Logix Biosciences
Pre-clinical Pharmaceutical Platform

An Integrated Pharmaceutical Antibacterial & Antiviral Platform

Stage: Pre-clinical

Advancing proprietary, dual-action mechanisms engineered to neutralize viral transmission and overcome antimicrobial resistance at the molecular source.

20+ yrs

No observed evolutionary resistance across independent study

2

Parallel patented assets — botanical and synthetic

3

Expedited FDA pathways in play

WHO list

Multi-drug-resistant target pathogens

The opportunity

A global threat that conventional antibiotics are structurally unequipped to meet.

The World Health Organization ranks antimicrobial resistance among the leading global public health threats. Conventional antibiotics act on a single target site; pathogens inevitably select for resistance, and the pipeline of new mechanisms has stalled.

Logix approaches the problem at the molecular source. A single patented engine is structurally disruptive rather than site-specific, removing the single point of failure that resistance exploits, and extending the same mechanism to viral transmission and tissue repair.

The platform · LBX242

One patented engine.
Three therapeutic fronts.

LBX242 is a patented composition, treated as a proprietary engine rather than disclosed as a formula. Not a pipeline of unrelated molecules: one structurally disruptive composition, expressed across three modes of action.

Antibacterial 01

Resistant bacteria

A patented composition is structurally disruptive in a way pathogens cannot route around. No evolutionary resistance has been observed across two decades of independent study.

Antiviral 02

Viral transmission

The same composition acts against enveloped respiratory viruses at the point of entry, neutralizing transmission before infection takes hold.

Angiogenic 03

Tissue repair

Beyond defense, the composition promotes angiogenesis and supports a regenerative tissue-repair pathway, addressing the conditions required for healing.

Regulatory momentum

Two assets.
Two FDA pathways.

Two independently patented compositions — one botanical, one synthetic — multiply delivery options and de-risk capital across parallel pathways. Both express the same patented LBX242 composition.

Asset 01

Botanical matrix

LBX242

Composition
A patented botanical matrix.
Human use
Three decades of broad global human use of the natural composition from which LBX242 is derived.
FDA pathway
505(b)(1) botanical pathway, qualifying on prior human use.

Asset 02

Synthetic small molecule

LBX242

Composition
Synthetic LBX242 derivative, engineered for precision delivery.
Designation
QIDP under the GAIN Act — five additional years of exclusivity and Fast Track.
FDA pathway
LPAD pathway, scaling trial burden to a resistant population.

505(b)(1) / 505(b)(2)

Dual new-drug application routes

LPAD / GAIN Act

Limited-population and antimicrobial incentives

QIDP

Qualified Infectious Disease Product

Fast Track

Expedited FDA review

Institutional validation

Strategic agreement with Mayo Clinic.

Mayo Clinic

Partner

Independent Medical Advisory Board

Leadership

The people behind the platform.

Full leadership & advisory
Gavin Gear

Gavin Gear

Founder & Chief Executive Officer

Mark Morris

Mark Morris

Co-Founder & Chief Financial Officer

Dr. Marc Stevens

Dr. Marc Stevens

Orthopedic Surgeon, Chief Medical Officer

Brett Edmonds

Brett Edmonds

Co-Founder, Board Member

Gateway

Scientific, regulatory, and partnership inquiries.

Access to the clinical data deck, the executive summary, and mechanism-of-action briefings is provided to qualified parties under confidentiality.

Office
Monterey, California, United States

Submit an inquiry

A private inquiry, reviewed under confidentiality.