- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07705464
Safety Study of Intravenous MiraMSC in Older Adults With Mild to Moderate Frailty Syndrome
A Phase I, Open-Label Study to Evaluate the Safety and Tolerability of MiraMSC Administered Intravenously in Elderly Subjects With Mild to Moderate Frailty Syndrome
Przegląd badań
Szczegółowy opis
Frailty syndrome (FS) is an age-related clinical condition characterized by reduced physiological reserve and increased vulnerability to adverse health outcomes, including falls, hospitalization, disability, and mortality. Despite its growing prevalence in the aging population, effective treatment options for frailty syndrome remain limited.
MiraMSC-FS-001 is an investigational product consisting of allogeneic umbilical cord-derived mesenchymal stem cells (UCMSCs). Preclinical studies have demonstrated the immunomodulatory, anti-inflammatory, and regenerative properties of UCMSCs, supporting their clinical evaluation as a potential treatment for frailty syndrome. In addition, GLP toxicology studies demonstrated a favorable nonclinical safety profile for MiraMSC-FS-001, supporting its further clinical evaluation in humans.
This Phase I, open-label, dose-escalation study will evaluate the safety and tolerability of intravenous MiraMSC-FS-001 in older adults with mild to moderate frailty syndrome. Eligible participants will receive intravenous MiraMSC-FS-001 according to the study protocol and will undergo scheduled safety evaluations throughout the study. The results of this study are expected to provide clinical safety information to support the further development of MiraMSC-FS-001.
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 1
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Chin-Chung Lin
- Numer telefonu: +886-3-358999
- E-mail: oscar.lin@miracle-bio.com
Kopia zapasowa kontaktu do badania
- Nazwa: Che-Chia Liu
- Numer telefonu: +886-3-358999
- E-mail: aaron.liu@miracle-bio.com
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
Subjects will be eligible for enrollment in the study only if they meet ALL the following criteria at time of Screening:
- Subjects aged ≥ 60 through ≤ 85 years old.
- Subjects with clinical diagnosis of mild to moderate Frailty Syndrome as assessed by the Investigator with a Clinical Frailty Scale score between 4 to
6. 3. Subject will not start any new treatment for this condition during the study.
- The new treatment refers to any clinical study of new investigational therapies or any other stem cell therapies. Subject will be allowed to continue ongoing medications and therapies that are not prohibited treatment as listed in Section 6.4.1 and are deemed necessary by the Investigator for appropriate medical care. Minor modifications or dose adjustments to ongoing frailty- related treatments that were initiated prior to study enrollment and are not prohibited by the protocol may be implemented if deemed necessary by the Investigator for appropriate care; such adjustments will not be considered the initiation of a new treatment. ** 4. Subjects with body weight between 40 to 90 kg. 5. Subject is willing to provide written informed consent to participate in the study after reading the informed consent form and the information provided.
Exclusion Criteria:
Subjects meeting ANY of the following criteria at time of Screening will be excluded from enrollment:
- Subjects unwill ing or unable to perform any of the assessments required by endpoint analysis.
- Subjects who have a diagnosis of any disabling neurologic disorder including, but not limited to: Parkinson's disease, Amyotrophic Lateral Sclerosis, multiple sclerosis, stroke or dementia.
- Subjects who have a score on the Mini-Mental State Examination (MMSE) of 24 or below.
Subjects who have a significant comorbid medical condition(s) including, but not limited to:
- Severe kidney disease requiring hemodialysis or peritoneal dialysis;
- Advanced liver disease such as severe liver cirrhosis;
- Severe congestive heart failure (NYHA class 3 and 4);
- Severe pulmonary dysfunction, including severe chronic obstructive pulmonary disease stage III or IV (Gold classification)
- Subjects who have a clinical history of malignancy within 5 years (i.e., patients with prior malignancy must be disease free for 5 years), except curatively-treated basal cell carcinoma or in situ carcinomas.
- Subjects using chronic immunosuppressant therapy, including corticosteroids (> 5 mg/day of prednisone, or equivalent), or TNF-alpha antagonists.
- Subjects on chronic immunosuppressive transplant therapy.
- Subjects who have participated in another clinical study of new investigational therapies within 6 months prior to screening.
- Subjects who have received any other stem cell therapy within 12 months prior to screening.
- Subjects with known allergy or hypersensitivity to any component of the formulation and cellular therapies (i.e., penicillin or streptomycin).
- Subjects who have a history of drug or alcohol abuse within the past 3 years.
- Subjects who are known to be infected with HIV.
- Subjects currently in hospital stay.
Subjects who have a significant illness as judged by principal investigator (PI) including, but not limited to:
- Psychiatric illness
- Uncontrolled hypertension or hypotension
- Unstable cardiac arrhythmia
- Active Hepatitis B, Hepatitis C infections
- Subjects who have any condition that in the opinion of the Principal investigator limits lifespan to < 1 year.
- Subjects who have any other condition that, in the opinion of the investigator, may compromise the safety or compliance of the patient or preclude successful completion of the study.
- Subjects with known or suspected bleeding disorders (including but not limited to hemophilia, von Willebrand disease, or platelet function disorders), or clinically significant coagulopathy (including abnormal PT, PTT, or INR) at screening.
- Subjects receiving medications that may increase the risk of bleeding or coagulopathy (such as anticoagulants, antiplatelet agents, or thrombolytics), unless medically necessary and approved by the Medical Monitor on a case- by-case basis.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie sekwencyjne
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: MiraMSC-FS-001
Participants will receive intravenous MiraMSC-FS-001
|
MiraMSC-FS-001 is an investigational biological product consisting of allogeneic umbilical cord-derived mesenchymal stem cells (UCMSCs). Two treatment cohorts are included: Cohort 1: 9 × 10⁷ cells per dose, administered by intravenous infusion every 2 weeks for a total of 3 doses (total dose: 2.7 × 10⁸ cells). Cohort 2: 9 × 10⁷ cells per dose, administered by intravenous infusion every 2 weeks for a total of 6 doses (total dose: 5.4 × 10⁸ cells). |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Maximum Feasible Dose (MFD) of MiraMSC-FS-001
Ramy czasowe: Within 14 days after the last study treatment administration (3-dose cohort: last dose on Day 28; 6-dose cohort: last dose on Day 70).
|
Maximum Feasible Dose (MFD) determined based on the occurrence of dose-limiting toxicities (DLTs) after intravenous administration of MiraMSC-FS-001.
|
Within 14 days after the last study treatment administration (3-dose cohort: last dose on Day 28; 6-dose cohort: last dose on Day 70).
|
|
Incidence of dose-limiting toxicities (DLTs) and treatment-emergent adverse events (TEAEs)
Ramy czasowe: Baseline through Week 52
|
Safety and overall tolerability of MiraMSC-FS-001 will be evaluated based on the incidence and nature of dose-limiting toxicities (DLTs), the incidence of treatment-emergent adverse events (TEAEs), the incidence of withdrawals due to adverse events (AEs), changes/shifts in laboratory values, changes in vital signs, and changes in physical examination findings.
|
Baseline through Week 52
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Exercise performance measured by 6-minute walk test (6MWT) total distance
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The Six-Minute Walk Test (6MWT) measures the total distance walked in six minutes on a hard, flat surface.
Greater walking distance indicates better exercise performance.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Hand grip strength measured by maximum force using a hand dynamometer
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Hand grip strength is measured as the maximum force using a hand dynamometer.
Higher values indicate greater muscle strength.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Physical performance measured by Short Physical Performance Battery (SPPB) total score
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The Short Physical Performance Battery (SPPB) assesses lower extremity physical function.
Total scores range from 0 to 12, with higher scores indicating better physical performance.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Clinical Frailty Scale (CFS) score
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The Clinical Frailty Scale (CFS) assesses the overall level of frailty.
Scores range from 1 to 9, with higher scores indicating greater frailty.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Quality of life measured by Falls Efficacy Scale-International (FES-I) questionnaire score
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The Falls Efficacy Scale-International (FES-I) assesses concern about falling during daily activities.
Scores range from 16 to 64, with higher scores indicating greater concern about falling.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Physical function measured by PROMIS Physical Function Short Form 20a score
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function Short Form 20a assesses self-reported physical function.
Total raw scores are converted to standardized T-scores (mean = 50, standard deviation = 10), with higher T-scores indicating better physical function.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Quality of life measured by 36-Item Short Form (SF-36) survey score
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
The 36-Item Short Form Survey (SF-36) assesses health-related quality of life.
Scores range from 0 to 100, with higher scores indicating better health-related quality of life.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Mean change from baseline in superoxide dismutase (SOD) level
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Serum superoxide dismutase (SOD) level.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Mean change from baseline in tumor necrosis factor-alpha (TNF-α) level
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Serum tumor necrosis factor-alpha (TNF-α) level.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Mean change from baseline in creatine phosphokinase (CPK) level
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Serum creatine phosphokinase (CPK) level.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
|
Mean change from baseline in N-terminal pro-B-type natriuretic peptide (NT-proBNP) level
Ramy czasowe: Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) level.
|
Baseline, End of Treatment, Follow-up 1 (Week 24), Follow-up 2 (Week 36), and Follow-up 3 (Week 52)
|
Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- MiraMSC-FS-001
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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