Phase IIb Trial to Evaluate Longeveron Mesenchymal Stem Cells to Treat Aging Frailty

Phase 2

Completed

• Conditions: Aging Frailty
• Interventions: Biological: Longeveron Mesenchymal Stem Cells (LMSCs); Other: Placebo

• Registration Number: NCT03169231
• Lead Sponsor: Longeveron Inc.

Brief Summary

This is a randomized, placebo-controlled, double-blind, parallel arm, multi-center Phase 2b study.

Detailed Description

The objectives of this study are to assess safety and efficacy of Longeveron Mesenchymal Stem Cells (LMSCs) compared to placebo on 1) functional mobility and exercise tolerance, 2) patient-reported physical function, and 3) the inflammatory cytokine biomarker tumor necrosis factor (TNF-alpha).

Study Timeline

• Study First Submitted: 2017-05-24
• Study First Submitted QC: 2017-05-25
• Study First Posted: 2017-05-30
• Study Start: 2017-07-06
• Primary Completion: 2021-09-30
• Study Completion: 2021-09-30
• Status Verified: 2022-03
• Last Update Submitted: 2022-03-04
• Last Update Posted: 2022-03-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

1. Be willing and able to provide written informed consent and comply with all procedures required by the Protocol.
2. Be >70 and < 85 years of age at the time of signing the Informed Consent Form.
3. Have a Canadian Study on Health and Aging (CSHA) Clinical Frailty Scale score of 5 "mildly frail" or 6 "moderately frail".
4. Have a 6 minute walk distance of > 200m and < 400 m. Distances of two 6MWTs are to be within 15% of each other.
5. Have a serum TNF-alpha level > 2.5 pg/mL

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Exclusion Criteria

1. Be unwilling or unable to perform any of the assessments required by the protocol.

2. Have a diagnosis of any disabling neurologic disorder, including, but not limited to, Parkinson's disease, Amyotrophic Lateral Sclerosis, multiple sclerosis, cerebrovascular accident with residual deficits (e.g., muscle weakness or gait disorder), or diagnosis of dementia.

3. Have a score of 24 or lower on the Mini Mental State Examination (MMSE)

4. Have poorly controlled blood glucose levels (HbA1c >8.0%).

5. Have a clinical history of malignancy within 2.5 years (i.e., subjects with prior malignancy must be cancer free for 2.5 years) except curatively-treated basal cell carcinoma, melanoma in situ or cervical carcinoma.

6. Have any condition that in the opinion of the Principal Investigator limits lifespan to < 1 year.

7. Have autoimmune disease (e.g. rheumatoid arthritis, systemic lupus erythematosus).

8. Be using chronic immunosuppressant therapy such as high-dose corticosteroids or TNF-alpha antagonists (prednisone use at doses of < 5 mg daily is allowed).

9. Test positive for hepatitis B virus

   a. If the subject tests positive for anti-hepatitis B core antigen (HBc) or anti-HBs, they must be currently receiving treatment for Hepatitis B prior to infusion and remain on treatment throughout the study.

10. Test positive for verimic Hepatitis C virus, HIV1/2, or syphilis

11. Have a resting blood oxygen saturation of <93% (measured by pulse oximetry).

12. Known or suspected alcohol or drug abuse within three years preceding Screening

13. Have a known hypersensitivity to dimethyl sulfoxide (DMSO).

14. Be an organ transplant recipient (other than transplantation for corneal, bone, skin, ligament, or tendon).

15. Be actively listed (or expected future listing) for transplant of any organ (other than corneal transplant).

16. Have any clinically important abnormal screening laboratory values, including, but not limited to:

    1. Hemoglobin <10.0 g/dL,
    2. White blood cell <2,500/ul, or platelet count <100,000/ul
    3. Liver dysfunction evidenced by enzymes (AST and ALT) > 3 times the upper limit of normal (ULN)
    4. Coagulopathy (INR>1.3) not due to a reversible cause (e.g. warfarin and/or Factor Xa inhibitors).

17. Uncontrolled hypertension (resting systolic blood pressure >180 mm Hg or diastolic blood pressure of > 110 mm Hg at Screening)

18. Have unstable angina pectoris, uncontrolled or severe peripheral artery disease within the previous 3 months.

19. Have congestive heart failure defined by NYHS (New York Heart Association) Class III or IV, or an ejection fraction of <25%.

20. Have a coronary artery bypass surgery, angioplasty, or peripheral vascular disease revasculation or a myocardial infarction within previous 3 months.

21. Have severe pulmonary dysfunction: acute exacerbation of chronic obstructive lung disease stage III or IV (Gold classification), and/or PaO2 levels <60 mmHg.

22. Have a partial ileal gastric bypass, or other significant intestinal malabsorption.

23. Have advanced liver or renal disease

24. Have cognitive or language barriers that prohibit obtaining informed consent or any study elements.

25. Be currently hospitalized, or living in an assisted living facility or a long-term care facility.

26. Be currently participating (or participated within the previous 30 days of consent) in an investigational therapeutic or device trial.

27. 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 patient's participation for the full duration of the study.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Study Group B	Longeveron Mesenchymal Stem Cells (LMSCs)	Single peripheral IV infusion of 50 million Longeveron Mesenchymal Stem Cells (LMSCs)
Study Group C	Longeveron Mesenchymal Stem Cells (LMSCs)	Single peripheral IV infusion of 100 million Longeveron Mesenchymal Stem Cells (LMSCs)
Study Group D	Longeveron Mesenchymal Stem Cells (LMSCs)	Single peripheral IV infusion of 200 million Longeveron Mesenchymal Stem Cells (LMSCs)
Study Group E	Placebo	Single peripheral IV infusion of placebo.
Study Group A	Longeveron Mesenchymal Stem Cells (LMSCs)	Single peripheral IV infusion of 25 million Longeveron Mesenchymal Stem Cells (LMSCs)

Primary Outcome Measures

Name	Time	Method
Change from baseline in 6 Minute Walk Test (6MWT) compared to placebo	Baseline and 180 days post-infusion	Change from baseline in 6MWT compared to placebo at 180 days post-infusion

Secondary Outcome Measures

Name	Time	Method
Change in patient reported outcome of overall physical function capacity using the PROMIS-Physical Function-Short Form 20a compared to placebo	180 days post-infusion	Change from baseline in physical function will be measured to assess Patient-Reported Outcome Measurement compared to placebo at 180 days post infusion.
Change in TNF-alpha compared to placebo	180 days post-infusion	Change in serum TNF-alpha compared to placebo

Trial Locations

Locations (7)

Soffer Health Institute; 🇺🇸 Aventura, Florida, United States

Panax Clinical Research; 🇺🇸 Miami Lakes, Florida, United States

Clinical Physiology Associates; 🇺🇸 Fort Myers, Florida, United States

Vista Health Research; 🇺🇸 Miami, Florida, United States

Clinical Research of South Florida; 🇺🇸 Coral Gables, Florida, United States

Miami VA Healthcare System; 🇺🇸 Miami, Florida, United States

Advanced Research for Health Improvement, LLC; 🇺🇸 Naples, Florida, United States