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Human Umbilical Cord Mesenchymal Stem Cells

Generic Name
Human Umbilical Cord Mesenchymal Stem Cells
Drug Type
Biotech

Overview

Stem cells obtained from amniotic fluid, the umbilical cord (UC), and placenta are gaining in popularity. Stem cells from the umbilical cord offer several advantages, including: non-invasive collection procedures, more hearty and steady growth than bone-marrow derived stem cells (they can maintain a steady doubling time (DT) over up to 10 passages), higher differentiation capability, and faster self-renewal. These cells express low levels of major histo-compability complex (MHC) class I, and generally lack MHC class II and its co-stimulatory ligands like CD40, CD80, and CD86. Thus, they are characterized with low immunogenicity. The umbilical cord, which starts developing in the fifth week of gestation, contains different compartments where stem cells originate: the cord lining, Wharton’s jelly, and perivascular region. UC mesenchymal cells derived from Wharton’s jelly are the most studied and offer more stable and better osteogenic and adipogenic differentiation potentials. The cells are extracted by either the explant or the enzymatic digestion method, though neither method has been characterized as the ‘standard’ thus far. The explant method requires manual mincing of the tissue fragments and results in an inconsistent number of extracted MSCs. In contrast, the enzymatic digestion method uses enzymes to break down the non-required cell fragments, and results in more consistent cell numbers. Regardless of extraction method, the cells are usually expanded in vitro in laboratories using culture systems and bioreactors. The cord lining of the UC is generally isolated with the explant method -- resulting in two kinds of MSCs: cord lining mesenchymal stem cells (CLMC), which are used to aid in burn and diabetic ulcer wound healing, and cord lining epithelial stem cells (CLEC), which are used for persistent corneal epithelial defects and skin improvements. Currently many companies are creating their own version of these stem cells, one of which is by Aspire, who are creating a version named ACT-20.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/02/06
Phase 1
Completed
2024/12/27
Not Applicable
Recruiting
2024/12/04
Phase 3
Recruiting
Shanghai IxCell Biotechnology Co., LTD
2024/11/20
Not Applicable
Active, not recruiting
2024/06/18
Phase 1
Recruiting
Wuhan Union Hospital, China
2023/01/30
Phase 2
Recruiting
2022/03/18
Phase 1
Withdrawn
2022/02/04
Phase 2
Recruiting
Beijing 302 Hospital
2021/05/05
Phase 1
Completed
2020/09/24
Not Applicable
UNKNOWN

FDA Drug Approvals

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No FDA approvals found for this drug.

EMA Drug Approvals

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No EMA approvals found for this drug.

HSA Drug Approvals

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No HSA approvals found for this drug.

NMPA Drug Approvals

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No NMPA approvals found for this drug.

PPB Drug Approvals

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No PPB approvals found for this drug.

TGA Drug Approvals

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No TGA approvals found for this drug.

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