AzTrials
AzTrials

Cardiovascular DiseasesPhase 1/2NCT06087848

A Study to Evaluate Mesenchymal Stem Cell Product StromaForte's Effect on Cardiovascular Events

A Phase 1/2 study testing Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte) in people with Cardiovascular Diseases, run by Cellcolabs Clinical LTD. at 1 site in The Bahamas.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

The goal of this phase I/II clinical trial is to evaluate the safety and preventive effect of intravenous infusion of human allogeneic bone-marrow-derived mesenchymal stromal cell product StromaForte in study participants. Read more about this study

Who is it for?
Ages 25 to 85 yearsHealthy volunteers can take part
Conditions the study is for
Cardiovascular Diseases
What is being tested?
Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte)
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteThe Bahamas
Study dates
7 Oct 2023to 6 Oct 2029
Phase
Phase 1/2
Are there results?
Not yet: the study is under way

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 25 to 85 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Willing and able to provide written informed consent and comply with all procedures required by the protocol.
  • Aged ≥ 25 to 85 years at the time of signing the informed consent form.
  • Subjects with pre-morbid or stable morbid medical conditions, not requiring significant changes to their current medical therapy for > 6 months prior to enrolling in this study, are eligible

Who cannot join

  • Unwilling or unable to perform any of the assessments required by the protocol.
  • Have end stage liver or renal disease.
  • Have a clinical history of malignancy within 2.5 years (i.e., study participants with prior malignancy must be cancer free for 2.5 years) except curatively treated basal cell carcinoma, melanoma in situ, or cervical carcinoma.
  • Have any condition that limits lifespan to < 1 year according to the Principal Investigator's discretion.
  • Hepatitis B virus positive
  • Viraemic Hepatitis C virus, HIV-1/2 or syphilis positive
Show all 15Show fewer
  • Have unstable angina pectoris, uncontrolled or severe peripheral artery disease within the previous 2 months.
  • Have congestive heart failure defined by New York Heart Association (NYHA) Class IV, or an ejection fraction of <25%.
  • Uncontrolled hypertension (resting systolic blood pressure >220 mm Hg or diastolic blood pressure of > 150 mm Hg at screening)
  • Have coronary artery bypass surgery, angioplasty, peripheral vascular disease revascularization, or a myocardial infarction within the previous month.
  • Have acute exacerbation of chronic obstructive lung disease stage III or IV (Gold classification), Have cognitive or language barriers that prohibit obtaining informed consent or any study elements.
  • Severe acute infection at time of screening and treatment with study drug
  • Pregnant or Breastfeeding
  • Currently participating (or participated within the previous 30 days of consent) in an investigational therapeutic or device trial.
  • Have a history or current evidence of any condition, therapy, laboratory abnormality, or other circumstance that might confound the results of the study or interfere with the study participant's participation for the full duration of the study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

The Bahamas1 site, 1 recruiting
  • Live Well

    Nassau, The Bahamas

    Darius Bain, MD, info@livewellbahamas.com

    Recruiting

About this study

Official title: A Longitudinal Open-Label Multi-center Single-Arm Phase I/IIa Study to Evaluate the Safety and Preventive Effect on Cardiovascular Events of Human Allogenic Bone-Marrow-Derived Mesenchymal Stromal Cell Product, StromaForte, in Study Participants.

The goal of this phase I/II clinical trial is to evaluate the safety and preventive effect of intravenous infusion of human allogeneic bone-marrow-derived mesenchymal stromal cell product StromaForte in study participants. The main questions it aims to answer are:

To assess the safety and tolerability after 28 days of injection by reporting the number of adverse events assessed by Common Terminology Criteria For Adverse Events (CTCAE) To evaluate the effects of Mesenchymal stem cells on Prevention of Cardiovascular Events by following the reported incidence of cardiovascular events amongst study participants up to five year post-injection Participants will receive 100 x 106 allogeneic bone marrow (BM)-derived Mesenchymal Stromal Cell (MSC) formulated in sodium chloride supplemented with human serum albumin to be given via slow intravenous infusion 100 million cells in approximately 30 min

Read the detailed description

Cardiovascular disease (CVD) is a group of disorders of the heart and blood vessels including, among other coronary heart, cerebrovascular, and peripheral arterial diseases that are difficult to reverse once clinically verified. According to the WHO, CVDs are the leading cause of death globally, taking an estimated 17.9 million lives each year. More than four out of five CVD deaths are due to heart attacks and strokes, and one third of these deaths occur prematurely in people under 70 years of age (1). The onset of CVD may seem binary for the individual patient, one day one is healthy and the next one has suffered an event such as a myocardial infarction or a stroke. Thereby a vast majority of the treatments are interventions when a cardiovascular event happens, and consequently preventative efforts are mostly secondary prevention oriented, and therapies are often reduced to a monitoring of symptoms.

However, while some people are genetically predisposed to develop CVDs, everyone is at risk. CVDs is a group of aging- related chronic diseases, similarly to diabetes and arthritis, with an earlier onset than an eventual cardiovascular event. The vascular pathophysiology leading up to the first CVD event has often been gradually developing asymptomatically over years, driven by among other things tissue inflammation, endothelial dysfunction, and increased blood pressure, before the individual becomes aware of it. It is widely shown that ageing related diseases, like CVDs, are a huge challenge for societies around the globe, and that these groups consume up to 70-80 % of healthcare resources. Thus, healthy longevity is not only of interest for the individual but to society as well. If we are to reach the UN Sustainable Development Goal (SGD) #3 - Good Health and Wellbeing, prevention of diseases at an earlier stage is thought to play a key role.

The concept of preventive medicine is in its prime but there is a need for more research and scientific evidence around how to foster healthy longevity by retarding or preventing, among other things, the chronic inflammation that often drives the development of ageing related diseases. Acknowledging the gradual development of CVD, not only secondary prevention but also primary preventative treatment is an interesting strategy to examine further. Stem cells hold promise for mitigating the risk factors and reducing the incidence of these major health conditions. Due to their anti-inflammatory, regenerative, and immunomodulatory effects MSCs are an especially interesting candidate of preventive treatments, i.e., even for individuals without clinical symptoms, since ageing related diseases and vascular degeneration are partly driven by inflammation accelerated or slowed down by individual lifestyle, comorbidities, inherited genetics, age, and many other factors.

The Mesoblast DREAM-HF study published in 2023, indicated that there may be a potential secondary preventative effect of MSC on CVD. Mesenchymal Precursor Cell (MPC) therapy with local injection in the heart muscle did not meet its primary and secondary endpoints but resulted in significant reduced risk for time-to-first Major Adverse Cardiac Event (MACE) defined as cardiovascular death, Myocardial Infarction (MI) or stroke over a mean follow-up of 30 months with the most benefit seen in patients with evidence of systemic inflammation. The study also demonstrated a strengthened heart function, which was measured by the left ventricular ejection fraction (LVEF) for patients receiving the treatment compared to the control group.

To investigate the preventive, mitigating, and/or retarding effects of MSCs for the gradual disease development and/or degeneration across multiple cohorts of different risks this study is designed to follow a large and diverse study participant population over a long period of time (five years). All enrolled study participants will be risk stratified and categorized into different cohorts based on the well-established cardiovascular risk assessment tool Atherosclerotic Cardiovascular Disease (ASCVD) Risk calculator developed by American College of Cardiology and complementary questionnaires. All enrolled study participants will receive an initial dose of 100 x 106 MSCs that can be repeated at a minimum interval of 3 months. The endpoints collected from enrolled study participants will be compared to baseline as well as with the expected rates/outcomes from risk matched cohorts/patients in relevant open label registries (Real World Data - RWD) across the globe.

The study will assess changes in study participants' risk and life/lifestyle (based on the gold standards) from baseline throughout the study to account for external factors that might impact the disease's development. The study will also identify subgroups of study participants based on the number of doses received and the treatment frequency to assess the potential cumulative effects of the MSCs to provide new insights around host and dose response. To have a rich dataset and a more accurate comparison to cohorts in other registries, the ambition is to include data from follow-up visits and, by written consent from the study participants, study participants own general medical records, health scans and additional blood works. Ultimately, this study seeks to investigate the safety and efficacy of MSC therapy for preventing cardiovascular diseases by comparing individuals of the same risk-level that have received a MSC treatment against matched controls from RWD

Being tested
Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte)
Medical subject headings
Cardiovascular Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte)Biological

    100 x 106 allogeneic bone marrow (BM)-derived Mesenchymal Stromal Cell (MSC) formulated in sodium chloride supplemented with human serum albumin to be given via slow intravenous infusion in approximately 30 min

Study groups in NCT06087848
Study groupRoleWhat they receive
MSC Intervention GroupExperimentalParticipants will receive 100 x 106 allogeneic bone marrow (BM)-derived Mesenchymal Stromal Cells in one intravenous infusion. Additional systemic treatments can be repeated after a minimum of 3 months and data will be collected to investigate the potential preventive benefits it provides for the above indications. Additional doses are optional for all study participants enrolled in the study and will be managed in a separate consenting process. Study participants opting for an extra dose must at the time of the extra dose meet the same inclusion and exclusion criteria as participants being included for the first dose
Receives: Biological: Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To evaluate the number of adverse events or severe adverse event assessed by Common Terminology Criteria For Adverse Events (CTCAE) of intravenous infusion of human allogeneic BM-derived MSCs product StromaForte for all study participants.

    To assess the safety of injection by reporting the number of adverse events or severe adverse event assessed by Common Terminology Criteria For Adverse Events (CTCAE) which is the Incidence of any treatment-emergent serious adverse events (TE-SAEs), defined as the composite of death, non-fatal pulmonary embolism, stroke, hospitalization for worsening dyspnea and clinically significant laboratory test abnormalities determined per the Investigator's judgment.

    Measured: 28 day post-infusion

Secondary outcomes (1)
  1. To evaluate the effects of MSCs on Prevention of Cardiovascular Events

    The secondary endpoint of this study is to evaluate the reported incidence of cardiovascular events among the study participants. Cardiovascular events include but are not limited to myocardial infarction (heart attack), stroke, coronary artery disease, heart failure, and peripheral arterial disease. By monitoring and documenting the occurrence of these events, the study aims to assess the impact of the intervention (e.g., treatment with mesenchymal stem cells) on reducing the overall burden of cardiovascular events in the study population.

    Measured: From baseline to 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Oct 2023
  2. Study start7 Oct 2023
  3. Primary completion6 Oct 2029 (estimated)
  4. Study completion6 Oct 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06087848
Sponsor's protocol ID
2023-001-BHS
Status last verified
Apr 2024
First submitted
4 Oct 2023
Last updated
19 Apr 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Human Allogeneic Bone-Marrow-Derived Mesenchymal Stromal Cell Product (StromaForte) in people with Cardiovascular Diseases, run by Cellcolabs Clinical LTD. at 1 site in The Bahamas.

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 3 inclusion and 15 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: looking for participants now, as of the sponsor's last update on 19 Apr 2024. 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 The Bahamas. 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.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To evaluate the number of adverse events or severe adverse event assessed by Common Terminology Criteria For Adverse Events (CTCAE) of intravenous infusion of human allogeneic BM-derived MSCs product StromaForte for all study participants. (time frame: 28 day post-infusion). It is what the study was designed to measure, not a finding.

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 19 Apr 2024.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in