Confidential
Confidential commercial, technical and financial material prepared for prospective institutional partners and investors — the layer we deliberately keep off the public site. Access is provided for evaluation only.
Access gate is for confidentiality acknowledgment · not a security control
Partner & investor dossier
The public site proves the science. This room covers what it can't: the pipeline detail, chemistry & manufacturing, regulatory roadmap, economics, deal terms, competitive position and risk — the package a partner or investor needs to act.
The full public evidence record (papers, patents, designations) lives on the site →01 — Evidence, in one line
The full, sourced record — every paper, patent and designation — is public on the site's Scientific Dossier. Here is the headline; the rest of this room is what's not public.
peer-reviewed papers
patents
US FDA orphan designations
years, one team
countries
02 — Pipeline detail
Each candidate adapts the same magnesium-stabilized antisense chemistry to a different target. Stages are shown honestly; per-candidate data packages are available on request.
02b — Real-world observations
Across the twenty candidate programs, clinicians at IMMUNIC have recorded individual, anonymized outcomes. These are observational, investigational, and not guaranteed — shared here for partner diligence only.
Cardiometabolic
Endocrine · Renal · GI
Oncology
Infectious
Autoimmune
Neurology · Psychiatry
Other
03 — Chemistry & manufacturing
The magnesium-chloride matrix is the proprietary core. Process, stability and unit economics are trade secrets shared with serious partners under NDA.
Composition & CMC
PK / PD & safety
04 — Regulatory roadmap
Two FDA orphan designations and an operational, Thai-FDA-registered IMMUNIC clinic (not a drug approval) anchor a staged path. Filing timelines are shared with partners.
IMMUNIC clinic operational
Antisense clinical-research center operating in Bangkok — investigational; no drug-approval claims
US FDA orphan track
V5 #457714 granted; V7 DRU-2019-7145 filed — pathway open
Pre-IND / IND (lead candidate)
Shared on requestFirst-in-human (Mg-ASO)
Shared on requestGlobal expansion (EMA / others)
Shared on request05 — Commercial & financials
A US public company has already licensed this lineage at commercial scale (Key Capital, 2020) — the model is de-risked. Round, valuation and projections are provided to qualified parties.
Financials
Licensing & deal terms
06 — Partnership terms
The institutional model in concrete terms — scope, support and economics defined per partner.
You receive
You lead
Commercials
07 — Competitive landscape
Antisense and siRNA are the proven modalities of the era — every approved player delivers by injection. Oral delivery is the open lane.
ASO market CAGR
industry estimates
Competitor properties from public literature; positioning is immugence's design rationale, not a head-to-head clinical claim.
08 — Risk register
Serious diligence expects an honest risk view. Here are ours and how we address them.
Clinical translation of Mg-ASO candidates
Builds on the lineage's published Phase II/III oral-immunotherapy results; staged, target-by-target validation.
Regulatory timeline & approval
Two FDA orphan designations already in hand/filed; honest staging — investigational, no approval claims.
“Too good to be true” perception
Evidence-led public site, third-party press (THE STANDARD), and verifiable PMIDs/patents/designations.
Manufacturing scale-up
Simple, scalable magnesium-matrix chemistry vs. complex LNP/AAV; CMC detail in this room.
IP defensibility
27+ patent portfolio incl. composition-of-matter; regional filings EU/JP/CN/AU.
Key-person dependency
Documented inventor + credentialed SAB across Mahidol, UC Davis, Karolinska, DRDC.
09 — Document vault
Primary documents behind every claim — released to qualified partners under NDA. (Attach the real files here before sharing.)
Peer-reviewed papers (PDF pack)
10 hero papers
Granted patent documents
6 flagship + portfolio
FDA orphan designation letters
V5 #457714 · V7 filing
BIOTEC / NSTDA lab reports
ASFV · shrimp
Clinical trial protocols
V5 / V7
Corporate & cap-table docs
incorporation · IP assignments
Request the full technical & financial package — CMC, regulatory plan, projections and licensing terms — and a call with the scientific and commercial team.