Newsletter | October 14, 2024

10.14.24 -- Oral Small Molecule Targeting Of Cancer With Cantex' Stephen Marcus

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Join Drug Delivery Leader Live in discussing human factors risk analysis approaches for combination products and medical devices. Central to the conversation will be the FDA’s draft guidance on Use-Related Risk Analysis (URRA) and how this guidance is related to other risk tools, such as a use Failure Mode and Effects Analysis (uFMEA). Secure your spot for this free digital event happening November 13th.

FEATURED EDITORIAL

Oral Small Molecule Targeting of Cancer with Cantex' Stephen Marcus

Dr. Stephen Marcus boasts drug development experience across various routes of administration targeting varied therapeutic areas. Now as Cantex CEO, he leans on his background as an oncologist to drive his passion for effectively treating cancer while easing the patient experience. In this episode of Sit and Deliver, host Tom von Gunden asks Dr. Marcus about innovations in small molecule delivery for complex, life-threatening conditions.

INDUSTRY INSIGHTS

Compliance Considerations For Emergency-Use Delivery Systems

Because auto-injectors are typically the delivery device of choice for emergency medications, they come with increased scrutiny from regulatory bodies regarding their safety and effectiveness.

Imaging Large Volume Subcutaneous Injections To Inform Clinical Design

New higher volume, higher viscosity pharmaceutical formulations for subcutaneous injection, alternatives to traditional intravenous treatment, enable chronic disease therapy in alternate settings.

Switching From Vials To PFS And Intravenous To Subcutaneous Formulations

Learn about formulation development challenges for prefilled syringes as well as considerations for reducing the time it takes to launch safer, more convenient, and cost-effective products for the patient.

Advances In Oral GLP-1 Analogs For Obesity

Discover how these groundbreaking Oral GLP-1 Analogs therapies are reshaping obesity management and addressing key challenges in formulation and delivery.

Zydis Orally Disintegrating Tablet (ODT) Vs. Standard Tablets (ST)

Review how Zydis ODT compares against standard oral tablets, how the same molecule can produce a different outcome when utilizing Zydis ODT, and findings from over 20 published studies.

Using Injectable Packaging: Early Development To Commercialization

While in their early-stage development of a mAb biosimilar for oncology treatment, a large biopharm sought a packaging recommendation: a stopper to maintain high-quality standards.

SOLUTIONS

Small, Simple-To-Use Package For Delivering High-Viscosity Formulations

Dry Powder Inhaler Services

Highly Flexible And Customizable On-Body Delivery System Platform

Improve The Bioavailability Of Poorly Soluble Drugs