Cerebral PalsyNCT04029896
Individual Patient Expanded Access IND of Hope Biosciences Autologous Adipose-derived Mesenchymal Stem Cells for the Treatment of Cerebral Palsy
A study testing HB-adMSCs in people with Cerebral Palsy, run by Hope Biosciences Research Foundation at 1 site in United States.
Trial summary
This is an Individual Patient Expanded Access Protocol of Autologous HB-adMSCs for the Treatment of Cerebral Palsy (CP) with the primary goal of treating 1 individual with CP who has exhausted all treatment options, his condition has not improved, his quality of life is severely affected by the condition and he has… Read more about this study
- Who is it for?
- Ages 3 years and older, men only
- Conditions the study is for
- Cerebral Palsy
- What is being tested?
- HB-adMSCs
- Type of treatment
- Injection or infusion
- How many people
- Not given
- Where
- 1 siteUnited States
- Study dates
- Start not givento not given
- Phase
- Expanded access
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 3 years and older
- Men only
- Child, Adult, Older adult
Who may be able to join
- Diagnosis of Cerebral Palsy
- 3 years and older.
Who cannot join
- Recent or ongoing infection
- Clinically significant cardiovascular, lung, renal, hepatic, or endocrine disease.
- Immunosuppression as defined by WBC < 3, 000 cells/ml at baseline screening.
- 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.
- Participation in other interventional research studies.
- Unwillingness to return for follow-up visits.
Trial locations and contacts
1 site in 1 country.
United States1 site
Hope Biosciences Stem Cell Research Foundation
Sugar Land, Texas, 77478
About this study
Official title: Individual Patient Expanded Access IND of Autologous Adipose-derived Mesenchymal Stem Cells for the Treatment of Cerebral Palsy
This is an Individual Patient Expanded Access Protocol of Autologous HB-adMSCs for the Treatment of Cerebral Palsy (CP) with the primary goal of treating 1 individual with CP who has exhausted all treatment options, his condition has not improved, his quality of life is severely affected by the condition and he has previously banked his mesenchymal stem cells. There are no FDA approved, fully restorative treatments for CP. The subject will receive 8 autologous HB-adMSC infusions of 50 million (50 x 10^6 cells) total cells. A protocol amendment to administer additional HB-adMSC infusions may be submitted for IRB/FDA for approval depending on the patient's response, AE/SAEs, and cell expansion characteristics.
Read the detailed description
Once the eligibility is confirmed, approximately 1-3 weeks after the screening/baseline visit, the subject will return for the first infusions. Subsequent treatments will occur every other week.
On each of these visits, the subject will receive one autologous HB-adMSC infusion of 50 million (50 x 10^6 cells) total cells. Every infusion visit will include the following procedures:
- Interval H\&P update,
- Weight
- Vital signs monitoring (Heart Rate, BP, Resp., Temp., SpO2),
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel, Serum Leptin),
- A verification of patient/LAR consent will be verbally performed,
- The HB-adMSC infusion will be given via IV over a 1 hour period.
- The subject will then be monitored for a minimum of 4hr.
- 24-hour telephone assessment for adverse events
- Video Documentation
Follow Up Visits Week 4, 8, 12 and 16 (Safety Assessments)
The patient will be assessed for adverse events 24 hours after each infusion with a follow up phone call. 4 weeks after the first infusion have occurred, the subject will return to the clinical site for an onsite safety assessment, which will be repeated at week 8, 12, and 16. Each one of these on-site safety assessments will include:
- Review and update medical history,
- Update concomitant medications list
- Video documentation
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Physical exam,
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin)
- SARAH assessment on Weeks 4, 12 and 16.
- Adverse event monitoring Follow Up Visit Week 26 (Safety Assessments)
- Review and update medical history, 2. Update concomitant medications list 3. Weight 4. Vital signs (Heart Rate, BP, Respirations, Temp., SpO2), 5. Physical exam, 6. A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin), 7. Brain MRI 8. The SARAH (motor-functional evaluation scale for children and adolescents with cerebral palsy) 9. Adverse event monitoring 10. Video documentation
Follow Up Visit Week 52 (Safety Assessments-End of Study)
- Review and update medical history,
- Update concomitant medications list
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Physical exam,
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin),
- Chest X ray (PA Single view)
- The SARAH (motor-functional evaluation scale for children and adolescents with cerebral palsy)
- Adverse event monitoring
- Video documentation
- Conditions
- Cerebral Palsy
- Being tested
- HB-adMSCs
- Keywords
- CP, stem cells, MSCs, spastic, paralysis, cerebral palsy
- Medical subject headings
- Cerebral Palsy, Muscle Spasticity, Paralysis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HB-adMSCsBiological
intravenous infusion of Hope Biosciences autologous adipose-derived stem cells
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jul 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cerebral PalsyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Expanded access
Sponsor and investigators
- Lead sponsor
- Hope Biosciences Research Foundation
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04029896
- Sponsor's protocol ID
- HBCP01
- Status last verified
- Sep 2025
- First submitted
- 19 Jul 2019
- Last updated
- 29 Sep 2025
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Individual Patient Expanded Access IND of Autologous Adipose-derived Mesenchymal Stem Cells for the Treatment of Cerebral Palsy
- ClinicalTrials.gov ID
- NCT04029896
- Acronym / sponsor ID
- HBCP01
- Conditions
- Cerebral Palsy
- Keywords
- CP, stem cells, MSCs, spastic, paralysis, cerebral palsy
- Study type
- Expanded access
- Recruitment status
- No Longer Available
- Lead sponsor
- Hope Biosciences Research FoundationIndustry (pharma, biotech, devices)
- First posted
- 23 Jul 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is an Individual Patient Expanded Access Protocol of Autologous HB-adMSCs for the Treatment of Cerebral Palsy (CP) with the primary goal of treating 1 individual with CP who has exhausted all treatment options, his condition has not improved, his quality of life is severely affected by the condition and he has previously banked his mesenchymal stem cells. There are no FDA approved, fully restorative treatments for CP. The subject will receive 8 autologous HB-adMSC infusions of 50 million (50 x 10^6 cells) total cells. A protocol amendment to administer additional HB-adMSC infusions may be submitted for IRB/FDA for approval depending on the patient's response, AE/SAEs, and cell expansion characteristics.
Detailed description
Once the eligibility is confirmed, approximately 1-3 weeks after the screening/baseline visit, the subject will return for the first infusions. Subsequent treatments will occur every other week.
On each of these visits, the subject will receive one autologous HB-adMSC infusion of 50 million (50 x 10^6 cells) total cells. Every infusion visit will include the following procedures:
- Interval H\&P update,
- Weight
- Vital signs monitoring (Heart Rate, BP, Resp., Temp., SpO2),
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel, Serum Leptin),
- A verification of patient/LAR consent will be verbally performed,
- The HB-adMSC infusion will be given via IV over a 1 hour period.
- The subject will then be monitored for a minimum of 4hr.
- 24-hour telephone assessment for adverse events
- Video Documentation
Follow Up Visits Week 4, 8, 12 and 16 (Safety Assessments)
The patient will be assessed for adverse events 24 hours after each infusion with a follow up phone call. 4 weeks after the first infusion have occurred, the subject will return to the clinical site for an onsite safety assessment, which will be repeated at week 8, 12, and 16. Each one of these on-site safety assessments will include:
- Review and update medical history,
- Update concomitant medications list
- Video documentation
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Physical exam,
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin)
- SARAH assessment on Weeks 4, 12 and 16.
- Adverse event monitoring Follow Up Visit Week 26 (Safety Assessments)
- Review and update medical history, 2. Update concomitant medications list 3. Weight 4. Vital signs (Heart Rate, BP, Respirations, Temp., SpO2), 5. Physical exam, 6. A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin), 7. Brain MRI 8. The SARAH (motor-functional evaluation scale for children and adolescents with cerebral palsy) 9. Adverse event monitoring 10. Video documentation
Follow Up Visit Week 52 (Safety Assessments-End of Study)
- Review and update medical history,
- Update concomitant medications list
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Physical exam,
- A urine and blood sample for clinical labs (CBC with diff., CMP, and Coagulation Panel and serum leptin),
- Chest X ray (PA Single view)
- The SARAH (motor-functional evaluation scale for children and adolescents with cerebral palsy)
- Adverse event monitoring
- Video documentation
Study design
Who may qualify
- Ages
- 3 years and older
- Sex
- Male only
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- Diagnosis of Cerebral Palsy
- 3 years and older.
Key exclusion criteria (6 listed)
- Recent or ongoing infection
- Clinically significant cardiovascular, lung, renal, hepatic, or endocrine disease.
- Immunosuppression as defined by WBC < 3, 000 cells/ml at baseline screening.
- 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.
- Participation in other interventional research studies.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HB-adMSCsintravenous infusion of Hope Biosciences autologous adipose-derived stem cells | Biological | – |
Primary outcome
Not reported in the source record.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Sep 2025.
- Hope BiosciencesLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing HB-adMSCs in people with Cerebral Palsy, run by Hope Biosciences Research Foundation at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 29 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2025.