Drug Development Flashcards

1
Q

Describe the 3 main stages of drug development.

A
  1. Drug discovery - candidate molecules chosen, high-throughput screening of large compound libraries, lead optimisation
  2. Preclinical development - non-human studies, toxicity testing, pharmacokinetic analysis of ADME, formulation
  3. Clinical development - volunteers and patients, efficacy testing, side-effects and potential dangers
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2
Q

Describe the 4 stages of the clinical development phase of drug development.

A
  • Phase I - safety and tolerability (maximum tolerated dose - MTD)
  • Phase II - small scale efficacy/placebo controlled trial
  • Phase III - large scale efficacy/randomised double-blinded trial
  • Phase IV - post-marketing surveillance - long-term side-effects and efficacy monitored
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3
Q

Explain the different types of angiogenesis, its normal functions and how it contributes to disease.

A

Developmental:

  • Developmental vasculogenesis - organ growth in embryo

Normal functions:

  • Normal angiogenesis - adult wound repair, placenta during pregnancy, cycling ovary

Disease:

  • Insufficient vessel growth - stroke, MI, ulcerative disorders, neurodegeneration
  • Excessive vessel growth - cancer, inflammatory disorders, pulmonary hypertension, blindness
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4
Q

Explain the processes involved in tumour hypoxia.

A
  • Hypoxia, < 1% O2, is a strong stimulus for tumour angiogenesis
  • Hypoxia increases with increasing distance from capillaries
  • Hypoxia activates transcription of genes involved in angiogenesis, tumour cell migration and metastasis
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5
Q

Name 2 specific examples of pathological angiogenesis.

A
  1. Kidney cancer/renal cell carcinoma - highly angiogenic and metastatic tumour
  2. Wet age-related macular degeneration (AMD) -due to excess VEGF and leaky blood vessels
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6
Q

Describe and explain the main processes involved in vascular endothelial growth factor (VEFG) signalling.

A
  • k
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7
Q

Describe the stages in the development of Avastin (bevacizumab).

A
  • A4.6.1 - mouse monoclonal antibody that binds to human VEGF
  • Humanisation of mouse antibody achieved by exchange of 6 complementarity determining regions (CDR) into human antibody scaffold
  • Resulting “bevacizumab” was a humanised anti-VEGF antibody suitable for human clinical trials
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8
Q

Explain the mechanism of action of Avastin.

A
  • Avastin used as a monoclonal antibody
  • Binds to VEGF and prevents VEGF from binding to vascular endothelial cell receptors
  • VEGF signalling is inhibited and angiogenesis is inhibited
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