A research trial is a carefully organized study testing how a new treatment or a new drug works on humans. Research experiments are also called clinical trials or clinical studies. “Clinical” because it takes place in the clinic or hospital, not in the laboratory. A clinical trial is laid out in a protocol, a 100-130-page detailed description of the trial.
All clinical trials in Britain must be approved in advance by the Medicines & Healthcare Products Regulatory Agency and by the Ethics Committee. Clinical trials take place in 4 phases. Members of the British Research Panel may be invited to participate in Phases 2, 3 and/or 4.
Phase 1: The first time the drug is tested on humans. Typically, on a small group of healthy individuals (20-80 people). Phase 1 examines the safety of the drug, how it decomposes in the body as well as its perceived effects and side effects.
Phase 2: The trials are performed on a group of patients suffering from the illness the drug is aimed for. Often100-300 people participate. The purpose of the study is to further investigate the effectiveness of the new drug and to determine the right dosage.
Phase 3: These trials include many patients with the relevant disease, from 500-10.000 people. The new drug is tested against existing products on the market. The treatment’s effect and dosage are tested and side effects monitored. Phase 3 trials often lasts 2-3 years. Depending on the results, the pharmaceutical company then submits an application for authorization to release the drug or treatment to market.
Phase 4: These trials take place after the drug or treatment has been on the market for a while. A significant number of people receive the product and investigations are conducted to see whether there are other risks, new uses for the product or very rare side effects.
Clinical research depends entirely on patient involvement when developing and testing new medications and new therapies. All drugs must be tested on humans before being released for general use.
There are 6 good reasons why you should participate in clinical research:
The British Research Panel is approved by the Data Inspection Agency and complies with the strictest requirements for data security and storage.
Yes, it will not cost you anything to be a member of the British Research Panel.
A clinical trial or study investigates how a new medicine or treatment works on humans. It looks for both the effects and any possible side effects. Clinical trials are conducted in 4 phases.
No, participation is always free and voluntary. All medication and examinations related to the study are free of charge.
Yes, you will always receive compensation for your travel expenses. In most cases, you will also receive compensation if a clinical visit or an examination is extended.
Yes, you may unsubscribe and leave the panel at any time. We will delete all of your information in our database.
Yes, you may change your mind and withdraw from the study at any time.
You will only hear from British Research Panel if a new research study matches your health profile and takes place at a clinic or hospital in your area.With your consent, we send you an email where you can read more about the study.
All studies are conducted at British hospitals and clinics. Specialized doctors and highly trained nurses are responsible for the treatment and examinations in the research facilities.
Most studies have a duration of 1-2 years. You may expect to go to the site 3-4 times to begin with for thorough examinations, followed by routine visits every 4 months. However, this depends on the particular study.
Placebo looks like medicine, but is an inactive product, often a calcium tablet. In studies, placebo is sometimes given to a small group of participants to exclude a false, positive effect that often occurs, when people receive special care and monitoring in a study. Neither doctor nor participant knows whether they are handling placebo or the active substance. This is called a double-blind study.