Hematology

Develop Your Malignant & Classical Hematology Trials With Confidence

Address the complexities of malignant and classical hematology development with the expertise, scale and strategic support needed to accelerate programs and bring innovative therapies to patients. 

Expertise Across Hematologic Conditions

At IQVIA, we bring unmatched experience across the full spectrum of adult and pediatric hematology—from non-malignant disorders such as von Willebrand disease to aggressive blood cancers such as acute myeloid leukemia (AML), diffuse large B-cell lymphoma (DLBCL), and multiple myeloma. Our Hematology-Oncology Center of Excellence delivers deep scientific and operational expertise that accelerates clinical development and improves patient outcomes.

Accelerating Malignant Hematology Trials at Global Scale

310

Malignant Hematology trials conducted in the past 5 years

>45K

patients enrolled across 32 countries in the past 5 years

>20

Malignant Hematology indications have been supported in the past 5 years, including trials in Multiple Myeloma, Non-Hodgkin Lymphomas and Chronic Lymphocytic Leukemia

SOLUTIONS & INNOVATION

Advancing Hematology Development

End-to-End Trial Solutions

Overcome the operational and scientific challenges of hematology development with integrated solutions that connect strategy, study design, site activation, trial delivery and evidence generation across the development lifecycle.

Early Phase & Adaptive Innovation

Reduce uncertainty through adaptive trial designs, modeling and simulation, and data driven insights.

Regulatory & Dose Optimization Expertise

Navigate evolving regulatory expectations and dose optimization challenges with strategies designed to accelerate informed development decisions.

Disease-Specific Scientific Expertise

Address the scientific and operational challenges of developing treatments for complex hematologic diseases with expertise spanning multiple myeloma, AML, DLBCL, CLL, sickle cell disease and bone marrow failure syndromes, and more.

Accelerating Classical Hematology Trials at Global Scale

>150

Classical Hematology trials conducted in the past 5 years

>8,200

Patients enrolled across 81 countries in the past 5 years

>10

Indications supported in the past 5 years, including hemophilia, anemias, and immune thrombocytopenic purpura (ITP)

FACT SHEET
Your Hematology Oncology CRO Partner to Navigate Complexity with Confidence
Learn more about the expertise, scale and strategic support needed to navigate development complexity, accelerate programs and bring innovative therapies to patients faster.
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Therapeutic expertise — hands-on and hand-selected for biotech

Therapeutically aligned solutions to advance your clinical program to the next milestone.

Related solutions

Frequently asked questions

Browse answers to common questions about hematology clinical development.

Hematology trials often involve complex study designs, small or geographically dispersed patient populations, evolving regulatory expectations, and specialized endpoints. Sponsors may also face challenges related to biomarker strategies, dose optimization, patient recruitment, and coordinating global site networks. Successful development requires scientific, operational, and regulatory expertise tailored to each disease area.
Adaptive trial designs can help sponsors make more informed development decisions by incorporating emerging data throughout a study. In hematology, adaptive approaches may support dose optimization, improve study efficiency, and help address the complexities of rare diseases and novel therapies. When appropriately applied, these designs can reduce development risk while accelerating the path to meaningful clinical insights.
Sponsors need a strong CRO that supports clinical development across the full spectrum of malignant and classical hematology, from first-in-human and early-phase studies through global registration trials. IQVIA's experience spans all of this, including hematologic malignancies such as AML, multiple myeloma, DLBCL and CLL, as well as non-malignant conditions like sickle cell disease, hemophilia, and bone marrow failure syndromes.

By combining therapeutic expertise, adaptive trial design capabilities, modeling and simulation, regulatory guidance, and global operational support, sponsors canadvance early-phase hematology programs. Our teams work across malignant and classical hematology indications to support first-in-human studies, dose-finding strategies, patient recruitment, and efficient study execution.

Visit our web pages read thelatest oncology insights and learn more about our early phase clinical development expertise.