Individual Patient Expanded Access IND of Hope Biosciences Autologous Adipose-derived Mesenchymal Stem Cells for Treatment of SCI

NCT ID: NCT03925649

Last Updated: 2025-09-29

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

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Recruitment Status

NO_LONGER_AVAILABLE

Study Classification

EXPANDED_ACCESS

Brief Summary

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This study is expanded access to an Investigational New Drug (IND) for an individual patient with spinal cord injury (SCI) at cervical spine 5-6 (C 5-6) designed to provide access to autologous adipose-derived mesenchymal stem cells (HB-adMSCs)

Detailed Description

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This is an expanded access single-dose study with the primary goal of treatment submitted at the request of an individual patient with complete C5-6 spinal cord injury (SCI) resulting in quadriplegia who does not qualify for any current clinical trials and for whom there are no other FDA approved fully restorative treatments. The overall objective of this study is to evaluate patient's response, adverse events and serious adverse events (AE/SAEs), and cell expansion characteristics of a single intravenous (IV) infusion of autologous adipose-derived mesenchymal stem cells (HB-adMSCs) in a subject with complete SCI resulting in quadriplegia.

Conditions

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Spinal Cord Injury at C5-C7 Level

Interventions

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HB-adMSCs

single infusion of HB-adMSCs

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Cognitively intact, capable of giving informed consent
* Clinical diagnosis of a non-penetrating traumatic SCI
* Asia Impairment Scale grade of A, B, or C

Exclusion Criteria

1. Prior history of:

* Brain injury
* Recent or ongoing infection
* Clinically significant cardiovascular, lung, renal, hepatic or endocrine disease,
* Neurodegenerative disorders
* Cancer
* Immunosuppression as defined by WBC\<3,000 cells/ml at baseline screening,
* HIV+
* Chemical or ETOH dependency
2. Having a contraindication to MRI scans
3. Other acute or chronic medical conditions that, in the opinion of the investigator, may increase the risks associated with study participation or HB-adMSC administration
4. Participation in other interventional research studies
5. Unwillingness to return for follow-up visits
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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The University of Texas Health Science Center, Houston

OTHER

Sponsor Role collaborator

Hope Biosciences LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Memorial Hermann Hospital-Clinical Research Unit (MMH-CRU)

Houston, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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HBSCI01

Identifier Type: -

Identifier Source: org_study_id

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