Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD38-SADA:177Lu-DOTA is an investigational two-step pretargeted radioimmunotherapy designed for the treatment of relapsed or refractory non-Hodgkin lymphoma (NHL). The therapy uses a bispecific fusion protein, CD38-SADA, which tightly binds to the cell surface antigen CD38 and to radionuclides chelated to DOTA (tetraxetan). The SADA platform enables self-assembly into tetramers that have high avidity for tumor-associated CD38. In the first step, non-radiolabeled-CD38-SADA tetramers are administered and bind selectively to tumors expressing CD38; unbound protein disassembles into monomers cleared by the kidneys. In the second step, a radiolabeled payload (^177Lu chelated by DOTA) is infused and binds specifically to tumor-localized SADA proteins, delivering targeted irradiation while minimizing off-target toxicity. This approach aims for improved efficacy and safety compared to conventional radioimmunotherapies. The drug is being developed by Y-mAbs Therapeutics[1][3][4][5][6].
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 CD38-SADA:177Lu-DOTA.