Therapeutic PD-1-antibody from the original Keytruda® commercial drug targeting the PD-1-antigen, also referred to as Keytruda® or pembrolizumab antibody. Research-relevant quantities are available as licence-free consumable in aliquoted or diluted variant. Therapeutic monoclonal antibodies can be used from researchers in in vitro and in vivo experiments, biosimilar developers can order different batches at the same time.

What our clients say

”Evidentic can supply different batches of reference products for precilinical research.The quick access to the on-stock batches allows for adhoc ordering, keeps costs down and makes a headstart possible!”

“Evidentic is a new source of cost-efficient therapeutic mAbs for our immonassays. And easy to order!”

“We develop innovative and biosimilar mAbs for a global market. Evidentic’s aRMPs are a great source of cost-efficient reference products for our research and development program.”

“Evidentic gives rapid access to originator biologics and different batches. For biosimilar developers and regulators, it will shorten the time to gauge the analytical acceptance range for multiple CQAs of biotherapeutics.”
pembrolizumab / Keytruda
Product Reference
Drug name | Keytruda® |
INN | Pembrolizumab |
API type | Pembrolizumab is a humanised monoclonal anti-programmed cell death-1 (PD-1) antibody(IgG4/kappa isotype with a stabilising sequence alteration in the Fc region) produced in Chinese hamster ovary cells by recombinant DNA technology |
Pharmacotherapeutic group | Antineoplastic agents, monoclonal antibodies |
ATC code | L01XC18 |
Target of antibody | PD-1; Synonyms: CD279, PD1, SLEB2, hPD-1, hPD-l, Ly101, Pdc1 |
General function | |
Short description | |
Pharmacodynamic properties (Mechanism of action; Source EMA document) | KEYTRUDA is a humanised monoclonal antibody which binds to the programmed cell death-1 (PD-1) receptor and blocks its interaction with ligands PD-L1 and PD-L2. The PD-1 receptor is a negative regulator of T-cell activity that has been shown to be involved in the control of T-cell immune responses. KEYTRUDA potentiates T-cell responses, including anti-tumour responses, through blockade of PD-1 binding to PD-L1 and PD-L2, which are expressed in antigen presenting cells and may be expressed by tumours or other cells in the tumour microenvironment. |
Pharmacodynamic properties (Pharmacodynamic effects; Source EMA document) | |
Original license holder | |
Marketing authorisation numbers | EU/1/15/1024/001 - 002 |
Marketing authorisation holder | Merck Sharp & Dohme Limited Hertford Road Hoddesdon Hertfordshire EN11 9BU United Kingdom |
Name of the manufacturer of the biological active substance | MedImmune, LL C Frederick Manufacturing Center (FMC) 633/636/660 Research Court Frederick MD 21703-8619, USA Boehringer Ingelheim (BIB) Pharma GmbH & Co. KG Birkendorfer Straße 65 88397 Biberach an der Riss Germany |
Name and address of the manufacturer(s) responsible for batch release | Schering-Plough Labo NV Industriepark 30, Heist-op-den-Berg B-2220, Belgium |
Max shelf life | 24 months |
Storage conditions | 2°C – 8°C |
List of excipients | L-histidine L-histidine hydrochloride monohydrate Sucrose Polysorbate 80 |