CelerisAI · Program 2 · Scientific & Commercial Overview

Your Heart Deserves a
Smarter Medicine

Millions of heart patients are running out of options — not because the heart can't be helped, but because today's drugs hit a wall. CelerisAI is breaking through it.

Next-Generation Cardiovascular Science
64M
People worldwide living with heart failure
5-Year Mortality ~50%
1.28B
Adults globally with high blood pressure
46% don't even know it
32M
HFpEF patients with zero effective therapies
The forgotten half of heart failure
57%
5-year survival in Pulmonary Arterial Hypertension
Despite best-in-class standard of care

Current Heart Drugs Are Running Out of Road

Think of your blood vessels like pipes carrying water. In a healthy heart, your body produces a natural molecule called Nitric Oxide (NO) — a built-in signal that tells your blood vessels to relax and widen, letting blood flow freely.

But in a failing heart, this Nitric Oxide supply dries up. And here's the critical problem: almost every drug used today relies on that Nitric Oxide signal to work. No signal, no effect.

It's like trying to boost a phone's Wi-Fi signal when the router itself is switched off. The problem isn't the phone — it's that the signal source is gone.

"Traditional therapeutics that rely on amplifying existing NO streams become physiologically useless as the disease progresses."

CelerisAI Clinical Overview

CelerisAI Bypasses the Broken Signal Entirely

Instead of trying to amplify a Nitric Oxide signal that no longer exists, CelerisAI's molecule goes directly to the heart of the problem — activating two key biological switches without needing Nitric Oxide at all.

🔵

Switch #1: The cGC Pathway

This pathway directly relaxes and widens blood vessels — reducing the strain on your heart without relying on any upstream signals.

Potent vasodilation even in a NO-depleted environment
Actively fights scarring and stiffening of heart tissue (anti-fibrosis)
Inhibits dangerous blood clots from forming
🟡

Switch #2: The cAMP Pathway

This pathway supercharges the heart's pumping and filling ability — completely independently of the adrenaline system, avoiding the dangerous side effects of older drugs.

Stronger heart contractions without increased oxygen demand
Better diastolic (filling) function — the core of HFpEF
Broad anti-inflammatory effects across the heart muscle

"By directly activating both pathways from within, the molecule operates at full efficacy even in low-NO, failing-heart environments — a first of its kind."

CelerisAI Mechanism Overview

Why Current Options Fall Short

Every existing drug checks some boxes. None checks all of them. CelerisAI is designed to be the first.

Drug / Therapy Sustained Effect NO-Independent Dual Pathway Safe Profile Heart Failure
Nitrates (nitroglycerin)
Loses effect in 24–48 hrs
sGC Stimulators (vericiguat)
Still needs some NO to work
~~ ~~~
PDE5 Inhibitors (sildenafil)
Not approved for heart failure
Hydralazine
Reflex tachycardia risk
~~ ~~~
CelerisAI Dual Activator
NO-independent · Dual pathway · Oral

A $70 Billion Market — and a Gap No One Has Filled

Three massive patient populations. Three conditions where current medicine is failing. One platform molecule designed to address all of them.

$35B
Heart Failure
(All Types)
$28B
Hypertension
$7B
Pulmonary Arterial
Hypertension (PAH)
Total Addressable Market
$70 Billion
No existing oral drug delivers sustained, NO-independent vasodilation with synergistic dual-pathway activation. CelerisAI is the first designed specifically to do so.

The Heart Failure Crisis Needs a
New Answer

CelerisAI is building that answer — a novel molecule designed from first principles to work where everything else has stopped working.

Connect with Dr. Raval +91 94085 72629