Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a multi-agent conditioning regimen used primarily before allogeneic hematopoietic stem cell transplantation (HSCT), especially in patients with hematologic malignancies such as acute leukemia and lymphoid malignancies. The combination includes: - Fludarabine, a purine analog that inhibits DNA synthesis and has potent immunosuppressive properties. - Cytarabine (AraC), a pyrimidine nucleoside analog that interferes with DNA synthesis, mainly used for its antileukemic effects. - Busulfan, an alkylating agent that causes cross-linking of DNA strands leading to cell death; it is myeloablative and immunosuppressive. - Anti-thymocyte immunoglobulin (ATG), a polyclonal antibody preparation targeting human T cells, providing additional immunosuppression to prevent graft rejection and reduce the risk of graft-versus-host disease. This regimen aims to achieve sufficient myeloablation and immune suppression for successful engraftment while reducing toxicity compared to more intensive regimens. It is considered an intensified or reduced-intensity conditioning protocol depending on dosing[1][2][3][4].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on fludarabine + cytarabine + busulfan + anti-thymocyte immunoglobulin.