Pipeline

Precision Medicines to Transform Patient Lives

Our pipeline of therapeutics is being developed to specifically target the causative pathological mechanisms of a number of NETs-based diseases and beyond.

WARNING: Do NOT edit any of this Pipeline in this Designer Interface — only make changes to pipeline in the CMS. If you need a change that cannot be fixed in the CMS, contact lucia@sacdzn.com or steve@sacdzn.com

exDNASETM [DNASE1L3Candidates]
Indication
Discovery
Phase
IND-Enabling
EarlyClinical
Pivotal
Albumin-DNASE1L3
Fusion Protein
Phase
NTR-441 (prototype)
Albumin-DNASE1L3Fusion Protein
Systemic Lupus Erythematosus [With DNASE1L3 Deficiency]
NTR-1011 (lead)
Albumin-DNASE1L3Fusion Protein
Systemic Lupus Erythematosus
NTR-1011 (lead)
Albumin-DNASE1L3Fusion Protein
Rheumatoid Arthritis
DNASE1L3 Analog
Phase
NTR-641
DNASE1L3 Analog
Undisclosed

Our Approach

Neutrolis’ unique approach allows for detailed interrogation of NET-based diseases and development of first-in-class therapeutics.

Step One

Detailed mechanistic understanding of neutrophil diseases using proprietary humanized mouse models

Step Two

In silico and rational design of therapeutic candidates targeted to disease mechanisms

Step Three

Identification of genetically relevant patient populations using real-world evidence to enable the most efficient validation and characterization of clinical impact

Step Four

Rapid iterative prototyping and scalable manufacturing of lead molecules for clinical development

Step Five

Measurement of biomarkers for patient stratification and assessment of pharmacodynamic effects of therapeutic candidates 

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NET biomarkers drive precision therapies

Neutrolis systematically identifies biomarkers that provide high confidence in the selection, treatment and monitoring of patients that are candidates for Neutrolis’ therapies. We leverage real-world evidence, genetics, and biomarkers to clearly define populations at a genetic and physiological level. Neutrolis uses robust detection methods to select patients likely to respond to anti-NETs therapies. In addition to patient stratification, our pharmacodynamic biomarkers also allow us to monitor treatment response to our therapies.

1
NET fragments are released and circulate in the blood

In patients with inflammatory or autoimmune diseases, such as lupus, NETs are formed in tissues and organs. Due to low levels of intrinsic NET disassembly, small fragments of NETs circulate in the blood.

2
Identification of drug target exposure from patient's blood

Blood drawn and processed from patients will contain NET fragments, which are indicative of Neutrolis' drug target exposure.

3
Molecular analysis of NET fragments aid precision therapy

Molecular biomarker analysis on NET fragments provide additional insights into treatment strategies for patients.