Abstract | AIMS: METHODS: A population pharmacokinetic model was developed based on data from the Phase II study and the Phase III studies OPERA I and OPERA II in patients with RMS. Data from the ORATORIO Phase III study in patients with PPMS became available after model finalization and was used for external model evaluation. RESULTS: The ocrelizumab serum concentration vs time course was accurately described by a 2-compartment model with time-dependent clearance. Body weight was found to be the main covariate. The area under the concentration-time curve over the dosing interval was estimated to be 26% higher for patients with RMS weighing <60 kg and 21% lower for patients weighing >90 kg when compared with the 60-90 kg group. The terminal half-life of ocrelizumab was estimated as 26 days. The extent of B-cell depletion in blood, as the pharmacodynamic marker, was greater with increasing ocrelizumab exposure. CONCLUSION: The pharmacokinetics of ocrelizumab was described with pharmacokinetic parameters typical for an immunoglobulin G1 monoclonal antibody, with body weight as the main covariate. The pharmacokinetics and B-cell depletion in blood were comparable across the RMS and PPMS trials, and the extent of blood B-cell depletion was greater with higher exposure.
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Authors | Ekaterina Gibiansky, Claire Petry, Francois Mercier, Andreas Günther, Ann Herman, Ludwig Kappos, Stephen Hauser, Yumi Yamamoto, Qing Wang, Fabian Model, Heidemarie Kletzl |
Journal | British journal of clinical pharmacology
(Br J Clin Pharmacol)
Vol. 87
Issue 6
Pg. 2511-2520
(06 2021)
ISSN: 1365-2125 [Electronic] England |
PMID | 33202059
(Publication Type: Clinical Trial, Phase II, Clinical Trial, Phase III, Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2020 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. |
Chemical References |
- Antibodies, Monoclonal, Humanized
- Immunologic Factors
- ocrelizumab
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Topics |
- Antibodies, Monoclonal, Humanized
- Humans
- Immunologic Factors
- Multiple Sclerosis
- Multiple Sclerosis, Chronic Progressive
(drug therapy)
- Multiple Sclerosis, Relapsing-Remitting
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