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Exploring protease inhibitors as therapeutic agents
  • Background
  • What we're looking for
  • What we can offer you
  • Who we are
  • Q&A
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Get them answered by the team at Daiichi Sankyo.
Background

Proteases play a crucial role in maintaining health by regulating numerous physiological processes. The expression of protease is tightly controlled under normal conditions. However, dysregulation of protease activity can be a hallmark of various pathologies, including cancer, neurodegenerative diseases, and autoimmune disorders.  

 

Understanding the role of individual proteases in disease pathology is crucial for the development of therapies for protease-related diseases, particularly through the use of protease inhibitors. While progress has been made to develop protease inhibitors for therapeutic purposes, creating a potent and specific protease inhibitor is challenging. Lack of specificity can lead to off-target inhibition and may result in unexpected side-effects when used in humans.  

 

Daiichi-Sankyo established a proprietary platform for creating protease inhibitors that are highly potent and specific. We are seeking collaborations with researchers who have expertise in protease-related diseases, particularly those lacking effective treatments. In the collaborative research, we will create and provide inhibitors, and the collaborators are expected to advance the understanding of protease involvement in disease pathology and evaluate the therapeutic potential of protease inhibition.

What we're looking for

We are interested in diseases that can be treated effectively by inhibiting one or two proteases. The target protease(s) do not have to be expressed only extracellularly, but therapeutic efficacy must be expected by inhibiting the protease outside the cell. We are seeking research that 1) has identified key proteases, 2) needs inhibitors with high specificity to demonstrate the potential of the protease(s) as a therapeutic target, and 3) needs protease inhibitors with good pharmacokinetics that can be used in animal studies.

Solutions of interest include:
  • Researchers focused on diseases that could be treated by inhibiting one or two key proteases.
  • Cell-free and cell-based assays useful to understand pathophysiology.
  • Animal model of the target disease(s) (e.g. transgenic animal or knock-out animal).
Our must-have requirements are:
  • Reasonable expectation of dramatic improvement by single or dual protease inhibition.
  • Unlikely to cause harmful effects when inhibited, based on knockout animal studies and available literature.
  • Data from animal studies or cell experiments supporting the validity of targeting the protease(s).
Our nice-to-have's are:
  • Animal model of the target disease is available.
What's out of scope:
  • Diseases that require inhibition of three or more proteases for treatment
  • Diseases effectively treated by existing drugs (e.g., diabetes, hypertension, hyperlipidemia, and stomach ulcer)
  • Cancer
  • Infectious diseases
Acceptable technology readiness levels (TRL):
Levels 2-4
What we can offer you
Eligible partnership models:
Sponsored research
Benefits:
Sponsored Research
Funding is proposal dependent, with up to $ 100K/year for a 2-year project with potential follow-on funding for 1 year.
Who we are

At Daiichi Sankyo, we attach significant importance to working with academic institutions, startups and bioventure companies to discover new therapeutics in the place where hypotheses are brought and tested in order to expand possibilities for scientific innovation breakthrough. We build sustainable relationships with partner institutions and companies through open and fair alliance management and trust based on mutual respect as the foundation for effective collaborations. Our goal is to jointly create new value for patients by maximizing each other’s expertise and strengths.

https://www.daiichisankyo.com/rd/strategy_operations/open_innovation/

 Learn more
Reviewers
Q&A with Daiichi Sankyo

The Q&A is now closed.

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Q.
ADAM17 is a membrane-associated protease widely expressed in humans, responsible for releasing TNFα, IL-6R, EGF family members, and other substrates, playing a key role in various diseases. Interested in this protease?
2
Q.
We have developed inhibitors for Insulin Regulated Aminopeptidase that may have applications in treating fibrosis, is that of interest to you?
2
A.
Thank you for reaching out. We are committed to advancing research by providing inhibitors derived from our proprietary platform to researchers who need them. Best regards.
KS
Kousei Shimada, Director, Daiichi Sankyo
October 21, 2024
Is this response helpful?
0
0
Q.
Pls describe class of your protease inhibitors (small molecules, large molecule, peptide..?)
2
A.
Thank you for reachig out. Although detailed information cannot be disclosed, the target protease(s) do not have to be expressed only extracellularly, but therapeutic efficacy must be expected by inhibiting the protease outside the cell. Best regards.
KS
Kousei Shimada, Director, Daiichi Sankyo
October 21, 2024
Is this response helpful?
0
0
Q.
We may propose development protease Inhibitors as anticancer agents through pharmacophore, virtual screening followed by in vitro screening to suggest lead molecules by library screening of available chemical libraries.
1
A.
Thank you for your inquiry regarding the development of protease inhibitors as anticancer agents. While we appreciate your interest and the potential of this approach, we regret to inform you that our current focus does not include anticancer drug development. We wish you the best in your research and future endeavors. I hope this helps! If you need any further assistance, please let me know.
KS
Kousei Shimada, Director, Daiichi Sankyo
November 19, 2024
Is this response helpful?
0
0
Q.
A large market in the fertility field is genetic testing. This involves biopsying and embryo which liberates proteases and harms the embryo. Would you be interested in testing biocompatible proteases for IVF?
1
A.
Thank you for your inquiry regarding the Daiichi Sankyo proposals. Since we focus on "disease treatment by inhibiting specific proteases," we would like to confirm the following two points: ・Is your proposal is focused on obtaining inhibitors for proteases used in testing or diagnostics? ・Dose your proposal assumes the inhibition of one (or two) specific proteases? Thank you for your understanding.
KS
Kousei Shimada, Director, Daiichi Sankyo
November 20, 2024
Is this response helpful?
0
0
Q.
I lead projects to identify inhibitors of Human T-lymphocyte virus (HTLV), Bovine Leukosis Virus (BLV) and P. gingivalis by targeting the corresponding pathogens´ proteases. Would this be within the scope of this call?
1
A.
Thank you for reaching out. We have reviewed your inquiry regarding the project to identify inhibitors of Human T-lymphocyte virus (HTLV), Bovine Leukosis Virus (BLV), and P. gingivalis by targeting the corresponding pathogens' proteases. Unfortunately, this topic falls outside the scope of our current call. If you have any other questions or need further assistance, please feel free to contact us. Best regards,
KS
Kousei Shimada, Director, Daiichi Sankyo
October 11, 2024
Is this response helpful?
1
0
Q.
We are evaluating the role of degranulated neutrophil proteases in NET-triggered autoimmune diseases - in particular cathepsin G and elastase. Is this something of interest to you? Regards
1
A.
Thank you very much for your proposal regarding the role of degranulated neutrophil proteases, particularly cathepsin G and elastase, in NET-triggered autoimmune diseases. After careful consideration, we have concluded that it is difficult for us to proceed with your proposal at this time.
NG
Naoya Gotoh, Senior Researcher, Daiichi Sankyo
November 27, 2024
Is this response helpful?
0
0
Q.
We are developing RNAi tools and small molecules to inhibit cystatins. An imbalance between cystatins and cysteine proteinases has been associated with cancer and inflammatory diseases. Would this be within the scope?
1
A.
Thank you for your inquiry. We understand that you are developing RNAi tools and small molecules to inhibit cystatins. We are currently focusing on obtaining inhibitors for specific proteases that are responsible for the onset of diseases. If your objective is not to obtain inhibitors for a specific cysteine protease, it does not align with our scope.
KS
Kousei Shimada, Director, Daiichi Sankyo
November 7, 2024
Is this response helpful?
0
0
Q.
We are designing protease inhibitors for viral diseases (Dengue,JeV, SARS-Cov2). The process involves computational design of pharmacophore and virtual screening. Can you provide library of compounds for screening.
1
A.
Thank you for your inquiry. However, we regret to inform you that our current scope does not include infectious disease-related projects. We wish you the best of luck with your research and hope you find the resources you need.
KS
Kousei Shimada, Director, Daiichi Sankyo
November 7, 2024
Is this response helpful?
0
0
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