Registry of Patients Having Received oNKord®

Recruiting Observational Study
AML
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
50 (estimated)
Sponsor
Glycostem Therapeutics BV · Industry
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About This Trial

ReKORD is an observational study (Registry) enrolling participants who have received at least one dose of oNKord® (allogeneic ex vivo-generated Natural Killer \[NK\] cells from CD34+ umbilical cord blood progenitor cells) in a clinical trial. Participants from multiple previous clinical trials of oNKord® can be enrolled in this Registry.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Receipt of at least one dose of oNKord® in a clinical trial * Participation must be within 3 years after the first infusion of oNKord® * Signature of ICF Exclusion Criteria: * N/A
Contacts

Katarzyna Nowek, PhD

+31(0)412211001

medical@glycostem.com

CONTACT