Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This investigational combination regimen, developed by Northwestern University's Comprehensive Transplant Center, is designed to induce immunologic tolerance in HLA-identical sibling kidney transplant recipients. The protocol utilizes alemtuzumab (Campath-1H), a monoclonal antibody targeting the CD52 antigen, as an induction agent to deplete host lymphocytes and monocytes. This is followed by infusions of purified donor CD34+ hematopoietic stem cells (DHSC) to establish cellular chimerism and donor-specific unresponsiveness. The ultimate goal of the regimen is to allow for the complete withdrawal of maintenance immunosuppressive therapy within 24 months post-transplant. Clinical trial results from NCT00619528 have demonstrated durable tolerance in a subset of patients, potentially eliminating the long-term side effects associated with chronic immunosuppression.
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 alemtuzumab + donor hematopoietic stem cells.