Pancreatic CancerNCT04087889
Individual Patient Expanded Access IND of Hope Biosciences First Blood Relative Allogeneic Adipose-derived Mesenchymal Stem Cells (HB-adMSCs) for Pancreatic Cancer
A study testing HB-adMSCs in people with Pancreatic Cancer, run by Hope Biosciences LLC at 1 site in United States.
Trial summary
The drug for this submission is Hope Biosciences' allogeneic, first blood relative, adipose-derived culture-expanded mesenchymal stem cells (HB-adMSCs) for the treatment of a single patient with Pancreatic Cancer (PC). Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Pancreatic Cancer
- What is being tested?
- HB-adMSCs
- 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 Any age
- Men only
- Child, Adult, Older adult
Who may be able to join
- Documented diagnosis of Pancreatic Cancer
- Hemodynamically stable
Who cannot join
- 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.
- Any abnormal, inexplicable laboratory result with no obvious cause defined.
- Participation in other interventional research studies. Unwillingness to return for follow-up visits
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Individual Patient Expanded Access IND of Hope Biosciences Allogeneic First Blood Relative Adipose-derived Mesenchymal Stem Cells (HB-adMSCs) for Pancreatic Cancer
The drug for this submission is Hope Biosciences' allogeneic, first blood relative, adipose-derived culture-expanded mesenchymal stem cells (HB-adMSCs) for the treatment of a single patient with Pancreatic Cancer (PC). PC is an extremely infiltrative neoplasm that usually presents with vascular and perineural invasion in surgically resected tumors. Metastases to lymph nodes, liver and distant sites are all very common. Its incidence has markedly increased over the past several decades and ranks as the fourth leading cause of cancer death in the United States. Despite the high mortality rate associated with pancreatic cancer, its etiology is poorly understood. PC patients experience physiological symptoms such as anemia, ascites, severe fatigue, pain, cachexia, weakness, insomnia, confusion, and memory loss. The aggressive nature of PC leads to rapid deterioration of patients' quality of life and diminished ability to participate in treatment.
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 infusion. Subsequent treatments will occur weekly for the first 8 infusions, followed by 4 infusion that occur 2 weeks apart. The total number of infusions will be 12.
On each of these visits, the subject will receive one allogeneic HB-adMSC infusion of 200 million (2 x 10^8 cells) total cells suspended in 250 mL normal saline for IV infusion. Every infusion visit will include the following procedures:
- Review of medical history,
- Complete Physical exam (Week 1, 4, 10, 20, and 52),
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Weight measurement
- A verification of patient consent will be verbally performed
- *When applicable (Week 4, 7, 10, 14, 20 and 52): A urine and blood sample for clinical labs including:
- CBC with diff.,
- CMP,
- Coagulation Panel,
- TNF-a
- IL-6
- CA 19-9
- LDH
- The HB-adMSC infusion will be given via IV.
- The subject will then be monitored for a minimum of 2hr after infusion.
- 24-hour telephone assessment for adverse events
- Video Documentation
Vital signs will be continuously monitored during the infusion and recorded at 15 minutes intervals during the first hour. Vital signs will be recorded at the end of the infusion and every 30 minutes x 2 hours or more frequently if clinically indicated. The subject will be contacted by telephone 24hr. after the infusion visit to determine if any adverse events have occurred.
*Please note that blood and urine sample during the intervention period will only be required for the visits corresponding to weeks 4, 7, 10, 14, 20 and 52. During these visits, these samples will always be taken before the infusion is started. Refer to Table 1. Schedule of assessments for more details.
Follow-up Visits week 4,7, 10, 14, 20, and 52
The subject will undergo the following procedures at each follow-up visit without infusion:
- Review and update medical history,
- Update concomitant medications list
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Complete physical exam (Week 1, 4, 10, 20, and 52)
- A urine and blood sample for clinical labs including:
- CBC with diff.,
- CMP,
- Coagulation Panel,
- TNF-a
- IL-6
- CA 19-9
- LDH
- Adverse event monitoring.
In addition, visits 13 and 14 (week 20 and 52) will include CT Scans of the chest, abdomen and pelvis. This procedure could be done up to 7 days before or after the actual visit day, depending on availability and schedule of the imaging center. If a CT Scan has been done as standard of care within 30 days of these visits, it would meet the requirement for this assessment.
- Conditions
- Pancreatic Cancer
- Being tested
- HB-adMSCs
- Keywords
- Cancer, Pancreas, Adenocarcinoma
- Medical subject headings
- Pancreatic Neoplasms, Neoplasms, Adenocarcinoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HB-adMSCsBiological
Culture-expanded, adipose-derived mesenchymal stem cells donated by first blood relative
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Sep 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pancreatic CancerStudies 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 LLC
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04087889
- Sponsor's protocol ID
- HBPC01
- Status last verified
- Sep 2025
- First submitted
- 10 Sep 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 Hope Biosciences Allogeneic First Blood Relative Adipose-derived Mesenchymal Stem Cells (HB-adMSCs) for Pancreatic Cancer
- ClinicalTrials.gov ID
- NCT04087889
- Acronym / sponsor ID
- HBPC01
- Conditions
- Pancreatic Cancer
- Keywords
- Cancer, Pancreas, Adenocarcinoma
- Study type
- Expanded access
- Recruitment status
- No Longer Available
- Lead sponsor
- Hope Biosciences LLCIndustry (pharma, biotech, devices)
- First posted
- 12 Sep 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.
The drug for this submission is Hope Biosciences' allogeneic, first blood relative, adipose-derived culture-expanded mesenchymal stem cells (HB-adMSCs) for the treatment of a single patient with Pancreatic Cancer (PC). PC is an extremely infiltrative neoplasm that usually presents with vascular and perineural invasion in surgically resected tumors. Metastases to lymph nodes, liver and distant sites are all very common. Its incidence has markedly increased over the past several decades and ranks as the fourth leading cause of cancer death in the United States. Despite the high mortality rate associated with pancreatic cancer, its etiology is poorly understood. PC patients experience physiological symptoms such as anemia, ascites, severe fatigue, pain, cachexia, weakness, insomnia, confusion, and memory loss. The aggressive nature of PC leads to rapid deterioration of patients' quality of life and diminished ability to participate in treatment.
Detailed description
Once the eligibility is confirmed, approximately 1-3 weeks after the screening/baseline visit, the subject will return for the first infusion. Subsequent treatments will occur weekly for the first 8 infusions, followed by 4 infusion that occur 2 weeks apart. The total number of infusions will be 12.
On each of these visits, the subject will receive one allogeneic HB-adMSC infusion of 200 million (2 x 10^8 cells) total cells suspended in 250 mL normal saline for IV infusion. Every infusion visit will include the following procedures:
- Review of medical history,
- Complete Physical exam (Week 1, 4, 10, 20, and 52),
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Weight measurement
- A verification of patient consent will be verbally performed
- *When applicable (Week 4, 7, 10, 14, 20 and 52): A urine and blood sample for clinical labs including:
- CBC with diff.,
- CMP,
- Coagulation Panel,
- TNF-a
- IL-6
- CA 19-9
- LDH
- The HB-adMSC infusion will be given via IV.
- The subject will then be monitored for a minimum of 2hr after infusion.
- 24-hour telephone assessment for adverse events
- Video Documentation
Vital signs will be continuously monitored during the infusion and recorded at 15 minutes intervals during the first hour. Vital signs will be recorded at the end of the infusion and every 30 minutes x 2 hours or more frequently if clinically indicated. The subject will be contacted by telephone 24hr. after the infusion visit to determine if any adverse events have occurred.
*Please note that blood and urine sample during the intervention period will only be required for the visits corresponding to weeks 4, 7, 10, 14, 20 and 52. During these visits, these samples will always be taken before the infusion is started. Refer to Table 1. Schedule of assessments for more details.
Follow-up Visits week 4,7, 10, 14, 20, and 52
The subject will undergo the following procedures at each follow-up visit without infusion:
- Review and update medical history,
- Update concomitant medications list
- Weight
- Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
- Complete physical exam (Week 1, 4, 10, 20, and 52)
- A urine and blood sample for clinical labs including:
- CBC with diff.,
- CMP,
- Coagulation Panel,
- TNF-a
- IL-6
- CA 19-9
- LDH
- Adverse event monitoring.
In addition, visits 13 and 14 (week 20 and 52) will include CT Scans of the chest, abdomen and pelvis. This procedure could be done up to 7 days before or after the actual visit day, depending on availability and schedule of the imaging center. If a CT Scan has been done as standard of care within 30 days of these visits, it would meet the requirement for this assessment.
Study design
Who may qualify
- Sex
- Male only
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- Documented diagnosis of Pancreatic Cancer
- Hemodynamically stable
Key exclusion criteria (4 listed)
- 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.
- Any abnormal, inexplicable laboratory result with no obvious cause defined.
- Participation in other interventional research studies. Unwillingness to return for follow-up visits
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-adMSCsCulture-expanded, adipose-derived mesenchymal stem cells donated by first blood relative | 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.
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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 Pancreatic Cancer, run by Hope Biosciences LLC 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 4 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.