Cyclodextrin and antibody-drug conjugate formulations

Patent metadata

Field	Value
Publication number	US-9610361-B2
Application number	US-201414774372-A
Country	US
Kind code	B2
Filing date	Mar 12, 2014
Priority date	Mar 13, 2013
Publication date	Apr 4, 2017
Grant date	Apr 4, 2017

Abstract

Disclosed are formulations, including both liquid and lyophilized formulations, comprising a benzodiazepine anti-body-drug conjugate (ADC) and a cyclodextrin. Also disclosed are methods of purifying mixtures comprising benzodiazepine anti-body-drug conjugates and process drug-related impurities.

First claim

What is claimed is:

1. A method for removing benzodiazepine drug-related impurities from a mixture comprising benzodizepine ADCs and benzodiazepine drug-related impurities comprising subjecting the mixture comprising benzodizepine ADCs and benzodiazepine drug-related impurities to tangential flow filtration while maintaining a concentration of at least about 1% w/v cyclodextrin in the mixture.

2. The method of claim 1 wherein the cyclodextrin is present in the mixture at the start of tangential flow filtration.

3. The method of claim 1 wherein the cyclodextrin is added to the mixture prior to any substantial removal of benzodiazepine drug-related impurities and cyclodextrin is thereafter maintained at a concentration of at least about 1% w/v in the mixture.

4. The method of claim 1 wherien the tangential flow filtration is constant volume diafiltration.

5. The method of claim 1 wherein tangential flow filtration is by a device comprising a pump, a filtration holder having an inlet, a filtrate outlet, a retentate outlet, an ultrafiltration membrane having a pore size of about 50 Kd or smaller that separates the filtration holder into an upstream compartment and a downstream compartment such that all filtrate must enter the inlet and pass through the ultrafiltration membrane before exiting the filtration holder through the filtrate outlet, a sample reservoir for holding the conjugation reaction mixture, and a buffer reservoir in fluid communication with the sample reservoir and wherein the buffer in the buffer reservoir comprises at least about 1% w/v cylodextrin, at least about 2% w/v cylodextrin, or at least about 3% w/v cylcodextrin.

6. The method of claim 5 wherein the buffer replaces the filtration volume at the same rate as the filtrate flow such that the volume in the tangential flow filtration device remains constant.

7. The method of claim 1 wherein the filtration is discontinuous diafiltration.

8. The method of claim 1 further comprising the steps of (i) contacting an antibody with a benzodizepine drug-linker under conditions sufficient to form a conjugation reaction mixture comprising benzodiazepine ADCs, and (ii) contacting the reaction mixture with a quenching agent to form a quenched conjugation reaction mixture, wherein said mixture subjected to tangential flow filtration is a quenched conjugation reaction mixture.

9. The method of claim 1 wherein the benzodiazepine drug-related impurities are quenched benzodiazepine drug-linkers.

10. The method of claim 9 wherein the quenched benzodiazepine drug-linkers have a SlogP value of no more than 7.50 or no more than 6.5.

11. The method of claim 1 wherein the benzodiazepine drug-related impurities are reduced to a level of about 1 μM or less, 0.5 μM or less, 0.1 μM or less, or 0.05 μM or less.

12. The method of claim 1 wherein the cyclodextrin is a chemically modified beta cyclodextrin selecting from the group consisting of hydroxypropyl beta cyclodextrin and sulfobutylether beta cyclodextrin.

13. The method of claim 1 wherein the benzodiazepine ADC is a monoclonal antibody conjugated to a pyrrolobenzodiazepine dimer, an indolinobenzodiazepine dimer or an oxazolidinobenzodiazepine dimer.

14. The method of claim 13 wherein the benzodiazepine ADC is a monoclonal antibody conjugated to a pyrrolobenzodiazepine dimer and having the following formula:

or a salt thereof, wherein Ab is a monoclonal antibody and p represents the average number of drug-linker molecules per antibody in the mixture and is about 2.

15. The method of claim 14 wherein the benzodiazepine drug-related impurity is a quenched drug-linker wherein the drug-linker prior to quenching has the formula:

or a salt thereof.

16. A liquid pharmaceutical formulation comprising:
a benzodiazepine ADC; and
cyclodextrin at a concentration of from about 3% w/v to about 30% w/v.

17. The liquid pharmaceutical formulation of claim 16 wherein the formulation further comprises at least one buffering agent; wherein the formulation is an aqueous solution and the concentration of that at least one buffering agent is effective to maintain a physiologically suitable pH.

18. The liquid pharmaceutical formulation of claim 16 , wherein the liquid formulation is an aqueous solution further comprising a lyoprotectant so that the aqeuous solution is suitable for lyophilization.

19. The liquid pharmaceutical formulation of claim 17 wherein the aqueous solution has a pH of about 6.0 to about 8.0.

20. The liquid pharmaceutical formulation of claim 17 wherein the at least one buffering agent in the aqueous solution is selected from the group consisting of Tris, acetate, histidine, citrate, phosphate, and succinate.

21. The liquid pharmaceutical formulation of claim 16 wherein the benzodiazepine ADC is present at a concentration of from about 0.5 mg/ml, 1 mg/ml or 2 mg/ml to about 10 mg/ml or about 30 mg/ml.

22. The liquid pharmaceutical formulation of claim 16 wherein the cyclodextrin is a chemically modified beta cyclodextrin selecting from the group consisting of hydroxypropyl beta cyclodextrin and sulfobutylether beta cyclodextrin.

23. The liquid pharmaceutical formulation of claim 16 wherein the benzodiazepine ADC is a monoclonal antibody conjugated to a pyrrolobenzodiazepine dimer, an indolinobenzodiazepine dimer or a oxazolidinobenzodiazepine dimer.

24. The liquid pharmaceutical formulation of claim 23 wherein the benzodiazepine ADC is a monoclonal antibody conjugated to a pyrrolobenzodiazepine dimer and the benzodiazepine ADC is as follows:

or a pharmaceutically acceptable salt thereof; wherein Ab is a monoclonal antibody and p represents the average number of drug-linker molecules per antibody in the formulation and is about 2.

25. The liquid pharmaceutical formulation of claim 16 wherein the antibody component of the benzodiazepine ADC is an antibody that specifically binds to a cancer cell antigen that is expressed on the surface of a cancer cell.

26. The liquid pharmaceutical formulation of claim 16 wherein the formulation is an aqueous solution having 0.1 μM or less benzodiazepine drug-related impurites.

27. The liquid pharmaceutical formulation of claim 16 wherein the formulation is an aqueous solution further comprising a lyoprotectant so that the aqeuous solution is suitable for lyophilization.

28. The liquid pharmaceutical formulation of claim 16 , wherein the formulation is an aqueous solution in which the benzodiazepine ADC is present at a concentration of from about 1 mg/mL to about 5 mg/mL.

29. The liquid pharmaceutical formulation of claim 28 wherein the benzodiazepine ADC in the aqueous solution is at a concentration of about 1 mg/ml, about 2 mg/mL or about 3 mg/mL.

30. The liquid pharmaceutical formulation of claim 16 wherein the formulation is an aqueous solution wherein cyclodextrin in the aqueous solution is at a concentration from about 6% w/v to about 10% w/v.

31. The liquid pharmaceutical formulation of claim 16 wherein the formulation is

Assignees

• Seattle Genetics Inc

Inventors

• Li Hui
• Jiang Shan
• Wallace Mary
• Meyer Damon

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61K9/19

  lyophilised {, i.e. freeze-dried, solutions or dispersions (lyophilised products with subsequent particle size reduction A61K9/14; granules or pellets made by lyphilisation A61K9/1682; solid oral dosage forms made by lyophilisation A61K9/2095; lyophilisation additives A61K47/00)} · CPC title

• B01D2315/16

  Diafiltration · CPC title

• A61K47/40

  Cyclodextrins; Derivatives thereof · CPC title

• A61K47/26

  Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin · CPC title