The future of drug development starts with smarter early-phase trials. Moving from first-in-human (FIH) to proof-of-concept (POC) is a major milestone, and the foundation for innovation that transforms patient care.
In this webinar, the featured speaker will explore how adaptive study designs and strategic site choices can unlock new possibilities, enabling biotech leaders to accelerate breakthroughs and bring life-changing therapies to market faster. Join us to learn how integrating adaptive study designs can help eliminate unnecessary “white space” between milestones and aid progression from FIH to POC.
By integrating flexibility into trial design, sponsors can respond dynamically to emerging data, streamline decision-making and accelerate timelines without compromising scientific rigor. The speaker will also examine the role of strategically selected sites in complementing commercial Clinical Research Units (CRUs). These specialized sites bring unique capabilities — such as access to targeted patient populations and highly skilled teams — that enhance operational delivery and support complex protocols. This approach ensures that trials are not only faster but also more robust and representative.
Register for the webinar to learn how strategic site selection and adaptive study design can elevate the execution of Phase I/Ib trials.
Speaker
Aatir Butt, MS, CPM, Senior Director, Global Project Management, Clinical Pharmacology Services, Fortrea
Aatir Butt is a seasoned leader in clinical research with nearly 20 years of experience in project management across early-phase clinical development. Currently serving as Senior Director, Global Project Management at Fortrea (formerly Covance and Labcorp), Aatir leads strategic initiatives and operational delivery in Fortrea’s integrated delivery model for FIH to POC, driving innovation and client satisfaction.
Message PresenterWho Should Attend?
This webinar will appeal to:
- Biotech developers getting ready for First in Human / clinical development
- Companies with asset(s) late in toxicology seeking to be ready for what’s next
What You Will Learn
Attendees will:
- Learn how adaptive study designs can eliminate white space and accelerate the path from first-in-human (FIH) to proof-of-concept (POC)
- Discover how strategically selected sites can complement commercial Clinical Research Units (CRUs) with specialized teams and patient access to optimize operational delivery
- Gain insight into a flexible, integrated matrix model and global Phase I patient experience, supported by deep therapeutic expertise in complex indications such as endocrinology and metabolism, inflammatory diseases, neuroscience and rare diseases
Xtalks Partner
Fortrea
Fortrea is a leading global clinical research organization (CRO) with over 30 years of clinical research experience, providing comprehensive Phase I-IV trial management, clinical pharmacology, and consulting services across 20+ therapeutic areas. Evolved from Covance and Labcorp, Fortrea is built for biotech and biopharma, delivering agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions in about 100 countries. We combine scientific rigor and operational excellence with innovation to help bring therapies from pipeline to patient. Together, exceptional is possible. Learn more about us at www.fortrea.com and follow us on LinkedIn and X (formerly Twitter).
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