Unconjugated NSS-01
The lead preclinical candidate, with pancreatic and colorectal cancer as primary development priorities, supported by in vivo research and cell-based studies in additional solid tumors.
We welcome discussions about licensing, acquisition of the NSS-01 program, or co-development, with pancreatic and colorectal cancer as co-equal development priorities.
The product opportunity spans standalone drug development, evaluation as a potential replacement for irinotecan or topotecan in selected combinations, and exploration as an alternative topoisomerase I ADC payload.
License the NSS-01 program.
Acquire the NSS-01 program.
Develop the program together.
Licensing, sale of the NSS-01 program, and co-development are open transaction options. We welcome discussions about the structure that best supports the program’s next stage.
The lead preclinical candidate, with pancreatic and colorectal cancer as primary development priorities, supported by in vivo research and cell-based studies in additional solid tumors.
The proposed transaction includes synthesis and formulation development associated with the program.
Additional targeted-delivery research offers an exploratory development direction, separate from the unconjugated candidate’s efficacy evidence.
Pancreatic and colorectal cancer are co-equal priorities for NSS-01. Research in the presence of human serum albumin (HSA) is central to the program’s scientific rationale. The opportunity spans development of the drug itself, its potential role within combination regimens and its evaluation as a topoisomerase I ADC payload.
Advance unconjugated NSS-01 as a single-agent oncology candidate and evaluate its potential as an alternative to irinotecan or topotecan. Pancreatic and colorectal preclinical findings provide the research foundation.
Evaluate whether NSS-01 could replace the camptothecin-derived component of selected combination regimens, including approaches that use irinotecan or topotecan.
Evaluate NSS-01 as an alternative topoisomerase I payload for ADC programs that use this drug class, with suitability assessed for each antibody–linker–payload design.
The efficacy findings presented here concern unconjugated NSS-01.
Understand the candidate, the comparative findings and the current development priorities.
Download PowerPoint overview ↓Talk through your pancreatic and colorectal oncology priorities, development capabilities and interest in the program.
Discuss access to study protocols, group sizes, raw data, synthesis information and the IP package as appropriate.
For licensing, sale of the NSS-01 program, or co-development inquiries, contact Bryce directly.
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