introduction to analytical method development and validation for therapeutic proteins - sample...

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Analytical Method Development & Analytical Method Development & Validation for Therapeutic Proteins Validation for Therapeutic Proteins 1 Jichao (Jay) Kang, Ph.D., RAC Director, Analytical and Formulation Development Gallus Biopharmaceuticals NJ, LLC

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Training Seminar: Introduction to Analytical Method Development and Validation for Therapeutic Proteins Wednesday, January 21, 8:30 AM-4:25 PM - Thursday, January 22, 8:30 AM-12:30 PM Part of PepTalk: The Protein Science Week This course is a panoramic review of analytical method development and validation for therapeutic proteins, including antibodies and enzymes. It is intended for scientists working on therapeutic proteins in AD, QC, PD or related functional areas. It starts with basic knowledge of work on therapeutic proteins: manufacturing of proteins drugs, regulatory affair knowledge and protein chemistry. It then discusses fundamentals and practical aspects of commonly used analytical methods for proteins, including methods for structure elucidation, glycan characterization, biophysical characterization, potency measurement, purity and impurity analyses. The course concludes with the strategy and common practice in method validation and method transfer, including regulatory compliance at different stages of product development, application of DOE and QbD. The course emphasizes practical applications, real-world examples and useful tips. For full details visit www.chi-peptalk.com/peptalk_content.aspx?id=140090&libID=140061

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Page 1: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Analytical Method Development & Analytical Method Development & Validation for Therapeutic ProteinsValidation for Therapeutic Proteins

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Jichao (Jay) Kang, Ph.D., RAC

Director, Analytical and Formulation Development

Gallus Biopharmaceuticals NJ, LLC

Page 2: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Course ObjectivesCourse Objectives

Basic scientific and industrial knowledge of working on proteins (including antibodies)

Get familiar with commonly used analytical methods: purpose, advantages, limits, pitfalls

Get familiar with Protein CharacterizationGet familiar with method validation and method

transfer: principle, common practice, and potential problems

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Page 3: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Basic Structure of MAbBasic Structure of MAb

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Page 4: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Major N-linked GlycansMajor N-linked Glycans

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Classified depending on the extent of processing:High mannose: lack Gal or GlcNAc at the end of antennaeComplex: GlcNAc after the Man at the antennaeHybrid: have both Man and Gal/GlcNac at end of the antennae

Hybrid and Complex types can have two or more branches, termed Bi-antennary, tri-antennary, or Tetra-antennary

Page 5: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Reduced CE-SDS of MAbReduced CE-SDS of MAb

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Page 6: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

SEC-HPLC-MALSSEC-HPLC-MALS

Three detector monitoring

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Page 7: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Hydroxylated Proline and Lysine by AAAHydroxylated Proline and Lysine by AAA

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Page 8: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Protein Structure Elucidation by MS/MSProtein Structure Elucidation by MS/MS

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Roepstorff Nomenclature Scheme

Page 9: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Secondary Structure by CDSecondary Structure by CD

9T Estey, J kang et al., Pharm Sci , 2006, 95: 1626–1639

Page 10: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Timing for Method Timing for Method Qualification/ValidationQualification/Validation

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Preclinical Clinical Commercial

Phase I Phase II Phase III

Method Development and Qualification

Qualification Validation Verification

Measurement defined

Scientifically Defendable

Ready for validation

Fully ValidatedMethod Transfer

Methods related to product safety require qualification even at phase IOther methods need to be validated prior to BLA, but by phase III, you should

have the methods that can be validated

Page 11: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Case Study: Binding Assay QualificationCase Study: Binding Assay Qualification

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x axis

1 10 100 1000 10000 100000

0

1

2

3

Parallel Line Analysis

4-P Fit: y = (A - D)/( 1 + (x/C)^B ) + D: A B C D Rel. Pot.

Standard (Standard: Concentration vs Mean... 0.0395 1.31 202 2.61 1

Sample3 (150%: Concentration vs MeanVal... 0.0395 1.31 127 2.61 1.59

Sample1 (50%: Concentration vs MeanValue) 0.0395 1.31 372 2.61 0.541

Sample2 (100%: Concentration vs MeanVal... 0.0395 1.31 200 2.61 1.01__________

Curve Fit Option - Fixed Weight Value

PLA (Std. Curve: Standard) Degrees of Freedom: parallel = 37 free = 28 non-parallel = 9

R^2 = 1 F-stat = 2.14 F-prob = 0.712

Binding ELISA curves at different level

Page 12: Introduction to Analytical Method Development and Validation for Therapeutic Proteins - Sample Slides

Quiz # 15Quiz # 15

For an identification method, what are the validation parameters?

How to determine if a method is stability-indicating?

How to determine LOQ?How to calculate method supported

specification (SS)?List three considerations in setting SSTList three method transfer pitfalls

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