Hematology
Malignant & Classical Hematology Trial Expertise
From first-in-human to global registration, IQVIA delivers end-to-end hematology expertise to accelerate innovation and improve patient outcomes worldwide.
From first-in-human to global registration, IQVIA delivers end-to-end hematology expertise to accelerate innovation and improve patient outcomes worldwide.
IQVIA is at the forefront of early-phase innovation in hematology, driving more intelligent and faster development across both malignant and classical conditions. Our teams apply adaptive trial designs, advanced modeling and simulation, and regulatory-aligned dose optimization to reduce risk and accelerate insights.
As part of our commitment to regulatory excellence, we align with FDA’s Project Optimus and Project FrontRunner initiatives, supporting more meaningful outcomes for patients.
From first-in-human studies in acute myeloid leukemia (AML), diffuse large B-cell lymphoma (DLBCL), multiple myeloma, and chronic lymphocytic leukemia (CLL) to complex trials in sickle cell disease and bone marrow failure syndromes, we combine scientific rigor with cutting-edge tools to deliver earlier answers and more efficient development pathways.
Therapeutically aligned solutions to advance your clinical program to the next milestone.
Access new resources for advanced therapy development, from candidate identification through market authorization.
Build on our experience of more than 245 rare disease studies in 96 countries to fulfill your promise of hope to millions around the world.
The right pediatric program to deliver your medicine sooner.
Unravel the complexities of cancer treatment with patient-level data-driven solutions.