Pharmacokinetics and Preliminary Safety of Pod-Intravaginal Rings Delivering the Monoclonal Antibody VRC01-N for HIV Prophylaxis in a Macaque Model

Author:

Zhao Chunxia12,Gunawardana Manjula3,Villinger Francois12,Baum Marc M.3,Remedios-Chan Mariana4,Moench Thomas R.5,Zeitlin Larry6,Whaley Kevin J.6,Bohorov Ognian6,Smith Thomas J.4,Anderson Deborah J.7,Moss John A.3

Affiliation:

1. Emory University School of Medicine, Atlanta, Georgia, USA

2. Yerkes National Primate Research Center, Atlanta, Georgia, USA

3. Department of Chemistry, Oak Crest Institute of Science, Monrovia, California, USA

4. Auritec Pharmaceuticals, Inc., Pasadena, California, USA

5. ReProtect, Inc., Baltimore, Maryland, USA

6. Mapp Biopharmaceutical Inc., San Diego, California, USA

7. Departments of Obstetrics/Gynecology, Microbiology, and Medicine, Boston University School of Medicine, Boston, Massachusetts, USA

Abstract

ABSTRACT The broadly neutralizing antibody (bNAb) VRC01, capable of neutralizing 91% of known human immunodeficiency virus type 1 (HIV-1) isolates in vitro , is a promising candidate microbicide for preventing sexual HIV infection when administered topically to the vagina; however, accessibility to antibody-based prophylactic treatment by target populations in sub-Saharan Africa and other underdeveloped regions may be limited by the high cost of conventionally produced antibodies and the limited capacity to manufacture such antibodies. Intravaginal rings of the pod design (pod-IVRs) delivering Nicotiana -manufactured VRC01 (VRC01-N) over a range of release rates have been developed. The pharmacokinetics and preliminary safety of VRC01-N pod-IVRs were evaluated in a rhesus macaque model. The devices sustained VRC01-N release for up to 21 days at controlled rates, with mean steady-state VRC01-N levels in vaginal fluids in the range of 10 2 to 10 3 μg g −1 being correlated with in vitro release rates. No adverse safety indications were observed. These findings indicate that pod-IVRs are promising devices for the delivery of the candidate topical microbicide VRC01-N against HIV-1 infection and merit further preclinical evaluation.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | NIH | NIH Office of the Director

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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