Discussing Clinical and Payer Insights to Encourage the Adoption of Oncology Biosimilars into Practice
On-Demand Free Accredited Multidisciplinary Panel Discussion
This activity is supported by independent medical education grants from
Sandoz Inc., a Novartis Division, and Coherus BioSciences.
Sandoz Inc., a Novartis Division, and Coherus BioSciences.
Faculty Panel
Leigh M. Boehmer, PharmD, BCOP
Medical Director
Association of Community Cancer Centers
Rockville, Maryland
Rebecca Borgert, PharmD, BCOP
Senior Director, Oncology Clinical Strategy and Innovation
Magellan Rx Management
Orlando, Florida
Sanjiv S. Agarwala, MD
Professor, Temple University School of Medicine
Philadelphia, Pennsylvania
Chief Medical Officer
Cancer Expert Now, Inc.
Morristown, New Jersey
Medical Writing Support
Lori Huang, BS, PharmD, BCPS
Medical Writer, Clinical Pharmacist
Ann Arbor, Michigan
Program Description
The number of available biosimilars on the market for oncology-related indications continues to increase. The manufacturing and development process of biosimilars can be complex, and clinicians may be reluctant to modify prescribing practices or formularies because of these factors. Uncertainty about risks and benefits of oncology biosimilars and their use for either supportive care or treatment has been documented as a barrier to biosimilar uptake. Managed care professionals and pharmacists working with biosimilars need to maintain consistent messaging to both clinicians and patients about their use. The multidisciplinary discussion will cover topics such as extrapolation, interchangeability, and implementation challenges for preferred formulary agents that managed care professionals will encounter when incorporating biosimilars into clinical practice. The panelists will also present strategies and practice guidelines that can be employed to help guide the adoption and optimization of use of oncology biosimilars.
Target Audience: Managed care and oncology pharmacists
Type of Activity: Application
Release date: August 6, 2021
Expiration date: August 6, 2022
Fee: Free
Educational Objectives
At the completion of this activity, participants will be able to:
- Classify the core concepts that drive the biosimilar approval process and identify how it differs from the approval of an originator biologic.
- Examine the available and emerging oncology biosimilars, their indications, and their originator biologics.
- Identify clinical and nonclinical barriers that affect the implementation of oncology biosimilars in clinical practice.
- Differentiate the roles of pharmacists, oncologists, and payers in developing strategies to implement oncology biosimilars in clinical practice.
Pharmacy Times Continuing Education™ is accredited by the Accreditation Council for Pharmacy Education (ACPE) as a provider of continuing pharmacy education. This activity is approved for 1.5 contact hours (0.15 CEU) under the ACPE universal activity number 0290-0000-21-296-H01-P. The activity is available for CE credit through August 6, 2022. This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of Physicians’ Education Resource®, LLC, and Pharmacy Times Continuing Education™. Physicians’ Education Resource®, LLC is accredited by the ACCME to provide continuing medical education for physicians.
Physicians’ Education Resource®, LLC designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Physicians’ Education Resource®, LLC is approved by the California Board of Registered Nursing, Provider #16669, for 1.5 Contact Hours.
Instructions for Completing the Activity and Receiving CPE Credit
To receive CPE credit, participants must complete the pretest, view the webcast in its entirety, complete the posttest, and complete the online activity evaluation. After successful completion of the online activity evaluation, you can submit your credit to CPE Monitor. You may view your credit within 48 hours at www.mycpemonitor.net. All participants must request credit before the activity expiration date. CE credit will not be issued after this date.
Disclosures
Faculty
Leigh M. Boehmer, PharmD, BCOP, has the following relevant financial relationship with a commercial interest to disclose:
- Consultant: Pfizer
Rebecca Borgert, PharmD, BCOP, has the following relevant financial relationships with commercial interests to disclose:
- Consultant: Seagen
- Spouse: Spouse is an employee of Melinta Therapeutics
Faculty
Sanjiv S. Agarwala, MD
Medical Writing Support
Lori Huang, BS, PharmD, BCPS
Pharmacy Times Continuing Education™ Planning Staff – Jim Palatine, RPh, MBA; Maryjo Dixon, RPh; Amy H. Seung, PharmD, BCOP, FHOPA; Kelly McCormick; Susan Pordon; Brianna Winters; and Chloe Taccetta have no relevant financial relationships with commercial interests to disclose.
Anonymous peer reviewers are used as part of content validation and conflict resolution. The peer reviewers have no relevant financial relationships with commercial interests to disclose.
Activity Disclaimer
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Educational Disclaimer
CPE activities are offered solely for educational purposes and do not constitute any form of professional advice or referral. Discussions concerning drugs, dosages, and procedures may reflect the clinical experience of the author(s) or they may be derived from the professional literature or other sources and may suggest uses that are investigational in nature and not approved labeling or indications. Participants are encouraged to refer to primary references or full prescribing information resources.
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