Steps followed in clinical trial research to obtain sufficient evidence that a process  
                     would be useful in medical treatment. 
          There are 5 phases of clinical trials:
          
 	- Phase 0:
 The first clinical trials done among people. They aim to learn how a drug is 
                processed in the body and how it affects the body. In these trials, a very small dose of a 
                drug is given to about 10 to 15 people.
- Phase I:
 Tests the safety of a drug in healthy volunteers or subjects with indications. The 
                 aim is to find the best dose of a new drug with the fewest side effects. The drug is tested in 
                 a small group of 15 to 30 patients. Low doses are given initially to a few patients, higher 
                 doses are given in others until desired effect is reached or undesirable effects seen.
- Phase II:
 Further assess safety of a drug in a large sample of patients. The study drug is tested 
                among patients with a specific cancer type and new combinations of drugs may be used.
- Phase III:
 Compare a new drug to the standard-of-care drug. These trials assess the side effects   
  of each drug and which drug works better. Phase III trials enroll 100 or more patients.
- Phase IV:
 Test new drugs approved by the FDA. It studies the side effects caused over time by 
  a new treatment after it has been approved and is on the market. The drug is tested in  
  several hundreds or thousands of patients. This allows for better research on short-lived and  
  long-lasting side effects and safety.