Drug intelligence / Profile preview

nelitolimod + anti-PD-1

Development stage
Unknown
Lead developer
TriSalus Life Sciences
Modality
MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Retrograde Venous Infusion
01

Overview

This investigational combination immunotherapy is being developed by TriSalus Life Sciences for the treatment of locally advanced pancreatic ductal adenocarcinoma (PDAC). The regimen consists of nelitolimod (formerly SD-101), a Class C Toll-like receptor 9 (TLR9) agonist, administered in combination with a systemic anti-PD-1 checkpoint inhibitor. A distinguishing feature of this therapy is the use of TriSalus' proprietary Pressure-Enabled Drug Delivery (PEDD) technology via Pancreatic Retrograde Venous Infusion (PRVI) to deliver nelitolimod directly to the tumor site. This regional delivery method is designed to overcome the high interstitial fluid pressure and immunosuppressive tumor microenvironment typical of pancreatic tumors, potentially enhancing the efficacy of the checkpoint blockade by activating the innate immune system and sensitizing the tumor to T-cell mediated attack.

Other names
SD-101 + anti-PD-1nelitolimod + PD-1 inhibitoranti-PD-1-TriSalus Life Sciences, Inc.-pancreatic ductal adenocarcinoma
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TLR9 (Toll-like receptor 9)

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