART Targeting CS1 in Patients With Relapsed/Refractory Multiple Myeloma (MELANI-01)
Phase 1
Waitlist Available
Research Sponsored by Cellectis S.A.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new treatment called UCARTCS1A, which uses modified immune cells to target and kill cancer cells. It is aimed at patients with multiple myeloma that has come back or didn't respond to other treatments. The goal is to see if this treatment is safe and effective. UCARTCS1A is a type of CAR-T cell therapy, which is a promising approach in treating multiple myeloma by using modified immune cells to target cancer cells.
Eligible Conditions
- Relapsed or Refractory Multiple Myeloma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety of UCARTCS1A
Secondary study objectives
Duration of Response
Overall Survival
Progression Free Survival
+1 moreAwards & 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: Dose EscalationExperimental Treatment1 Intervention
Several tested doses of UCARTCS1A until the Maximum Tolerated Dose (MTD) is identified.
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Who is running the clinical trial?
Cellectis S.A.Lead Sponsor
5 Previous Clinical Trials
186 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have not been treated before with experimental gene targeting CS1 or chimeric antigen receptor therapy targeting CS1.
Research Study Groups:
This trial has the following groups:- Group 1: Dose Escalation
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.