Week 2 Flashcards

1
Q

What is a ‘fair test’ and how is it achieved? (8)

A
  • ‘Perfect experiment’
  • Only one variable is changed

Can be achieved by:

  • Randomisation
  • Double blinding
  • Controlled
  • Pre specificy data analysis
  • Analysing data before unblinding
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2
Q

What are the different phases in clinical trials? (8)

A

Phase 1: 50-200 healthy volunteers
- Safety, PK and PD

Phase 2: 100-400 patients with the target disease
- Safety, PK and PD, proof of concept

Phase 3: 100- 5000 patients with the target disease
- Efficacy, proof of concept, less PK and PD

Phase 4: 1000- 1M- Post marketing

  • Long term safety and efficacy in clinical practice
  • Comparison to existing treatment
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3
Q

What do the FINER and PICOT acronyms stand for and what do they mean? (2)

A
FINER: for a good research question
Feasible
Interesting
Novel
Ethical
Relevant
PICOT: to refine a research question
Population
Intervention
Control
Outcome
Time
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4
Q

What is the difference between a parallel and cross over study? (3)

A

Parallel:

  • Independent groups take different drugs
  • Unpaired

Cross over study:

  • Participants take the same treatments in a different sequence, may involve a washout period
  • Paired
  • Own control group
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5
Q

What do GCP, IB, IMPD and SmPC mean? (4)

A

GCP:
- Set of internationally recognised ethical and scientific quality requirements for clinical trials

IB:

  • Summary info of all preclinical and clinical data
  • PK/ PD
  • Toxicology
  • Safety

IMP dossier:
- Info about quality, manufacture and control of IMP

SmPC:

  • Legal document after licensing that contains all information on the drug
  • Mirrors IB
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6
Q

What are clinical trial registers and what are examples? (2)

A
  • Practice of documenting clinical trials before they are performed in a clinical trial registry
  • Combat publication bias and selective reporting

Examples:
EudraCT (EU)
ISRCTN register (international standard randomised controlled trial number) (UK)
Clinicaltrials.gov (USA)

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7
Q

What is a sponsor? (1)

A
  • Individual, companty, institution, organisation or group of organisations that take on responsibility for:
    Initiation, management, financing

Legal requirement

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8
Q

What is the difference between a chief investigator and principal investigator? (2)

A

Chief investigator:
- Overall responsibility for the conduct of the whole project in the UK

Principal investigator:
- Conduct of research at a research site

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