Webinar
Optimizing Early Phase Clinical Trials to Minimize Risk and Improve Decision-Making
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April 21, 2026

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10:00am - 11:00am

(GMT-05:00)

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In today’s rapidly evolving drug development landscape, early-phase clinical trials face mounting pressures: rising costs, shifting regulatory frameworks, geopolitical uncertainties, and heightened investor scrutiny. Yet, these challenges also open the door to transformative opportunities and “out of the box” thinking.

This webinar will explore how sponsors and CRO partners can leverage innovative trial methodologies — including customized adaptive designs, hybrid approaches, and model informed drug development (MIDD)— to generate high-quality data faster, make more informed go/no go decisions, and safely accelerate molecule progression.

Key discussion points will include:

  • The changing landscape of early-phase trials: navigating cost pressures, regulatory shifts, and global uncertainties.
  • Adaptive and hybrid trial designs: understanding disease process and novel drug targets, consolidating phases, integrating healthy volunteers and patient populations, and enabling faster and safe proof‑of‑concept decisions. Foundational pillars for success: specialized expertise, flexible customized adaptive design strategies, global site access and tested recruitment infrastructure, and integrated delivery models.
  • Global site networks: how strategically placed, safe and experienced, therapeutically aligned sites enhance patient recruitment, efficiency, and quality. Seamless early‑phase to late-phase transition: ensuring continuity, preserving institutional knowledge, removing white space, and streamlining data ecosystems.

Three key take-aways

  • Understand how customized adaptive and hybrid trial designs can consolidate phases, integrate diverse populations, and enable faster, safer go/no‑go decisions.
  • Learn why specialized expertise, robust site networks, and advanced analytics are essential for navigating complex protocols and accelerating molecule advancement.
  • Recognize how a seamless early‑phase to late-phase delivery model preserves institutional knowledge, streamlines data ecosystems, and reduces downstream costs—ultimately bringing treatments to patients faster.

For more information and to register, click here.

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