Sumitomo Pharma America Inc (SMPA), a subsidiary of Japan-based Sumitomo Pharma Co Ltd, announced on Monday that it has signed a Cooperative Research and Development Agreement (CRADA) with the National Cancer Institute (NCI), part of the US National Institutes of Health (NIH).
The agreement is for the evaluation of enzomenib, an investigational, oral, small molecule designed to inhibit the menin and KMT2A protein interaction present in certain difficult to treat cancers.
The collaboration intends to harness the integrated expertise of SMPA and the NCI to further expand the scientific assessment of enzomenib as a potential therapeutic and explore additional cancers to deal with unmet patient requirements. Enzomenib will be explored in MyeloMATCH (Myeloid Malignancies Molecular Analysis for Therapy Choice), an NCI precision medicine clinical trial designed to improve treatment outcomes for individuals diagnosed with acute myeloid leukaemia (AML) or myelodysplastic syndromes (MDS). Enzomenib will also be explored with other important NCI programmes.
SMPA is currently evaluating enzomenib in Phase 1/2 clinical trials for relapsed or refractory acute leukaemia. It is designed to target the menin and mixed-lineage leukaemia protein interaction, a key interaction for acute leukaemia and other cancer cell growth. In preclinical studies, enzomenib demonstrated selective growth inhibition in human acute leukaemia cell lines with KMT2A (MLL) rearrangements or NPM1 mutations -- cancers with particularly high mortality rates and limited treatment options.
TransCode Therapeutics announces reverse stock split
Nutshell Therapeutics' NTS071 p53 allosteric reactivator cleared for US clinical trial
Blue Earth Therapeutics initiates Phase 2 trial in metastatic castrate resistant prostate cancer
TransCode Therapeutics reports progress in metastatic cancer trial
Ingenium Therapeutics' Gengleucel to enter Phase 2 trial in MRD+ AML following FDA feedback
AllyGPO and BioCareSD advance community oncology through integrated, tech-driven drug management
Nuformix receives positive EMA opinion for orphan drug designation of NXP002 in IPF
Atossa Therapeutics secures new US patent for proprietary (Z)-endoxifen formulations
Myosin Therapeutics receives grant to advance MT-110 clinical trial in methamphetamine use disorder
Bayer launches Phase I trial of targeted alpha therapy for advanced liver cancer
Oramed Pharmaceuticals invests in and collaborates with Alpha Tau Medical
House Rx launches AI-enabled pharmacy management platform
Avacta Therapeutics reports positive Phase 1 data for lead candidate
Portage Biotech advances PORT-7 to clinical trial after positive mesothelioma preclinical results