Clinical-stage pharmaceutical company Cirius Therapeutics Incannounced on Tuesday a planning grant from the Gates Foundation to advance the development of CIR-0602K as a potential postpartum therapeutic for women with a history of gestational diabetes mellitus (GDM).
The company says that this planning grant can potentially inform a multi-stage development programme to generate scientific and clinical evidence supporting CIR-0602K for postpartum use in women who develop GDM during pregnancy. The initial grant supports a planning and preparation phase for examining potential exposure of CIR-0602K in breast milk, with the objective of enabling future clinical studies in women immediately postpartum, subject to outcomes and regulatory feedback.
Outputs from this planning phase will potentially inform the design, regulatory expectations and execution of subsequent clinical studies, including trials conducted in LMIC settings. As part of this planning phase, Cirius says that it will also work with Certara, a global company involved in model-informed drug development, bringing specialised expertise in maternal-foetal and lactation modelling. Using the Simcyp Simulator, Certara scientists can predict drug exposure in breastfeeding mothers and infants, populations that are historically under-represented in clinical research.
CIR-0602K is an orally administered MPC inhibitor that has been evaluated in multiple Phase 2 studies across cardiometabolic indications. If future studies demonstrate safety and efficacy in the postpartum setting, the therapy could offer a practical and scalable intervention to reduce progression to type 2 diabetes, kidney disease and other chronic metabolic diseases following GDM.
According to Cirius, the compound's profile may be particularly advantageous for use in resource-limited settings. Cirius has committed to managing all project outputs in alignment with the Gates Foundation's Global Access principles, ensuring early consideration of affordability, accessibility, and relevance for LMIC populations.
Tandem Diabetes Care receives CE mark for expanded automated insulin delivery indications in Europe
Lupin's Ranluspec (ranibizumab) injection receives US FDA approval
MiniMed expands Abbott partnership for dual glucose-ketone diabetes sensors
Samsung Bioepis launches OPUVIZ across Europe for ophthalmic conditions
Hims & Hers expands GLP-1 offering in Canada with generic semaglutide
Bayer's KERENDIA receives FDA priority review for type 1 diabetes and kidney disease treatment
Dexcom launches Dexcom Flex CGM system for Type 2 diabetes patients in Germany
Apotex announces commercial launch of Apo-Semaglutide Injection in Canada
Bayer to acquire Perfuse Therapeutics in USD2.45bn deal to expand ophthalmology pipeline