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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT04855955
Other study ID # CTXSP0001
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information

Verified date February 2024
Source Celltex Therapeutics Corporation
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

This is a single patient emergency expanded access clinical study to assess the safety of administering autologous AdMSCs to an incurable Alzheimer disease patient. The study subject will be evaluated for disease-associated severity according to symptoms, cognitive function, memory, and quality of life.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - The patient is diagnosed with later stage of Alzheimer Disease with sever cognitive disability. - All current anti-Alzheimer medicines cannot prevent disease progression and the patient's mental and physical ability persistently declined - Patient's legal guardian and caregiver must voluntarily sign an approved written consent form after ample explanation of the proposed therapy. Exclusion Criteria: - Current diagnosis of malignancy - Renal/liver dysfunction: Exceed two times as normal subject - Pregnant or nursing - Received other trial drugs within 30 days after participation of this study - Experienced major surgery or trauma in the last 14 days

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Adipose-Derived Mesenchymal Stem Cells


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Celltex Therapeutics Corporation
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