🇺🇸 FDA
Pipeline program

A first-in-human, randomized, double-blind, placebo-controlled, three-part study assessing the safety, tolerability, pharmacokinetics and pharmacodynamics of BP1.15205 after single and repeated oral ascending doses, including the BP1.15205 effect on cardiac repolarization, as well as an exploratory assessment of the food effect on the pharmacokinetics of BP1.15205 in healthy participants

P24-06

Phase 1 other active

Quick answer

A first-in-human, randomized, double-blind, placebo-controlled, three-part study assessing the safety, tolerability, pharmacokinetics and pharmacodynamics of BP1.15205 after single and repeated oral ascending doses, including the BP1.15205 effect on cardiac repolarization, as well as an exploratory assessment of the food effect on the pharmacokinetics of BP1.15205 in healthy participants for Narcolepsy is a Phase 1 program (other) at Bioprojet Pharma with 1 ClinicalTrials.gov record(s).

Program details

Company
Bioprojet Pharma
Indication
Narcolepsy
Phase
Phase 1
Modality
other
Status
active

Clinical trials