Medidata Study Experience
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How To Double High-Performing Site Count In A Priority Indication
3/13/2023
A top 10 biopharmaceutical company wanted to expand its site list in a priority indication and better understand how existing sites in their database performed. Find out what happened next.
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The State Of Black Participation In Clinical Trials
2/24/2023
The need to design trials enrolling more demographically diverse patients is widely recognized. Learn why implementing effective, sustainable, and scalable enrollment diversity strategies remains a challenge for biopharmaceutical companies.
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Intelligent Trials - Diversity
2/17/2023
Medidata AI’s Intelligent Trials solution provides insights that allow you to take action to improve study diversity during the planning stages.
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New Therapeutic And Diagnostic Avenues In Breast Cancer
1/24/2023
This podcast discusses an important metastatic breast cancer study that was recently published in the New England Journal of Medicine and presented at ASCO - the American Society of Clinical Oncology in June 2022.
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A New Avenue In Breast Cancer Therapeutics
1/23/2023
Clinical trial findings may have unlocked a groundbreaking opportunity for breast cancer patients: beneficial therapy for HER2-negative patients with HER2-directed antibody-drug conjugates.
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3 Data Linkage Use Cases To Future Proof Your Clinical Trials
12/20/2022
Discover why access to compelling and relevant evidence is crucial to drug development, safety monitoring, and improved patient outcomes.
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The Future Of Data Linkage In Clinical Trial Evidence Generation
12/20/2022
Explore key questions about the future of AI and data linkage in clinical trial evidence generation.
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Imunon Phase IB Ovarian Cancer Study Shows Strong Progression-Free Survival Treatment Effect Using A Synthetic Control Arm
12/8/2022
Explore how Imunon used a control arm among stage III/IV ovarian cancer patients in their clinical trial.
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A Mid-Sized Sponsor Increased Site Count By 50% In A Rare Disease Clinical Trial
12/8/2022
In this case study, explore how a mid-sized sponsor chose high-performing sites based on reliable data to set their trial up for success.
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Medicenna Gains Precedent-Setting FDA Approval
12/8/2022
Learn how Medicenna was able to leverage Synthetic Control Arm (SCA) to bolster Phase 2 findings and gain FDA approval to design a hybrid external control arm for their Phase 3 registrational trial.