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Stem Cell Transplant
Cord Blood Transplant for Blood Disorders
Phase 2
Recruiting
Led By Richard W Childs, M.D.
Research Sponsored by National Heart, Lung, and Blood Institute (NHLBI)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must not have
Patients who are receiving licensed CB products (only)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year post transplant
Awards & highlights
No Placebo-Only Group
Summary
This trial will test the safety of unlicensed cord blood units in people who need stem cell transplants.
Who is the study for?
This trial is for individuals of any age and gender who need a stem cell transplant due to conditions like leukemia, lymphoma, or anemia. They must be part of another clinical trial for the transplant and give informed consent. Those already receiving unlicensed cord blood from other banks or licensed products only cannot participate.
What is being tested?
The study tests the safety and effectiveness of unlicensed cord blood units used in stem cell transplants. Participants will receive these units during their standard transplant procedure and will be monitored for up to one year for any issues.
What are the potential side effects?
Potential side effects are related to stem cell transplantation procedures which may include infection risk, graft-versus-host disease (where transplanted cells attack your body), bleeding complications, organ damage, and reactions to the infusion.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently using approved cannabinoid-based products.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year post transplant
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year post transplant
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Cone-Rod Dystrophy 2
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: 1Experimental Treatment1 Intervention
at least one
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Who is running the clinical trial?
National Heart, Lung, and Blood Institute (NHLBI)Lead Sponsor
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am eligible for a stem cell transplant trial using cord blood.I am currently using approved cannabinoid-based products.You are currently receiving unapproved cord blood products from sources other than the study.
Research Study Groups:
This trial has the following groups:- Group 1: 1
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.
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