First-in-human, randomized, double-blind, placebo-controlled, dose escalation trial of the anti-herpes simplex virus monoclonal antibody HDIT101 in healthy volunteers

Antje Blank,Nicolas Hohmann, Marlen Dettmer, Anette Manka-Stuhlik,Gerd Mikus,Felicitas Stoll, Marlies Stützle-Schnetz, Daniel Thomas, Evelyn Exner, Beate Schmitt-Bormann,Torsten Schaller, Rico Laage,Oliver Schönborn-Kellenberger,Michaela Arndt,Walter E Haefeli,Jürgen Krauss

CTS-CLINICAL AND TRANSLATIONAL SCIENCE(2022)

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摘要
HDIT101 is a first-in-class humanized monoclonal antibody recognizing a conserved epitope in glycoprotein B, a target present on the surface of herpes simplex virus 1 (HSV-1) and HSV-2 particles as well as on virus-infected cells. This was a first-in-human, single-center, double-blind, placebo-controlled trial in 24 healthy volunteers, randomized 3:1 (placebo:active) in each of the six dose levels with escalating doses up to 12,150 mg HDIT101. HDIT101 was administered intravenously, to study safety, pharmacokinetics (PKs), and immunogenicity. HDIT101 was well-tolerated in all recipients and no serious or severe adverse events, no infusion-related reactions, and no events suggestive of dose limiting off-target toxicity occurred. The mean serum exposure (area under the curve from zero to infinity [AUC(0-infinity)]) of HDIT101 showed a linear increase from 4340 h*mu g/ml at a dose of 50 mg to 1,122,247 h*mu g/ml at a dose of 12,150 mg. No immunogenic effects following HDIT101 exposure were observed at any of the applied doses. HDIT101 demonstrated the expected PK properties of a monoclonal antibody was well-tolerated, and could be safely administered even at excessively high doses that may be required for treatment of patients with septical HSV spread.
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