Cyclodextrin and antibody-drug conjugate formulations
View Patent ↗Disclosed are formulations, including both liquid and lyophilized formulations, comprising a benzodiazepine antibody-drug conjugate (ADC) and a cyclodextrin. Also disclosed are methods of purifying mixtures comprising benzodiazepine antibody-drug conjugates and process drug-related impurities.
1. A pharmaceutically acceptable formulation comprised of
(a) benzodiazepine ADC having the structure of:
or a pharmaceutically acceptable salt thereof, wherein
Ab is a monoclonal antibody that specifically to an extracellular domain of human CD33, wherein
the monoclonal antibody is h2H16ec having a variable light chain sequence comprising the amino acid sequence set forth in SEQ ID NO: 3 and a variable heavy chain sequence comprising the amino acid sequence set forth in SEQ ID NO:4 engineered to have introduced cyteine residues at position 239 (EU index numbering);
S represents the sulfur atoms from the engineered cysteine residue;
subscript p, which represents the average number of conjugated drug-linker molecules per monoclonal antibody in the formulation, is about 2, wherein conjugation of the drug-linker molecules is to the sulfur atoms of the introduced cyteine residues; and
wherein the concentration of the benzodiazepine ADC ranges from 1.3 mg/mL to 3.1 mg/mL;
(b) no more that 0.1 μM of a benzodiazepine-related impurity having the structure of:
or a pharmaceutically acceptable salt thereof
(c) 6% w/v of a chemically modified cyclodextrin, wherein the chemically modified cyclodextrin is hydroxypropyl-β-cyclodextrin;
(d) a lyoprotectant, wherein the lyoproptectant is 6% w/v sucrose; and
(e) a diluent, wherein the diluent is 20 mM KPhos buffer at a pH of 7.3.