Kangpu Biopharmaceuticals announced today that China's National Medical Products Administration (NMPA) has approved the Investigational New Drug (IND) application for KPG-818, advancing the treatment landscape for relapsed/refractory multiple myeloma (RRMM).
Mechanism of Action and Drug Properties
KPG-818 represents a novel approach in multiple myeloma treatment as an oral molecular glue modulator of the E3 ubiquitin ligase complex CRL4-CRBN. The drug exhibits high binding affinity to cereblon (CRBN) and effectively triggers the degradation of Aiolos (IKZF3) and Ikaros (IKZF1), key zinc-finger transcription factors involved in B-cell development. This mechanism enables KPG-818 to deliver multiple therapeutic effects, including immunomodulation, anti-angiogenesis, and direct anti-tumor activity.
Promising Clinical Results
The completed Phase I clinical trial in the United States has yielded encouraging results for KPG-818 in treating various hematological tumors. The drug demonstrated favorable safety and tolerability profiles, along with promising pharmacokinetic characteristics. Notably, KPG-818 showed therapeutic potential in heavily pretreated RRMM patients who had previously undergone multiple lines of therapy, including:
- Two immunomodulatory drugs (lenalidomide and pomalidomide)
- At least one proteasome inhibitor (bortezomib, ixazomib, or carfilzomib)
- A CD38 monoclonal antibody (daratumumab or isatuximab)
Development Pipeline and Company Focus
Kangpu Biopharmaceuticals, a clinical-stage biotechnology company, continues to advance its robust pipeline of potential first-in-class and best-in-class drug candidates. The company leverages proprietary technology platforms, including NeoMIDES®, gDACs®, and X-SYNERGY®, to develop innovative therapeutics targeting solid tumors, hematologic malignancies, autoimmune diseases, and inflammatory disorders.
The IND approval in China marks a significant milestone in KPG-818's development program and represents an important step forward in addressing the unmet needs of multiple myeloma patients who have exhausted current treatment options.