Polatuzumab Vedotin drug aliquots can be used for in vitro or in vivo experiments. Several other reference drugs are also available.
The drug aliquots are generated by aliquoting (dividing and repackaging) the EU-licensed biosimilar drug.
Polatuzumab Vedotin drug aliquots can be used for in vitro or in vivo experiments. Several other reference drugs are also available.
The drug aliquots are generated by aliquoting (dividing and repackaging) the EU-licensed biosimilar drug.
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Up to 10 batches of original drugs for examining batch-to-batch variations
Up to 80% less compared to the original pharmaceutical price
Shipment within days worldwide according to GDP-standards
Up to 80% less compared to the original pharmaceutical price
Drug name | Polivy® |
INN | Polatuzumab Vedotin |
API type | ADC |
Pharmacotherapeutic group | Antineoplastic agents; other antineoplastic agents |
ATC code | L01FX14 |
Target of antibody | CD79b |
General function | |
Short description | Polatuzumab Vedotin is an antibody-drug conjugate composed of the anti-mitotic agent monomethyl auristatin E (MMAE) covalently conjugated to a CD79b-directed monoclonal antibody (recombinant humanized immunoglobulin G1 [IgG1]. |
Pharmacodynamic properties (Mechanism of action; Source EMA document) | Polatuzumab Vedotin is a CD79b-targeted antibody-drug conjugate that preferentially delivers a potent anti-mitotic agent (monomethyl auristatin E, or MMAE) to B-cells, which results in the killing of malignant B-cells. The Polatuzumab Vedotin molecule consists of MMAE covalently attached to a humanized immunoglobulin G1 monoclonal antibody via a cleavable linker. The monoclonal antibody binds with high affinity and selectivity to CD79b, a cell surface component of the B-cell receptor. |
Pharmacodynamic properties (Pharmacodynamic effects; Source EMA document) | Polatuzumab Vedotin did not prolong the mean QTc interval to any clinically relevant extent based on ECG data from two open-label studies in patients with previously treated B-cell malignancies at the recommended dosage. |
Original license holder | Roche Registration GmbH Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen Germany |
Marketing authorisation numbers | EU/1/19/1388/002 |
Marketing authorisation holder | Roche Registration GmbH Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen Germany |
Name of the manufacturer of the biological active substance | Lonza Ltd. Lonzastrasse CH-3930 Visp Switzerland |
Name and address of the manufacturer(s) responsible for batch release | Roche Pharma AG Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen Germany |
Max shelf life | 30 months |
Storage conditions | 2°C – 8°C |
List of excipients | Succinic acid Sodium hydroxide (for pH-adjustment) Sucrose Polysorbate 20 (E 432) |
Evidentic offers multiple batches of original drug aliquots in low binding Eppendorf tubes for research use only. We provide licence-free drug aliquots with long, short or even “negative shelf life” by storing the products at recommended temperatures (either 2-8°C or -80°C) and ensuring fully functional molecules for research purposes.
Evidentic GmbH
Am Mühlenberg 10
14476 Potsdam | Germany