LivingGLP1
Study S002415

A Phase 1 Study to Evaluate the Effect of Rifampin on the Pharmacokinetics of MDR-001 and the Effect of Itraconazole on the Pharmacokinetics of MDR-001 in Healthy Adult Study Participants

Registration

Registration
NCT07550621
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
28
Start
2026-05-06
Primary completion
2026-05-31
Lead sponsor
MindRank AI Ltd
Conditions
Healthy Volunteers (HV)
Interventions
DRUG:MDR-001; DRUG:Rifampin; DRUG:Itraconazole
Results posted
FALSE

Registered primary outcomes

  • Cmax of MDR-001 [Baseline (Day 1 pre-dose) and up to 48 hours post-dose on Day 1 and on co-administration (Day 10 for Part A, Day 7 for Part B).]
  • AUC0-t of MDR-001 [Baseline (Day 1 pre-dose) and up to 48 hours post-dose on Day 1 and on co-administration (Day 10 for Part A, Day 7 for Part B).]
  • AUC0-∞ of MDR-001 [Baseline (Day 1 pre-dose) and up to 48 hours post-dose on Day 1 and on co-administration (Day 10 for Part A, Day 7 for Part B).]

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