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Exam (elaborations)

CCRC Exam questions with answers

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  • CCRC
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  • CCRC

CCRC Exam questions with answers

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  • August 21, 2024
  • 10
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • CCRC
  • CCRC
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BravelRadon
CCRC Exam

Protocols - correct answer ✔✔1) General Information

2) Background info

3) Trial objectives and purpose

4) Trial design

5) Selection and withdrawal of subjects

6) Treatment of Subjects

7) Assessment of Efficacy

8) Assessment of Safety

9) Statistics

10) Source Data/Docs

11) Quality control/assurance

12) ethics

13) data handling and record keeping

14) financing and insurance

15) publication policy

16) supplements



Phase 1 - correct answer ✔✔-intro of new drug/investigational product into humans

-healthy population (exception: oncology and HIV)

-design: single dose, open label, max tolerated dose

-PR, PD, BA, BE, dosing, metabolis

*focus is SAFETY



Phase 2 - correct answer ✔✔-Intro to subjects with disease

-design: compare with placebo (exception: cancer and antibiotics), double blind

, *AIM: define dose

evaluate short term safety and efficacy in patients with disease

dose response, dose tolerance, AE's



Phase 3 - correct answer ✔✔-Evaluate overall benefit to risk in large group of patients

-broader eligibility, 2 or 3 tx groups. controlled or uncontrolled

*AIM: establish long-term safety and efficacy with selected doses in broad subject sample



dosing invervals, drug-drug interactions, risk-benefit

pivotal to FDA approval



Phase 4 - Post Marketing - correct answer ✔✔Continue to collect long-term safety data and gather
optimal use info

Conduct AFTER regulatory approves IND

Open label



IND - Investigational New Drug - correct answer ✔✔Application - FDA form 1571

Permit to perform research with a specific investigational new drug on humans for the first time in the
US

Includes: background info, rationale, sponsors plan

Continually amended by sponsors to reflect protocol changes and new info

Effective 30 days after receipt by FDA

Updated annually by sponsors



Documents/Filing Investigator Only - correct answer ✔✔1)Advertisement for subject recruitment

2) signed inform consent

3) source docs

4) subject enrollment logs

5) final report by investigator to IRB

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