Focus on Patients
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Your Workbook To Create A Rare Disease Clinical Trial Strategy
11/9/2021
In the rare disease space, planning and creating a robust patient recruitment plan is essential. This will lay the foundation for the budget, tactics, and expectations that are needed. In this article, the author shares her three-step process that she implemented in her career and it can set you on a path toward success for clinical trial recruitment in rare disease.
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Rare Disease Clinical Trials: 3 Areas We Could Improve On
11/4/2021
Rare disease clinical trials pose unique and complex challenges. Small and geographically dispersed locations of treatment centers, disease heterogeneity, and incomplete disease natural history can complicate the process. However, there are actionable and tangible steps we can take to improve the process and enable development of innovative and meaningful therapies.
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The BRAAVE 2020 Study: Engaging Black American Communities In HIV Clinical Research
10/28/2021
Black Americans are disproportionately impacted by HIV and have the highest rates of new HIV infections every year compared to other racial groups in the U.S. This article shares Gilead Sciences' methodology for a Phase 3 clinical trial for engaging patients living with HIV who self-identified as Black, African American, or mixed race.
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Co-Creating With Patients: The New Guide To Expanded Access
10/12/2021
Recently, Janssen Pharmaceutical Companies had the privilege of working with patients and advocacy groups to co-create a resource about expanded access for patients and caregivers. This article shares that story and describes how patients will benefit from the resource.
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What Can Clinical Leaders Do To Tackle The Global Women’s Health Gap?
9/9/2021
Nearly 300,000 women die every year from preventable causes related to pregnancy and childbirth. Postpartum hemorrhage is the leading cause of maternal death globally — and in the US, it's on the rise. Uterine fibroids disproportionately impact Black women and are a leading cause of hysterectomies. We must drive a concerted, ecosystem-wide effort that scales up clinical research for women.
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Incorporating Patient Voice In Rare Disease Trials: 3 Lessons Learned
9/7/2021
As the rare disease market has expanded, being a patient-centered company has become a necessity as much as an aspiration. When we involve patients early on in our drug development programs, we get valuable insights and can understand their special situations, which helps us design the most effective solutions that meet their needs. Here are my three lessons learned.
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Tackling Health Misinformation Among Hispanics For Better Clinical Research & Patient Data
8/31/2021
For years, Hispanic communities have faced inequities in many aspects of healthcare — from finding health education, being health literate, accessing healthcare, and underrepresentation in clinical research. This article discusses CreakyJoints' efforts in tackling this health misinformation.
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2 Key Ways To Improve Patient Recruitment Of Minorities In Clinical Trials – A Participant’s Perspective
6/1/2021
John A. Reaves was compelled to participate in clinical trials for a COVID-19 vaccine. In this article, he discusses his experience and provides two recommendations, including potential strategies for accomplishing them, for how the industry can improve recruitment of minorities for clinical trials.
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Best Practices For Designing And Running Clinical Trials For Patients With Rare Diseases
5/25/2021
As an industry, we are constantly searching for ways to improve the drug development process – particularly in the rare disease space. One way to improve on running your rare disease clinical trial is to foster collaborative partnerships with patient advocacy organizations and to stay connected to patients throughout the trial. Here's how to do that.
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Incorporating The Voices Of Parents And Children In Pediatric Clinical Trials
3/9/2021
Pediatric trials are far more complex than simply evaluating a therapy in the context of a child’s disease or illness. They are a family affair that must accommodate the diverse needs of parents and other family members caring for those children. This article discusses recent survey findings from the Center for Information and Study on Clinical Research Participation.