CAPRO™ Platform
Patented polymer excipient · Release by design
MORE™ Platform
Patent-pending oral wafer · OTC + Rx
Long-Acting Injectables
SubQ · IM · IA · Biodegradable implant

MORE™ —
The oral format people
actually choose.

MORE™ is Trekka's patent-pending multi-layer oral wafer. Dissolves on the tongue, buccal mucosa, or sublingually — no water required. A highly tunable layer architecture — active APIs, taste masking, extended release, tunable mucoadhesion, and optional CAPRO™-enhanced solubilization when the API calls for it. One platform. OTC to market fast. Rx value long-term.

Patent pending Tunable dissolution · release kinetics · mucoadhesion No water required Sublingual · Buccal · On-tongue delivery
MORE™ Wafer — Highly tunable layer architecture
Active ingredient layer
Fast onset
Required
Taste-masking / comfort
If needed
Optional
Second active ingredient
Extended / biphasic
If needed
CAPRO™-enhanced solubilization
When API requires it
Optional
Dissolution modifier / base
As required
Optional
Each wafer is formulated for the specific API and application. Layer count, composition, and sequence are determined by the clinical need — not a fixed template. CAPRO™ is incorporated only when the API delivery profile requires it.
Active drug layer
Optional functional layer
CAPRO™-enhanced (optional)
Tunable
Layer architecture
Designed per application
0
Water needed
Dissolves on the tongue
3
Delivery routes
SL · Buccal · On-tongue
The problem

Nobody likes swallowing pills — and many simply can't.

The elderly struggle with swallowing. Children resist tablets. Patients with dysphagia, dry mouth, or post-surgical conditions cannot take conventional pills reliably. Poor adherence follows — and outcomes fall short of what the drug can actually do.

Delivery criterion Conventional pill / tablet MORE™ oral wafer
Water requirementAdministration barrier Requires water and swallowing — excludes elderly, pediatric, dysphagia patients and many care settings Dissolves on the tongue in seconds — no water, no swallowing, no administration barrier
Adherence rateReal-world compliance Up to 50% of patients skip or miss daily oral medications — the format itself drives non-adherence Convenient, discreet, water-free — removes the primary compliance barrier for daily oral therapy
Absorption routeOnset and PK variability GI absorption — slow, variable, subject to food effects and first-pass hepatic metabolism Transmucosal absorption — bypasses GI and first-pass, faster onset, more consistent systemic exposure
Release profilePK programmability Single release profile — fast-dissolve OR extended, not both. One API per conventional tablet practical limit. Tunable multi-layer architecture — fast, extended, or biphasic from a single wafer, with multiple APIs independently controlled
Poorly soluble APIsBCS II / IV formulation Standard oral excipients offer limited solubility enhancement — BCS IV molecules often not viable as tablets Optional CAPRO™-enhanced layers available when the API requires solubilization support — not a requirement for every formulation
Market reachOTC and Rx addressability Tablets can serve either OTC or Rx — the same platform rarely spans both markets with meaningful differentiation Identical platform — OTC generates near-term revenue, Rx builds clinical IP. Both from one technology investment.
How it works

Four steps — from placement to therapeutic effect.

The entire delivery sequence is designed to eliminate every friction point a conventional oral dose form creates.

1
Oral placement
Placed sublingually, buccally, or on the tongue. No water. Mucoadhesive properties hold it in place.
wafer
2
Tunable dissolution
Each layer dissolves on its own programmed timeline — fast, extended, or biphasic — determined by the formulation need, not the format.
3
Transmucosal absorption
API crosses the sublingual mucosa directly into systemic circulation — bypassing GI and first-pass metabolism. Faster onset, cleaner PK.
Faster onset · Better PK
4
Controlled multi-layer release
Additional layers deliver extended or biphasic release on their own programmed timescales — with optional CAPRO™ enhancement when solubilization is needed.
Biphasic profile — one wafer
Transmucosal vs oral tablet — the key difference
Sublingual absorption bypasses GI transit and first-pass hepatic metabolism. For CNS, pain, and acute-care indications where speed of onset matters clinically, this is a therapeutic advantage — not a convenience feature.
Platform capabilities

What makes MORE™ different — by design.

Every capability is a direct answer to a documented limitation of tablets, capsules, and oral liquids.

No water · Transmucosal delivery
Dissolves on the tongue in seconds — no swallowing, no water, no administration barrier. Bypasses GI degradation and first-pass metabolism for faster onset, more consistent absorption, and access to populations tablets exclude.
Broadest reach · Better PK
Tunable dissolution, release kinetics, mouthfeel & texture
Fast, extended, or biphasic dissolution profiles engineered into the layer architecture before manufacture. Mouthfeel, texture, and taste are independently tunable parameters — not afterthoughts. Release kinetics are pre-programmed by design, not approximated in vivo by excipient ratios.
Precision PK + patient experience
Multi-layer architecture
Independently engineered layers — active APIs, taste masking, dissolution control, optional CAPRO™ solubilization — enabling multi-API delivery no tablet can replicate.
Multi-API capable
505(b)(2) regulatory path
Reformulating an approved API into a MORE™ wafer keeps the active ingredient unchanged — the full established safety database travels with the program. 505(b)(2) is the default Rx path, designed in from day one. OTC applications require no IND at all.
Faster to NDA
Biologic compatibility
Solvent-free, room-temperature processing preserves protein and peptide structural integrity. CAPRO™ enhancement can be incorporated into the layer architecture when the API requires additional stabilization.
Labile API capable
Tunable mucoadhesion
When the application requires extended mucosal contact time — for improved absorption, sustained local delivery, or site-specific targeting — mucoadhesion can be engineered into the wafer layer architecture as an independent tunable parameter.
Extended mucosal contact
50%
Patient non-adherence
Of daily oral medication users skip or miss doses — primarily because the format is inconvenient
Wafer removes this barrier
Delivery routes
Sublingual, buccal, and on-tongue — all three transmucosal routes supported from one wafer format, tuned per application
Format flexibility
505(b)(2)
Regulatory path
Reformulating an approved API into MORE™ leverages existing safety data — faster IND to NDA, lower capital requirement
Rx-ready by design
Platform synergy

MORE™ standalone — or enhanced with CAPRO™.

MORE™ is a complete oral delivery platform on its own. For APIs that require solubilization support — BCS Class II/IV molecules, poorly soluble drugs — CAPRO™-enhanced layers can be incorporated. The combination delivers tunability no competing platform can match.

CAPRO™ + MORE™ combined capability
CAPRO™
Optional enhancement
When API needs it
+
MORE™
Oral delivery platform
Wafer architecture
Result
Drug delivery tunability no competing platform can deliver
What becomes possible with CAPRO™-enhanced MORE™ wafers:
BCS IV molecules — formulated into a sublingual wafer for the first time
Multi-drug combination wafers — fast-onset relief + extended anti-inflammatory in one
Poorly soluble consumer APIs — OTC wafer format with CAPRO™ solubilization built in
Lifecycle extension — tablet drug converted to patented, clinically differentiated wafer
What each platform contributes
MORE™ Oral delivery platform — standalone or combined
Sublingual, buccal, and on-tongue delivery — all three routes
Tunable multi-layer architecture — designed for each application
No water required — removes #1 compliance barrier
OTC and Rx markets — dual revenue from one platform
CAPRO™ Optional enhancement — incorporated when the API requires it
Solubilizes BCS II/IV poorly soluble molecules in wafer layers
Stabilizes biologics — room temperature, solvent-free
Pre-programs release kinetics via cleavable linkers
Not required — used only when the formulation calls for it
No other platform combination achieves this. Competing technologies may offer sublingual delivery or enhanced solubility — not both, in a single patent-pending wafer, across OTC and Rx.
Applications

Where MORE™ creates the most clinical and commercial impact.

MORE™ is best suited where delivery speed, patient convenience, and format differentiation are clinically or commercially meaningful.

Fast onset CAPRO™ + MORE™
Pain
OTC wafer + Rx transmucosal
Sublingual CNS Fast mucosal uptake
CNS
Sublingual Rx · Monthly wafer
Consumer wafer OTC · fast to market
Consumer Health
Sleep · Energy · Oral health OTC
Oncology support Anti-emetic · Analgesic
Oncology Supportive
Anti-emetic · Pain wafer
Pediatric friendly No swallowing needed
Pediatrics / Geriatrics
Swallow-free oral Rx
Regulatory strategy

505(b)(2) built in from day one — not retrofitted at the end of development.

Reformulating an approved API into a MORE™ wafer qualifies for 505(b)(2) because the active ingredient is unchanged. Every Rx MORE™ program is designed around this from first molecule evaluation.

Traditional NDA — 505(b)(1)
Novel drug development path
Full preclinical safety package constructed from scratch — years of toxicology studies
All three phases of clinical trials required — Phase I, II, and III independently powered
Novel safety database built entirely independently — no existing data to reference
Capital requirement typically $100M+ to reach IND filing stage
10–15 year typical development timeline from IND to approval
MORE™ Rx path — 505(b)(2)
Reformulation of approved API
Existing published safety data for the approved API fully leveraged — no duplication
Streamlined clinical program focused on delivery differentiation — not full Phase I–III
Approved molecule as starting point — established safety profile referenced in the NDA
Significantly lower capital requirement to IND — faster commercial return on investment
Faster IND-to-approval arc — de-risked regulatory path by design, not by accident
505(b)(2) is the default — for every MORE™ Rx program, from day one
Trekka doesn't choose a regulatory pathway at the end of development. The 505(b)(2) path shapes molecule selection, formulation strategy, and clinical design from the first evaluation. OTC MORE™ products require no IND — the fastest route to commercial validation and early revenue.
Have a molecule or product idea
that should be a wafer?
Whether it's an OTC consumer product ready for a better format, a CNS or pain drug that needs faster absorption, or a poorly soluble API that no conventional oral platform can handle — tell us what you're working on.
OTC or Rx — both paths supported
CAPRO™ enhancement available for poorly soluble APIs
Response within 48 hours · Confidential