To Investigate the Safety and Efficacy of UB-421 Monotherapy in HIV Infected Adults

PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

June 30, 2015

Primary Completion Date

July 31, 2016

Study Completion Date

July 31, 2016

Conditions
HIV-1 Infection
Interventions
DRUG

UB-421

The UB-421 (dB4C7 mAb) will be supplied at a concentration of 10 mg/mL (100 mg in 10 mL vial). Subjects will receive 8 doses of the UB-421 by intravenous infusion at 10 mg/kg weekly (Cohort 1, 8 weeks) or 25 mg/kg bi-weekly (Cohort 2, 16 weeks).

Trial Locations (1)

11217

Taipei Veterans General Hospital, Taipei

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Taipei Veterans General Hospital, Taiwan

OTHER_GOV

collaborator

Kaohsiung Veterans General Hospital.

OTHER

collaborator

Kaohsiung Medical University Chung-Ho Memorial Hospital

OTHER

lead

United BioPharma

INDUSTRY