All partnering requests
Small molecules and peptides or screening system for pancreatic ductal adenocarcinoma PDAC cells
  • Background
  • What we're looking for
  • What we can offer you
  • Who we are
  • Q&A
Have questions about this request?
Get them answered by the team at Daiichi Sankyo.
Background

Pancreatic ductal adenocarcinoma (PDAC) shows the lowest 5-year survival rate among all cancerous tumors.

For this reason, there is an urgent need to improve the overall survival with new chemical modalities as an alternative to antibody drug conjugates (ADCs) technology.

Antibody drug conjugates (ADCs) technology is not ideal for PDAC. ADCs technology enables us to deliver cytotoxic agents selectively to the tumors. However, in PDAC, the extracellular matrix becomes dense and abnormal, creating a physical barrier to the delivery of therapeutic agents, including large molecules like antibodies, to tumor cells.

Thus, Daiichi-Sankyo aims to develop novel chemical derivatives designed to exhibit high levels of TME penetration and selective internalization into pancreatic ductal adenocarcinoma cells.

What we're looking for

We are seeking novel chemical derivatives (small molecules or peptides) that can be internalized into a wide range of PDAC cells selectively. We are also interested in screening systems to identify our desired chemical products.

Solutions of interest include:
  • Small molecules or peptides that exhibit high levels of TME penetration and selective internalization into pancreatic ductal adenocarcinoma cells
  • Novel screening system to identify our desired chemical products.
Our must-have requirements are:
  • in vitro data exhibiting the PDAC cell-selective internalization activity of the compounds or peptides
Our nice-to-have's are:
  • in vitro data is required, but it would be preferred to have animal/in vivo data as well.
What's out of scope:
  • The compounds or peptides that show specific cell killing activity in PDAC cells without selective internalization activity into the cells are out of scope.
Acceptable technology readiness levels (TRL):
Levels 3-5
What we can offer you
Eligible partnership models:
LicensingSponsored researchCo-development
Benefits:
Sponsored Research
Funding is proposal dependent, with up to $ 150K for 12 month 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.

Sort by:
Q.
Would you consider nanocarrier mediated drug delivery to targeted region under this project scope?
1
A.
Dear Muhammad, Thank you for your question. We are afraid that nanocarrier would be out of scope. Small molecules and peptides would be preferable. Best regards, Masashi
MN
Masashi Numata, senior researcher, Daiichi Sankyo
February 2, 2024
Is this response helpful?
0
0
Q.
I have two independent solutions in relation to the call. 1. Small molecules that exhibit high efficacy in killing PDAC cells. Available test data on human organotypic PDAC tissue culture. 2. A unique screening platform. Are these of interest?
1
A.
We are interested in the small molecules that exhibit PDAC cell or TME-selective internalization activity, but not cell killing activity. A unique screening platform which can evaluate the selective internalization activity of small molecules or peptides into PDAC cell or TME could be interesting for us.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 5, 2024
Is this response helpful?
1
0
Q.
Would screening for early disease detection be in scope?
1
A.
We are afraid that any screening for early disease detection would be out of focus.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 5, 2024
Is this response helpful?
0
0
Q.
Is the PDAC selective small molecule-drug conjugate (SMDCs) and related screening method under this project scope? if so, do you have preferred or recommended PDAC surface antigens for small molecule to recognize?
1
A.
Yes, we are interested in PDAC selective SMDCs and related screening method. We have no preference about the target.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 6, 2024
Is this response helpful?
0
0
Q.
We are working to develop a peptide-based drug for PDAC by using cell lines and tissues isolated from patients. The peptide targetable receptor over-expresses in PDAC & internalises, is it of interest to you?
1
A.
If your peptide can be internalized into PDAC cells selectively through the overexpressed receptor, it would be interesting for us.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 15, 2024
Is this response helpful?
0
0
Q.
Would analytical techniques, such as LC-MS/MS, fall within the scope of screening solutions of interest?
1
A.
No, it would be out of scope.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 18, 2024
Is this response helpful?
0
0
Q.
We are working on the characterization of small molecules targeting transcription factor dimerization for glioblastoma using live-cell fluorescence microscopy/spectroscopy. Is it within the scope for the methodology?
1
A.
We are afraid that it could be out of scope.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 27, 2024
Is this response helpful?
0
0
Q.
Hi, I specialize in molecular docking and in-silico studies, which are highly effective methods for screening optimal molecules for specific targets. If you're interested in collaborating, I can prepare a proposal. Best
1
A.
We are afraid that it could be out of scope.
MN
Masashi Numata, senior researcher, Daiichi Sankyo
March 27, 2024
Is this response helpful?
0
0
Sign up to access the full partnering request.
View the details of this request and connect directly with corporate R&D teams at Fortune 500 companies.
Share partnering request
Complete
Refine recommendations
Is this request relevant to you?
Eligible partners
Academic researchersStartups
Seeking partners focused on
Analytical ChemistryBiochemistryBioinformaticsBiomolecular ProcessesBiopharmaceuticsBiophysicsCell BiologyCell Membrane TransportComputational BiologyComputational Chemistry
22 more

Halo home
Partner smarter. Move faster.
Get new partnering requests
delivered to your inbox.