Enhancing Bioavailability and Manufacturability for Oral Small Molecule

Enhancing Bioavailability and Manufacturability for Oral Small Molecule

By Pharmaceutical & BioScience Society

Overview

Enhancing Bioavailability and Manufacturability with Enabling Formulation Technologies for Oral Small Molecule Drug Product Development

Registration: for regular attendees, register at our webiste https://www.pbss.org/eventDetails/1006
Regular attendees: $295; Academic or Self Paying: $45 ($45 registration closes on 11/25/2025); Major Sponsorship: $3000; Vendor Show: $750, Happy Hour Sponsorship: $1,250; Lunch Sponsorship: $1,500; On-site Registration: $500. Please note: Registration may close earlier than the posted deadline once the set number of participants has been reached.

Event Description:

It is well known that a majority of small molecule late discovery and development pipelines are populated by compounds that are poorly soluble, and/or permeable. This has resulted in increasing use of established and emerging technologies to address these limitations. There are multiple ways that enabling technologies are impactful on the overall drug development effort, among them:

  • Rendering poorly soluble molecules into tractable entities, with respect to: Solubility, Supersaturation on dissolution, Absorption and PK profile
  • Enhancing the ability to efficiently modify and optimize the performance of drug products in response to pre-preclinical, preclinical and early clinical in vivo data
  • Helping to ensure that the dosage form(s) used in clinical development are appropriate to the target, with respect to pharmacokinetic (PK) and pharmacodynamic (PD) profiles

The workshop will describe and discuss approaches, with case studies, that address the iterative, interdependent, multidisciplinary nature of effective drug product development, with focus on small molecules that require enabling technologies.

Topics:

  • Use of Quality Target Product Profiles (QTPPs) to guide product development strategy (single presentation)
  • The state of the art in enabling technologies (SDDs, HME/kinetisol, Lipid-based, nanoparticles, other)
  • Translational aspects of formulation development and drug product development
  • Use of AI/ML and lab automation to optimize and test attributes and feasibility of pharmaceutical blends
  • 3D printing for drug product manufacture

Lineup

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Highlights

  • 8 hours 45 minutes
  • In person

Refund Policy

Refunds up to 7 days before event

Location

Hilton San Francisco Airport Bayfront

600 Airport Boulevard

Burlingame, CA 94010

How do you want to get there?

Agenda
8:00 AM - 9:00 AM

PBSS Overview

Shichang Miao, PhD, PBSS
9:00 AM - 9:15 AM

Welcome and Workshop introduction

Stuart Levy, PhD, SGL Chemistry Consultin
9:15 AM - 10:00 AM

IP Considerations for Development and Implementation of Enabling Technologies

Presented by Julia Minitti, PhD, JD, Partner, Wilson Sonsini Goodrich & Rosati

Organized by

Pharmaceutical & BioScience Society

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$423.34
Dec 2 · 8:45 AM PST