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Anti-inflammatory agent

MYMD-1 600MG for Frailty

Phase 2
Waitlist Available
Led By Lon Lynn, DO
Research Sponsored by MyMD Pharmaceuticals, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 28 (8-24 hours post dose)

Summary

This trial tests MYMD1, a drug aimed at reducing inflammation, in older adults with muscle weakness and frailty. The drug works by lowering the chemicals that cause inflammation, potentially improving muscle strength.

Eligible Conditions
  • Frailty
  • Sarcopenia
  • Aging

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 28 (8-24 hours post dose)
This trial's timeline: 3 weeks for screening, Varies for treatment, and day 28 (8-24 hours post dose) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Demonstrate reduction of chronic inflammatory markers in participants treated with MYMD1
Capsule (pharmacologic)
Capsule (pharmacologic)
Secondary study objectives
Incidence of Treatment-Emergent Adverse Events

Trial Design

8Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Cohort 3: MYMD1 900mgExperimental Treatment1 Intervention
Subjects randomly assigned to the MYMD1 900mg cohort
Group II: Cohort 2: MYMD1 750mgExperimental Treatment1 Intervention
Subjects randomly assigned to the MYMD1 750 cohort
Group III: Cohort 1: MYMD1 600mgExperimental Treatment1 Intervention
Subjects randomly assigned to the MYMD1 600mg cohort
Group IV: Cohort 4: MYMD1 1050mgActive Control1 Intervention
Subjects randomly assigned to the MYMD1 1050mg cohort
Group V: Cohort 3: Placebo 900mgPlacebo Group1 Intervention
Subjects assigned to the 900mg placebo group
Group VI: Cohort 4: Placebo group 1050mgPlacebo Group1 Intervention
Subjects assigned to the 1050mg placebo group
Group VII: Cohort 2: Placebo 750mgPlacebo Group1 Intervention
Subjects assigned to the 750mg placebo group
Group VIII: Cohort 1: Placebo 600mgPlacebo Group1 Intervention
Subjects assigned to the 600mg placebo group
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MYMD-1 900mg
2022
Completed Phase 2
~40
MYMD-1 750mg
2022
Completed Phase 2
~40
MYMD-1 600MG
2022
Completed Phase 2
~40

Find a Location

Who is running the clinical trial?

MyMD Pharmaceuticals, Inc.Lead Sponsor
2 Previous Clinical Trials
72 Total Patients Enrolled
Lon Lynn, DOPrincipal InvestigatorClinical Research of West Florida
Leonard Dunn, MDPrincipal InvestigatorClinical Research of West Florida
3 Previous Clinical Trials
1,743 Total Patients Enrolled
~11 spots leftby Nov 2025
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