A Phase 1 Clinical Trial of NTQ5082 in Healthy Volunteers

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

82

Participants

Timeline

Start Date

August 31, 2024

Primary Completion Date

December 31, 2024

Study Completion Date

February 28, 2025

Conditions
Complement-mediated Hemolytic Diseases
Interventions
DRUG

NTQ5082

single ascending dose, randomized, double-blind study,with 8 dose groups preset. The first cohort will be the sentinel group, consisted of 2 subjects receiving NTQ5082 capsules. The remaining cohorts required 8 subjects each, with 6 receiving NTQ5082 capsules and 2 receiving placebo.

DRUG

Placebo

multiple ascending dose, randomized, double-blind study,with 3 dose groups preset. All cohorts required 8 subjects each, with 6 receiving NTQ5082 capsules and 2 receiving placebo.

Trial Locations (1)

410035

The Third hospital of Changsha, Changsha

All Listed Sponsors
lead

Nanjing Chia-tai Tianqing Pharmaceutical

INDUSTRY