
Our Clinical Candidate VN-1032 is an orally-active, novel Selective Aryl Hydrocarbon Receptor Modulator
(SAhRM) with significant efficacy as immunotherapy in pancreatic and colorectal cancer.
VN-1032 reduces fibrosis and disease progression in pulmonary arterial hypertension (PAH) and chronic kidney disease (CKD).
Vasculonics chemical platform modulates a critical molecular pathway implicated across multiple disease indications, positioning VN-1032 as a potentially transformative treatment approach.
2020: Vasculonics Incorporated as C-Corp
2019-21: SBIR Phase I Award
A Novel Disease Modifying Therapy for Progression of Pulmonary Arterial Hypertension
2020-21: SBIR Phase I Award
A Potential DDAH-Biotherapeutic to Preserve Kidney Function in Cardiac Surgery Patients
2020-21: NHILB Catalyze Award
Preclinical Development of a Novel Disease Modifying Therapy for Pulmonary Arterial Hypertension
2021: BARDA Blue Knight QuickFire Winner.
A Novel Small Molecule DDAH Modulator for Treatment of Diabetic Kidney Disease
2021-23: NHILB Catalyze-2 Award
Preclinical Development of a Novel Disease Modifying Therapy for Pulmonary Arterial Hypertension
2024: SBIR Phase II Award
Development of a Novel Disease Modifying Oral Therapy for Pulmonary Arterial Hypertension
2026: Vasculonics obtains FDA response to Pre-IND briefing

Vasculonics is developing novel selective aryl hydrocarbon receptor modulators (SAhRM) to override immune suppression and cancer immune evasion.
•AhR stimulates IDO expression in cancer cells leading to generation of AhR activator Kyn.
•AhR induces PDL-1 and causes loss of effector function or exhaustion of CD8⁺ T-cells.
•AhR induces enrichment of Tregs in the tumor microenvironment which subsequently suppresses CD8+ T-cell proliferation and cytotoxicity.
•AhR modulates macrophage and dendritic cell activities.
Therefore, modulation of these AhR mediated immune suppressive activities by VN-1032 within the tumor microenvironment is a key strategy to enhance immunotherapy efficacy.



Vasculonics is developing novel selective aryl hydrocarbon receptor modulators (SAhRM) and suppressor of vascular toxin asymmetric dimethyl arginine (ADMA) the critical pathological mechanisms of PAH.
AhR is known to play important pathological roles in inflammatory and fibrotic diseases. AhR activation has been found essential for PAH progression in humans and animal models.
VN-1032 is a novel selective AhR modulator (SAhRM) that targets key mechanisms underlying inflammation, oxidative stress, and fibrosis, demonstrating disease-modifying efficacy in preclinical models of pulmonary arterial hypertension (PAH) and chronic kidney disease (CKD) when administered orally.

Jaipal Singh, PhD
CSO & Founder

Brad Lawson
CEO

Anantha Shekhar, MD, PhD
Co-Founder, SAB

Young Lee, PhD
Project Leader

Vijay Reddy, PhD, DABT
SVP, Toxicology

Raymond Kauffman, PhD
Pharmacology Advisor

Srinivas Kasibhatla, PhD
Chemistry Advisor

Hunter Gillies, MB ChB
Clinical Advisor

Douglas Balogh, PhD
FDA Regulatory Affairs / CMC Advisor

Robert Bacallao, MD
Chief Medical Advisor
1800 North Capitol Avenue, Noyes Pavilion 5th Floor, E504C, Indianapolis, Indiana 46202, United States