Obesity Featured Articles
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Crafting The Vision: Building A Strong Value Story For Biotechs
1/14/2026
Early-stage biotechs need more than science — they need a clear vision. Learn to craft a value story that shows differentiation, market potential, and patient impact to attract investors and partners.
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Big Futures For Emerging Biopharma: Navigating Biotech Hurdles
1/14/2026
Emerging biopharma drives agile, data-driven, patient-focused drug development. Discover how to overcome complexity, speed timelines, and thrive in a fast-changing healthcare landscape.
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Accelerating Parkinson's Disease Clinical Research Through CHDR's Monocentre Recruitment Capabilities
1/14/2026
Centralized PD trials reduce variability, accelerate enrolment, and enable genetic stratification for targeted therapies. This streamlined model delivers high-quality data and faster timelines, helping sponsors move confidently from early-phase research to late-stage development.
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Scout's Science-Based Targets Commitment: What Comes Next
1/14/2026
Explore the latest Science Based Targets initiative commitment, clarifying what has been approved, what remains in progress, and the steps required before emissions reduction targets can be validated.
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Confronting "Time Toxicity" In Global Oncology And Rare Disease Trials For Operational Excellence And Patient Retention
1/14/2026
Time is the only truly finite resource in a clinical trial. Consultant Leila Cupersmith discusses how sponsors can better design trials with a lower time burden to boost enrollment, retention, and overall operational excellence.
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From Lab To Launch: Navigating The Transition To Commercial Readiness
1/13/2026
Many clinical-stage companies start thinking about commercialization too late. FTI Consulting experts team up to provide guidance on getting started early.
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Navigating The Enrollment Bottleneck In Early Oncology Trials
1/12/2026
Slow oncology trial enrollment raises costs and delays progress. AI prescreening, patient-focused engagement, and early pharmacology studies help accelerate recruitment and optimize trial design.
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Working (Well) With Patient Advocates: The Sponsor POV
1/12/2026
Aeovian CEO Allison Hulme reflects on Aeovian Pharmaceuticals' partnership with the TSC Alliance and how it’s informed research and development of their first-in-class selective mTORC1 inhibitor.
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Virtual Reality Endpoints Improve Measurement Of Patients' Real-World Benefit
1/12/2026
Opus Genetics CEO George Magrath, MD, discusses how the company introduced virtual reality-enabled assessments and relied on digital endpoints to better measure participants’ vision changes.
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Working (Successfully) With Pharma: A PAG's Perspective
1/12/2026
TSC Alliance President and CEO Kari Rosbeck details the patient advocacy group's unique and fruitful relationship with Aeovian Pharmaceuticals in developing the company's first-in-class selective mTORC1 inhibitor for TSC-related refractory epilepsy.