Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06600581
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-02
Brief Title:
Safety and Efficacy of IMM01-STEM Against Placebo on Muscle Performance in Seniors With Obesity and Muscle Weakness
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Randomized Adaptive Study for Safety and Efficacy of Pluripotent Cell Secretome on Muscle Performance in Seniors With Sarcopenic Obesity
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Placebo controlled study for safety and efficacy of IMM01-STEM on muscle performance in seniors with obesity and muscle weakness
Detailed Description:
This will be a two-phase placebo-controlled dose expansion study that begins with 4 parallel dosing groups and one placebo control group phase IIa The treatment period and follow up will last 16 weeks then an interim adaptation will initiate the second phase of the study IIb The study will target safety parameters body composition and muscle strength and function Additional metabolic inflammatory and muscle-adipose crosstalk markers will be monitored
During screening a wearable activity tracker will be assigned to each participant to establish a baseline of daily physical activity
The treatment will be administered by intramuscular IM in a regimen of two injections per week with 2-3 days intervals between injections for 4 weeks The dosing groups vary by IMM01-STEM total protein and will be adjusted for identical volumes or equivalent saline volume for placebo The proposed doses will be 05 mg administered twice per week 1 mg once per week alternating with a placebo given on the second visit of the week 1 mg twice per week and 2 mg once per week also alternating with placebo
Each participant will be evaluated at baseline at the time of treatment administration during the treatment period then monthly until the end of trial
Interim analysis with the purpose of design adaptation will be performed after 10 participants from each group have completed treatment This point will be marked by the date when the final participant to enroll has completed the final treatment on Week 12 This would occur about 16 weeks after the final participant starts treatment
Statistical analysis will be performed on all recorded outcomes All participants will continue to be followed-up per protocol for additional 8 weeks
Post-adaptation enrollment will be restarted in accordance with the new randomization rules in a 2-arm placebo-controlled study IIb The best responding dose will be chosen or the most convenient treatment lowest dose less frequent administration in the case that all treatment arms responded equally at interim analysis An amended clinical protocol will be submitted prior initiation of the phase IIb study
Study participants will sign a written Informed Consent Form ICF prior to any study-related procedures Treatment must begin within 28 days of signing the ICF during which participant screening and any necessary drug wash-out period must be completed Screening assessments will be conducted as specified in the Schedule of Activities of the protocol after which the study participants eligibility will be determined based on the inclusion and exclusion criteria
Site staff will administer study medication by IM injection in the gluteal area using a small-gauge needle at all scheduled treatment visits If gluteal area is not feasible alternatively im injection can be administered in the quadriceps or deltoid area After each administration of study medication participants will be observed for 1 hour to monitor for acute injection-related reactions and other early onset treatment-related AEs
During screening a wearable activity tracker will be assigned to each participant to establish a baseline of daily physical activity
The treatment will be administered by intramuscular IM in a regimen of two injections per week with 2-3 days intervals between injections for 4 weeks The dosing groups vary by IMM01-STEM total protein and will be adjusted for identical volumes or equivalent saline volume for placebo The proposed doses will be 05 mg administered twice per week 1 mg once per week alternating with a placebo given on the second visit of the week 1 mg twice per week and 2 mg once per week also alternating with placebo
Each participant will be evaluated at baseline at the time of treatment administration during the treatment period then monthly until the end of trial
Interim analysis with the purpose of design adaptation will be performed after 10 participants from each group have completed treatment This point will be marked by the date when the final participant to enroll has completed the final treatment on Week 12 This would occur about 16 weeks after the final participant starts treatment
Statistical analysis will be performed on all recorded outcomes All participants will continue to be followed-up per protocol for additional 8 weeks
Post-adaptation enrollment will be restarted in accordance with the new randomization rules in a 2-arm placebo-controlled study IIb The best responding dose will be chosen or the most convenient treatment lowest dose less frequent administration in the case that all treatment arms responded equally at interim analysis An amended clinical protocol will be submitted prior initiation of the phase IIb study
Study participants will sign a written Informed Consent Form ICF prior to any study-related procedures Treatment must begin within 28 days of signing the ICF during which participant screening and any necessary drug wash-out period must be completed Screening assessments will be conducted as specified in the Schedule of Activities of the protocol after which the study participants eligibility will be determined based on the inclusion and exclusion criteria
Site staff will administer study medication by IM injection in the gluteal area using a small-gauge needle at all scheduled treatment visits If gluteal area is not feasible alternatively im injection can be administered in the quadriceps or deltoid area After each administration of study medication participants will be observed for 1 hour to monitor for acute injection-related reactions and other early onset treatment-related AEs
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None