Study of Safety, Tolerability, and Pharmacokinetics of INE963 in Healthy Participants

PHASE1TerminatedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

May 13, 2021

Primary Completion Date

November 24, 2022

Study Completion Date

November 24, 2022

Conditions
Healthy Volunteers
Interventions
DRUG

INE 963

Part A: Single ascending dose with 7 planned cohorts\> Part B: multiple dose with 2 planned cohort q24x3 days

OTHER

Placebo

Part A: single ascending dose with 7 planned cohorts. Part B: multiple dose with 2 planned q24x3 days.

Trial Locations (1)

NG11 6JS

Novartis Investigative Site, Mere Way

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY