CME/CE
Jointly provided by Partners for Advancing Clinical Education (PACE) and DKBmed, LLC.
Acknowledgement
This activity is supported by an independent educational grant from Bristol Myers Squibb.
Target Audience
This activity is intended for physicians, physician assistants, and nurse practitioners who care for patients with metastatic melanoma.
Educational Objectives
Upon completion of this activity, participants should be able to:
- Assess the efficacy and safety of anti-LAG-3/PD-1 combination regimens (approved and under investigation) for patients with metastatic melanoma
- Discuss the role for dual LAG-3/PD-1 checkpoint blockade regimens in treatment plans for patients with metastatic melanoma
Faculty and Disclosure of Conflicts of Interest
PACE requires instructors, planners, managers, and other individuals who are in a position to control the content of this activity to disclose all financial relationships they may have with ineligible companies. All relevant financial relationships are thoroughly vetted and mitigated according to PACE policy. PACE is committed to providing learners with high-quality accredited CE activities and related materials that promote improvements or quality in healthcare and not the specific proprietary business interest of an ineligible company.
Faculty / Presenter Reported Financial Relationship
The PACE planners and others have no relevant financial relationship(s) to disclose with ineligible companies. The DKBmed planners and others have no relevant financial relationship(s) to disclose with ineligible companies. Faculty Conflicts of Interest
Omid Hamid, MD Chief, Translational Research & Immuno-Oncology
Co-Director, Cutaneous Malignancies
The Angeles Clinic & Research Institute, a Cedars Sinai Affiliate
Professor, Department of Medicine – Cedars Sinai Medical Center
Los Angeles, CA
Contracted Research for Institution: Arcus; Aduro; Akeso; Amgen; Bioatla; BMS; CytomX; Exelixis; Roche Genentech; GSK; Immunocore; Idera; Incyte; Iovance; Merck; Moderna; Merck-Serono; NextCure; Novartis; Pfizer; Sanofi Regeneron; Seagen; Taiga; Torque; Zelluna
Speakers Bureau: BMS, Novartis, Pfizer, Sanofi Regeneron
Advisory Board: Aduro; Alkermeres; Akeso; Amgen; Beigene; Bioatla; BMS; Roche Genentech; Gigagen; GSK; Immunocore; Idera; Incyte; Janssen; Merck; NextCure; Novartis; Partner Therapeutics; Pfizer; Sanofi Regeneron; Seagen; Tempus; ZellunaFee Information
Joint Accreditation Statement
In support of improving patient care, this activity has been planned and implemented by Partners for Advancing Clinical Education (PACE), DKBmed, and the Institute for Johns Hopkins Nursing. PACE is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Physician Continuing Education
PACE designates this enduring material for a maximum of 0.5 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Nursing Continuing Professional Development
The maximum number of hours awarded for this Nursing Continuing Professional Development activity is 0.5 contact hours.
PA Continuing Medical Education
PACE has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.5 AAPA Category 1 CME credits. Approval is valid until September 14th, 2024. PAs should only claim credit commensurate with the extent of their participation.
Disclosure of Unlabeled Use
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity do not recommend the use of any agent outside of the labeled indications. The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of the planners. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
Disclaimer
Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patient’s conditions and possible contraindications and/or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
There are no fees for participating and receiving CME/CE credit for this activity.
Request for Credit
If you wish to receive acknowledgment for completing this activity, please complete the evaluation.
- Release date: September 15, 2023
- Expiration date: September 14, 2024
Estimated time to complete the activity: 30 minutes
Hardware & Software Requirements
To access activities, users will need:
- A computer with an internet connection
- An HTML5 compliant web browser or Internet Explorer 8 (and higher)
Contact Information
For additional information about the accreditation of this activity, please visit https://partnersed.com