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Hematology

Patient-centric solutions for classical and malignant blood disorder trials

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Work with the experts in the design, conduct and management of hematology trials—from early phase to registrational and post approval.

Our experience matters

Advance your hematology therapy with our decades of experience working with large pharma, biotech and research organizations.

Advanced therapeutics expertise

Drive your trial forward with new cell and gene therapies, immuno-oncology drugs and protocols involving bone marrow transplantation.

A team approach

Work with a diverse team to aid in the design and execution of your trial, using our global network of oncologists, hematologists and trial delivery experts.

Classical and malignant hematology 

Fortrea combines scientific expertise with trial design strategists and operational delivery experts in partnership with regulatory and recruitment specialists to craft a complete solution to help accelerate your trials. You can count on our team of over a dozen hematologists with expertise in immuno-oncology therapies, cell and gene therapies and targeted therapeutics such as antibody-drug conjugates. 

With recent and relevant experience in classical and malignant hematology trials from early phase to registrational, including acute myeloid leukemia, paroxysmal nocturnal hemoglobinuria, multiple myeloma, thalassemia, non-Hodgkin and B-cell lymphomas, hemophilia and many more, we have the know-how to advance your hematology development needs.
 

Hematology experience that matters 

In the last 5 years, we have supported:

488 Studies
11k+ Sites
45k+ Patients

Top indications

Strategies and solutions that make a difference

Beyond our novel solutions, industry-leading processes and subject matter expertise for your hematology trial, you can:

  • Enhance site selection and maximize patient recruitment with Xcellerate®. Utilizing trial data with extensive central laboratory data and other data sources, we help enhance your hematology trial enrollment and retention, which is particularly important for rare hematological indications 
  • Train and qualify sites in your protocol procedures with close collaboration with core and specialty labs 
  • Benefit from adjudication that results in more robust data for DMC/DSMB safety reviews—and no delays to database lock—with Endpoint “fast track strategies”