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Novo Nordisk Boosts Sickle Cell Disease Pipeline with IMMvention Collaboration

Marcus LeeWednesday, Jan 22, 2025 3:27 pm ET
3min read


Novo Nordisk A/S (NVO) has inked a strategic collaboration and license agreement with IMMvention Therapeutix, Inc. to co-develop oral therapies for sickle cell disease (SCD) and other chronic conditions. The partnership leverages IMMvention's investigational small-molecule BACH1 inhibitors, which have shown promise in preclinical studies. This collaboration strengthens Novo Nordisk's position in the SCD market and expands its pipeline of innovative therapies.

IMMvention's BACH1 inhibitors have the potential to increase fetal hemoglobin (HbF) expression, which is believed to ameliorate SCD disease pathology. The orally dosed inhibitors target BACH1, a key regulator of cellular responses, oxidative stress, and inflammation in multiple disease states. Under the agreement, Novo Nordisk gains an exclusive worldwide license to IMMvention's BACH1 program, with the companies working closely together to advance the inhibitors from preclinical development to development candidate nomination.

Upon or before the nomination of a development candidate, Novo Nordisk will take over all further development, regulatory submissions, and commercialization worldwide. Separate from the systemic BACH1 inhibitors that are part of the collaboration, IMMvention has retained rights to develop certain brain-penetrant BACH1 inhibitors, which could address diseases such as Parkinson's and Alzheimer's.



Novo Nordisk's expertise in rare diseases and global reach can significantly enhance the development and commercialization prospects of IMMvention's BACH1 inhibitors. The company's track record in developing and commercializing treatments for rare diseases, combined with its extensive global presence, enables it to conduct clinical trials in diverse populations and establish a robust supply chain and distribution network for commercializing the drug once approved.

IMMvention's timeline for IND-enabling studies and Phase 1 clinical trials in 2026/27 aligns with the competitive landscape in the SCD market. Other companies, such as Forma Therapeutics, are also advancing their therapies through clinical development. If IMMvention's BACH1 inhibitors demonstrate safety and efficacy in early-stage trials, they could potentially challenge other therapies in the market, depending on the results of Phase 3 trials.



In conclusion, Novo Nordisk's collaboration with IMMvention Therapeutix, Inc. strengthens its position in the SCD market and expands its pipeline of innovative therapies. The partnership leverages IMMvention's preclinical data on BACH1 inhibitors, which have shown potential in increasing fetal hemoglobin expression and ameliorating SCD disease pathology. With Novo Nordisk's expertise in rare diseases and global reach, the development and commercialization prospects of IMMvention's BACH1 inhibitors are significantly enhanced. As the competitive landscape in the SCD market continues to evolve, the success of IMMvention's BACH1 inhibitors will depend on their safety and efficacy in clinical trials.
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