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What has the author Tom Brody written?
Tom Brody has written: 'Clinical trials' -- subject(s): Research Design, Clinical Trials Data Monitoring Committees, Drug Approval, Clinical Trials as Topic, Clinical trials, Drug approval
Does FDA regulate vaccines?
Yes, the FDA regulates vaccines to ensure their safety, efficacy, and quality. Vaccines must undergo rigorous testing in clinical trials before they can receive approval or emergency use authorization. The FDA reviews data from these trials and monitors vaccine manufacturing processes. Additionally, the FDA continues to oversee vaccines post-approval to ensure ongoing safety and effectiveness.
In the SCID-X1 gene therapy trials what problem later surfaced in three of the patients?
In the SCID-X1 gene therapy trials, three patients developed leukemia as a result of the treatment. This was due to the unexpected activation of an oncogene during the insertion of the corrective gene into the patients' cells.
Some doubted that Sacco and Vanzetti receive fair trials because they were?
immigrants.
What has the author Salah Abdel-aleem written?
Salah Abdel-aleem has written: 'The design and management of medical device clinical trials' -- subject(s): Medical instruments and apparatus, Clinical trials, Methods, Device Approval, Research, Equipment and Supplies, Clinical Trials as Topic
What is a controlled and uncontrolled trails?
Controlled trials are experiments in which one group receives a treatment while another group, the control group, does not. This design allows researchers to isolate the effects of the treatment and minimize the influence of external variables. Uncontrolled trials, on the other hand, do not have a control group, making it difficult to determine the treatment's effectiveness since all participants receive the intervention. As a result, conclusions drawn from uncontrolled trials may be less reliable.
What is the sequence of events for the approval of a medicine for human use?
laboratory testing (chemical or cell), animal testing, testing on healthy humans, clinical trials
What is the sequence of events in approval of a medicine for human use?
laboratory testing (chemical or cell), animal testing, testing on healthy humans, clinical trials
Is Dr Robert oldham doing research with CBT-1?
The research for CBT-1 has just completed phase III trials and is being reviewed for FDA approval. Dr Oldham was the primary researcher for this CBApharma investigation that should get approval.
How common is gene therapy?
Gene therapy is not practiced frequently. It is still in a clinical trial level. Though just temporary results are got often using gene therapy. In 2011 a person has been completely cured of hiv by gene therapy. But still it is a very difficult process since the man's entire bone marrow had to be removed and replaced!
How long was clinical trial before FDA approved Imitrex?
Imitrex (sumatriptan) underwent clinical trials for several years before receiving FDA approval in 1992. The trials included multiple phases to assess its safety and efficacy for treating migraines. While the exact duration of the clinical trial process can vary, it typically spans several years from initial research to final approval.
What happened to Mercy Lewis after the Salem Witch trials?
Along with the rest of the accusers, Mercy Lewis pretty much disappears from records after the trials so it is difficult to figure out her fate.
