Shared manufacturing platform
All KNX programs use the same E. coli expression system and recombinant protein production process — manufacturing efficiencies scale across the entire pipeline.
The patented pAMP platform enables rapid deployment across disease indications — from precision prophylactic vaccines against high-consequence infectious diseases to multi-pathogen therapeutic candidates with no approved countermeasures.
| Program | Pathogen | Indication | Stage | Funding Pathway |
|---|---|---|---|---|
| KNX-001 | Andes Virus (ANDV) | Hantavirus Pulmonary Syndrome (HPS) | Preclinical | Prophylactic Vaccine |
| KNX-002 | Rift Valley Fever Virus (RVFV) | Rift Valley Fever (RVF) | Preclinical | Prophylactic Vaccine |
| KNX-003 | RVFV & Hantavirus | Multi-Pathogen Viral Therapeutic | Discovery | Standalone Therapeutic |
| KNX-004 | RVFV & Hantavirus | Preventive / Therapeutic Combination Vaccine | Concept | Under Discussion |
Swipe the table horizontally to see all columns.
HPS is a severe respiratory illness caused by New World hantaviruses, of which Andes virus (ANDV) is among the most consequential. There are no approved vaccines or therapeutics, and the reported case fatality rate is 35–40%.
The 2026 multi-country Andes hantavirus outbreak aboard the MV Hondius cruise ship, declared by WHO, further underscores the urgent and active public health threat posed by ANDV, an agent posing high risk due to its potential for dissemination, high mortality, and lack of approved countermeasures.
Kinexar's pAMP-based HPS vaccine candidate is designed to elicit broad neutralizing antibody and T-cell responses, combining multi-epitope coverage with a thermostable, non-replicating format suited to national stockpiling.
Rift Valley Fever Virus (RVFV) is a Category A/B priority pathogen causing severe hemorrhagic fever in humans and catastrophic livestock losses. No licensed human vaccine exists. The 2025–2026 Senegal outbreak and WHO designation as a priority pathogen for pandemic preparedness underscore the urgency.
KNX-002 applies the patented pAMP platform to RVFV Gn/Gc glycoprotein epitopes, targeting the same neutralizing antibody response that confers protection in natural infection. A single platform approach enables parallel development alongside KNX-001 with shared manufacturing infrastructure.
KNX-003 is a pAMP-based antiviral therapeutic candidate targeting a conserved viral virulence factor shared across both RVFV and hantaviruses. The target plays a key role in immune evasion, and no approved therapeutic against it exists for either pathogen.
By leveraging the patented pAMP platform's concatemeric architecture, KNX-003 is designed to engage its target with multi-valent binding, restoring host immune competence. Because the target is conserved across both pathogen families, a single KNX-003 candidate addresses both RVFV and hantavirus — a cross-pathogen therapeutic with no equivalent in development.
KNX-004 is a concept-stage program exploring the combination of pAMP-based prophylactic antigen immunization (KNX-001/KNX-002) with the antiviral therapeutic component (KNX-003) into a single preventive/therapeutic vaccine candidate.
Such a combination would offer both pre-exposure protection and post-exposure therapeutic benefit in a single administration — a format with no precedent for either hantavirus or RVFV. The concept leverages the patented pAMP platform's modularity: combining prophylactic and therapeutic concatemeric components requires no change in manufacturing platform or delivery format.
KNX-004 is under active scientific discussion. No formal development decision has been made.
All four KNX programs share the same manufacturing platform, the same expression system, and the same regulatory pathway — compressing timelines and cost across the entire pipeline.
All KNX programs use the same E. coli expression system and recombinant protein production process — manufacturing efficiencies scale across the entire pipeline.
Thermostable, non-replicating constructs reduce cold-chain burden, supporting national stockpile and field-deployment scenarios across all programs.
Standard recombinant protein production avoids live-virus handling and specialized containment infrastructure, enabling scale-up without BSL-3/4 manufacturing facilities.
The patented pAMP platform is modular across modalities — the same platform that builds prophylactic vaccine antigens also polymerizes therapeutic inhibitor peptides, enabling both product types from one technology base.
New pathogen programs are initiated by designing epitope concatemers against the target — no new platform, no new delivery system, no new manufacturing process.
KNX-003 targets a conserved viral virulence factor across both RVFV and hantavirus — a single therapeutic candidate addressing multiple high-priority pathogens simultaneously.
Contact us for program details, preclinical plans, and collaboration opportunities across the KNX pipeline and the pAMP platform.