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Cancer Research

Cancer research and innovation

Clinical trials and research studies help evaluate a variety of factors related to a medication or treatment. These factors include safety, effectiveness, possible side effects, dosage measurement, and even if certain patients are more likely to respond to a treatment compared to others.

Every medication and treatment available today was, at some point, studied as part of a clinical trial. Without research, and the remarkable patients who choose to join these studies, innovative new treatment options like CAR-T and other immunotherapies would not be available today.

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​Cancer clinical trials

Baylor Scott & White Research Institute (BSWRI) conducts research exploring different cancer medications, therapies and care options. We support a wide variety of trials, across all phases, related to the following types of cancer:
  • Skin
  • Bone
  • Neurological
  • Breast​
  • Thoracic
  • Gastrointestinal
  • Gynecological
  • Head & Neck
  • Hematalogical (exs. leukemia, lymphoma, and multiple myeloma)
  • Genitourinary
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Enroll in a clinical trial

Learn about our actively enrolling cancer studies and contact us for more information

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Frequently asked questions

Why participate in a clinical trial?
What are the potential risks?
Because clinical trials and other research studies are designed to evaluate a new treatment or therapy, factors such as safety, side effects and basic effectiveness are a natural part of the evaluation. As such, participants may experience an adverse response or run the risk of the treatment or therapy having no effect at all. These factors are all discussed with patients in advance of any involvement, and patients are closely monitored throughout the process to watch for any such signs.
Am I guaranteed to get a drug or would I get a placebo?
Not all trials involve the use of a placebo. If the trial you are considering does involve placebos, a research team member will discuss this information and related details with you prior to as part of your initial screening.
What do I have to do to qualify?
Every research opportunity has specific inclusion and exclusion criteria that help determine if a person qualifies for the study. Research team members review these criteria with interested participants as part of an initial screening. Criteria can include general information like your age, as well as more detailed factors, such as the stage of cancer you have or other health conditions or procedures in your medical history. ​​​
What are the costs involved in a clinical trial?
Every trial is different, but generally participants do not have to pay for costs tied to the treatments or medications involved in the trial. These costs are generally covered by the trial’s sponsor(s). The patient (or the patient’s insurance provider) maintains the responsibility of covering costs related to any routine testing, procedures or medications they take as part of their existing cancer treatment.

As part of the trial, a BSWRI team member will review study consent forms with you and provide information about what payments you are and are not responsible for making.

Research participation can require more appointments, lab work, in-person visits, or even hospital stays than a participant is used to having. This is needed as part of the monitoring and study process, but may require more time investments than expected. Appointment and other study-related details will be discussed in advance with participants as part of the enrollment process.
Once I join a trial, am I required to stay enrolled?
No, you can stop participating in a clinical trial at any time and for any reason. You are not required to stay enrolled under any circumstances.
What are the different phases of research?
There are different types of studies and trials involved in research. Some focus on data collection and observation, or studying tissue and tumor samples. These types of studies generally require less time from the patient after samples and related information are initially captured. Others studies involve more direct patient interaction and monitoring – these are often the studies that involve evaluation of a new drug, or combination of drugs, or a new therapy or treatment approach. Below is a breakdown of these phases as explained by the U.S. Food and Drug Administration (FDA):

Phase 1: Studies that are usually conducted with healthy volunteers and that emphasize safety. The goal is to find out what the drug's most frequent and serious adverse events are and, often, how the drug is metabolized and excreted.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition). For example, participants receiving the drug may be compared with similar participants receiving a different treatment, usually an inactive substance (called a placebo) or a different drug. Safety continues to be evaluated, and short-term adverse events are studied.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing. These including post-market requirement and commitment studies that are required of or agreed to by the sponsor. These studies gather additional information about a drug's safety, efficacy, or optimal use.

Baylor Scott & White Research Institute currently supports research within each of the different phases and categories mentioned above. ​​​​​
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