PODD 2026 · SHERATON BOSTON HOTEL · OCTOBER 29–30, 2026

MEET ARx AT PODD BOOTH 1304

Do you have a compound whose bioavailability has stalled its path to first-in-human, or an approved asset where poor adherence is undercutting an effect the science already proved? Either way, the molecule isn’t the problem. The delivery route is.

ARx has spent over two decades closing that gap, building oral thin film and transdermal formats that get more of a compound into circulation and give underserved patients a reliable way to take it.

As a fourth-generation, family-owned drug delivery partner and CDMO, we pair your molecule with our proven delivery formats to offer a faster path to clinic.

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years in drug delivery

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Years Commercial Manufacturing
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Positive FDA Inspections
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GETTING STARTED WITH ARx

Wherever Your Program Stands, There's a Path Forward

Whether a program is starting from a blank formulation, an approved asset needing a new format, or a stalled transfer with nowhere to go, ARx can take it on.

New Development

The same team that runs feasibility screening carries a program through NDA or ANDA filing and into commercial-scale production, with no handoff and no one re-learning the compound partway through.

Reformulation & IP Differentiation

An approved asset isn’t locked into its original format. When a patent window is closing or a formulation is losing patients to poor adherence, a new delivery route can be the fix, and ARx carries that reformulation through to commercial launch.

Tech Transfer Capabilities

When a program needs a new manufacturing home, process knowledge has to move with it. ARx has handled complex transfers across oral thin film and transdermal formats, including programs other CDMOs could not deliver on.

Delivery Built for the Patient

Oral thin film and transdermal formats improve therapeutic onset and strengthen patient adherence. For programs indicated for elderly, pediatric, or oncology populations, that distinction is clinical, not cosmetic.

FOR COMPOUNDS THAT NEED FLEXIBLE ABSORPTION ROUTES

Oral Thin Film Delivery Platforms

LINGUAL THIN FILMS

Sits on the tongue and dissolves within 5 to 30 seconds, releasing API into saliva for absorption through the GI tract. It supports drug loading up to 65mg across salts, free-base compounds, and potent APIs, making it a practical option for patients with dysphagia, including pediatric and geriatric populations.

SUBLINGUAL THIN FILMS

Placed under the tongue, it dissolves and enters systemic circulation directly through the sublingual mucosa, bypassing hepatic first-pass metabolism entirely. In human studies, API appeared in plasma within 5 minutes, with peak concentration reached by 30 minutes, the fastest onset of any oral route.

BUCCAL THIN FILMS

Adheres to the inner cheek, releasing API through the buccal mucosa over a controlled window of 30 minutes to 12 hours while also bypassing first-pass metabolism. In testing, buccal films achieved 2x the systemic exposure of conventional formats at just 25% of the drug loading, with no toxic metabolites detected.

FOR COMPOUNDS THAT NEED SYSTEMIC OR LOCALIZED DELIVERY

Transdermal Patch Delivery Platforms

TRANSDERMAL PATCHES

Applied to the skin, it routes API directly into systemic circulation, bypassing GI transit and first-pass hepatic metabolism entirely. Controlled release extends up to 7 days per application, supported by enhancer combinations engineered to keep plasma levels steady over time.

TOPICAL PATCHES

Positioned at the treatment site itself, it confines exposure to local tissue rather than systemic circulation. Release rate and duration are calibrated to the indication, tissue type, and API permeability, limiting the risk of side effects that come with broader systemic exposure.

FOR POTENT, LOW-DOSE COMPOUNDS

MicroDEP Ultra-Low-Dose Oral Thin Film

ARx’s proprietary micro-deposition technology deposits micro-sized formulations directly onto the film surface, rather than dispersing them through a polymer matrix, giving high-potency and hard-to-formulate compounds a level of dosing precision conventional film loading can’t reach.

Which Programs Commonly Qualify?

4x

API concentration at 30 minutes vs. conventional films

5 minutes

to detectable plasma levels post-dose

10 μg

of dose precision, from Phase I through commercial scale

2

Thin film formats available: buccal and sublingual

MEET ARx AT BOOTH 508

Whether a delivery question is still open on one of your programs, or you’re evaluating a partner with real commercial-scale depth across oral thin film and transdermal delivery, we’d like to talk it through at PODD