Pipeline · Cardiometabolic

Atherosclerosis & Reversal.Phase II

HTN + atherosclerosis combined protocol — 28 compounds, 10 mechanisms M1–M10, 5-phase 24-week design with CAC (coronary artery calcium) primary endpoint. Includes the novel five-layer reversal hypothesis where Layer 3 (macrophage mineral resorption) is genuinely novel. PLAQUE-REVERSE trial design. 2nd provisional patent filed.

Status: Phase II
Therapeutic area: Cardiometabolic
Key: 28 compounds · PLAQUE-REVERSE · Patent #2

The mechanism we're betting on.

HTN + atherosclerosis combined protocol — 28 compounds, 10 mechanisms M1–M10, 5-phase 24-week design with CAC (coronary artery calcium) primary endpoint. Includes the novel five-layer reversal hypothesis where Layer 3 (macrophage mineral resorption) is genuinely novel. PLAQUE-REVERSE trial design. 2nd provisional patent filed. The full mechanism map — including compound list, dose escalation, pre-specified biomarker thresholds, and the cross-walk modifiers used when re-fitting blends from related indications — is part of the gated methodology pack.Gated

What the rest of the world is doing.

Numbers below are surfaced by Atlas Bio's ClinicalTrials.gov and PubMed RWE pipelines, run against the Atherosclerosis & Reversal indication. Counts are industry-wide trials registered on ClinicalTrials.gov, not Atlas Bio studies. Methodology →

RWE refreshed 2026-05-12
Phase I (B1/B2)
195
trials
Phase II (B3)
200
trials
Phase III (B4)
200
trials
Phase IV (B5)
200
trials

Locked before readout.

Predictions for this study are SHA-256 locked before any readout. Pre-registration covers target engagement, primary endpoint, secondary endpoints, and the falsification criterion. The hash, prediction wording, and timestamp are available to verified clinicians and indication researchers on request.Gated

Same stack, every indication.

Want the full Atherosclerosis & Reversal protocol?

The abstract above is open. Compound lists, dose escalations, SHA-256-locked prediction documents, agent-network reasoning chains, and trial design specifics are available to verified clinicians, indication researchers, and sponsors under MNDA. Contact management to begin the access request.

Contact management →