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Examples of deficiencies in submitted data Drs. J. Welink Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 2 |2 | GCP overview Bioanalytical part Critical deviations in %
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 3 |3 | GCP overview Bioanalytical part Major deviations in %
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 4 |4 | Deficiencies Overall: no bio-study submitted insufficient clinical data Test and Reference product outside the 90% confidence intervals Inadequate validation method of the bioanalysis no submission of dissolution test study design outliers GLP/GCP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 5 |5 | Examples Subjects included: - subjects: normal healthy volunteers, male, 18-55 years * report all demographic data * report all withdrawals from study and reasons why * protocol: handling! Exclusion only when: - subject had vomited shortly after intake of product - analytical problem subjects
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 6 |6 | Examples subjects Case: Report stated that 32 subjects were selected and included in the study.
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 7 |7 | Examples subjects Case: Exclusion of subjects (1). - protocol 28 subjects enrolled - PK data 24 subjects used as defined by protocol - two drop-outs (for personal reason) - 26 subjects completed the study - selection procedure replacements not defined!! - replacements subjects 25 and 27
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 8 |8 | Examples subjects Case: Exclusion of subjects (1). Subject 26:
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 9 |9 | Examples - number of subjects: 36 - used for statistical analysis: 35 - reason: low drug plasma levels in one subject calculated 90% CI: AUC 0-t 0.83 – 1.07 C max 0.82 – 1.04 Conclusion: Bioequivalent! subjects Case: Exclusion of subjects (2).
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 10 | Examples subjects Case: Exclusion of subjects (2). subject excluded!
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 11 | Examples - number of subjects: 36 - used for statistical analysis: 36 calculated 90% CI: AUC 0-t 0.76 – 1.03 C max 0.79 – 1.02 Conclusion: not bioequivalent! subjects Case: Exclusion of subjects (2).
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 12 | Examples Blood sampling Adequate sampling times and period. - reliable estimation of Cmax - reliable estimation of extent of absorption (AUC) AUC 0-t / AUC inf > 80%
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 13 | Examples Case: sampling scheme. Drug: literature reported t max 2 – 7 hours Blood sampling
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 14 | Case: t max. Blood sampling
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 15 | Examples Elimination half-life
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 16 | Examples Reference product Case: manufacturer. Protocol : Study report:
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 17 | Examples Reference product Case: change manufacturing process. - normal crossover bioequivalence study - number of subjects 38 - Test: ethionamide 250 mg capsule - Reference: Trecator-SC 250 mg tablet - 90% CI: AUC 0-t 0.95 – 1.28 C max 1.02 – 1.51 Conclusion: Not bioequivalent!
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 18 | Examples Reference product Case: change manufacturing process.
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 19 | Examples Test product Case: formulation. Application: Studied:
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 20 | Examples - LOQ: 10 ng/ml, sampling period 96 hours - AUC 0-t : 639 +/- 258 ng.h/ml - AUC inf : 1367 +/- 379 ng.h/ml - C max : 31 +/- 14 ng/ml Analytical method Case: LOQ (1).
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 21 | Examples Case: LOQ (2). Analytical method
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 22 | Examples Specificity/selectivity: Analytical method
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 23 | Examples Case: stability (1). Analytical method
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 24 | Examples Case: stability (2). Case: stability (3). Analytical method
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 25 | Examples Results: Pharmacokinetic data - check PK results; also C-t curves - in line with to be expected - normal variability PK data
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 26 | Case: C max. PK data
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 27 | Examples Case: C-t curves. PK data
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 28 | Examples - number of subjects: 24 - used for statistical analysis: 24 - non-parametric testing - reason: non normal distribution calculated 90% CI: AUC inf 0.98 – 1.23 C max 0.99 – 1.24 Conclusion: Bioequivalent! Case: testing. Statistical analysis
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 29 | Examples Case: testing. Statistical analysis
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 30 | Examples Case: testing. - number of subjects: 24 - used for statistical analysis: 24 - parametric testing !!!!!!!!!! - reason: detection of an outlier considered not acceptable calculated 90% CI: AUC 0-t 0.98 – 1.23 C max 1.01 – 1.38 Conclusion: Not bioequivalent! non parametric testing considered not acceptable! Statistical analysis
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 31 | Examples GCP/GLP criteria local market ≠ world market GLP fraud original data/documents not available
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 32 | Examples Case: reanalysis statistical analysis could not confirm values obtained by applicant GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 33 | Examples Case: integration GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 34 | Examples Case: improper documentation GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 35 | Examples Case: manipulation GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 36 | Examples Case: manipulation GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 37 | Examples Case: manipulation GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 38 | Example Case: remarkable data GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 39 | Example Case: integration (1) GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 40 | Example Case: integration (2) GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 41 | Example Case: falsified data GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 42 | Example Case: falsified data GCP/GLP
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Workshop on WHO prequalification requirements for reproductive health medicines, Jakarta, October 2009 43 | End Thank you for your attention
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