drugset / Trial / NCT01668043
Study to Evaluate Safety and Efficacy of UB-421 Antibody in HIV-1 Infected Adults
Phase 2
Completed
29 enrolled
United Biomedical
Kaohsiung Veterans General Hospital. · collabTaipei Veterans General Hospital, Taiwan · collabUBI Asia in Taiwan · collab
Non-randomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this Phase IIa study is to determine whether the antibody (UB-421), targeting the HIV-1 receptor on the CD4 molecule of T-lymphocytes and monocytes, is safe and effective when multiple doses are administered by intravenous infusion to asymptomatic HIV-1 infected adults and to assess pharmacokinetic parameters of the antibody in blood and on cells. The neutralizing activity of UB-421 blocks HIV-1 from binding to its receptor on CD4-positive cells; thus, UB-421 functions as an immunotherapeutic intervention to prevent HIV-1 infection.
Timeline
- Start
- 2012-09
- Primary completion
- 2014-03
- Completion
- 2014-03
Publications
- Background Wang CY, Sawyer LS, Murthy KK, Fang X, Walfield AM, Ye J, Wang JJ, Chen PD, Li ML, Salas MT, Shen M, Gauduin MC, Boyle RW, Koup RA, Montefiori DC, Mascola JR, Koff WC, Hanson CV. Postexposure immunoprophylaxis of primary isolates by an antibody to HIV receptor complex. Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10367-72. doi: 10.1073/pnas.96.18.10367.
- Background Lynn S and Wang CY. Designed deimmunied monoclonal antibodies for protection against HIV exposure and treatment of HIV infection. U.S. Patent No. 7,501,494. http://patft.uspto.gov/netahtml/PTO/srchnum.htm
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SEMZUVOLIMAB | Protein / enzyme biologic | 10 mg/kg | Intravenous |
| Subject | SEMZUVOLIMAB | Protein / enzyme biologic | 25 mg/kg | Intravenous |
Indications
No indication recorded.