Newsletter | July 1, 2025

07.01.25 -- 2 Ways To Overcome The Challenge Of Developing Neurological Rare Diseases Drugs

CLINICAL TRIAL TECHNOLOGY

2 Ways To Overcome The Challenge Of Developing Neurological Rare Diseases Drugs

Guest Column | By Bruce Leuchter, MD, CEO, GRIN Therapeutics, Clinical Leader

GRIN Therapeutics CEO Bruce Leuchter, MD, explores how integrating new business models and technological advances will be crucial to developing new treatments for rare neurological disorders.

Deriving Reliable Clinical Outcome Scores From Continuous DHT Data

White Paper | ActiGraph

DHT-derived endpoints, especially percentile-based metrics, hold promise for robust, scalable measurement in clinical trials—provided they're chosen statistically and with adherence in mind.

Solving Key eCOA Challenges Through Digital Trials—Proof Points!

Article | Medable

Medable has reached some important milestones and shares them in its end-of-year report. Check it out to see what game-changing results they've brought to their customers.

Feasibility Insights In NSCLC With EGFR Mutations

Datasheet | Anju Software

Discover how the sponsor of a NSCLC trial targeting EGFR mutations leveraged customizable simulation tools to forecast enrollment timelines, mitigate site-level risks, and more.

Transforming Medical Data Into Research Insights

Brochure | OpenClinica

Discover the efficiency and security of automated, precise source data capture.

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