A Phase 1 Study of the Safety and Tolerability of Single and Multiple Ascending Doses of BWC0977 in Healthy Volunteers

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

October 10, 2025

Primary Completion Date

June 30, 2026

Study Completion Date

August 30, 2026

Conditions
Infectious DiseasesAntimicrobial Drug Resistance
Interventions
DRUG

BWC0977

"SAD Cohorts: Double-blind dosing will occur. Six participants will receive single doses of BWC0977. The dose escalation steps may be altered following review of the safety data upon completion of each cohort.~MAD Cohorts: Double blind dosing will occur. Six participants in each cohort will receive multiple doses of BWC0977. The dose escalation steps may be altered following review of the safety data upon completion of each cohort. Dosing will commence on the morning of Day 1. Dosing frequency to be confirmed based on safety, tolerability, and PK data from SAD and previous MAD cohorts. Daily dosing will continue for a total of 7-10 consecutive days (as per schedule)."

DRUG

Placebo

SAD Cohorts: Two participants in each cohort will receive a matching placebo. MAD Cohorts: Two participants in each cohort will receive a matching placebo.

Trial Locations (1)

3004

Nucleus Network, Melbourne

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Nucleus Network Ltd

OTHER

lead

Bugworks Research Inc.

INDUSTRY