Autologous Human Adipose-Derived Mesenchymal Stem Cells in Alzheimer's Disease

NCT ID: NCT04855955

Last Updated: 2024-02-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NO_LONGER_AVAILABLE

Study Classification

EXPANDED_ACCESS

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Alzheimer Disease

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Adipose-Derived Mesenchymal Stem Cells

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Celltex Therapeutics Corporation

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Richard L Neel, M.D.

Role: PRINCIPAL_INVESTIGATOR

Little Alsace Urgent Care Center

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CTXSP0001

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Safety and Efficacy of MT-4666
NCT01764243 COMPLETED PHASE2