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Article History

Received: 16 February 2020

Accepted: 14 July 2020

First Online: 31 July 2020

Ethics approval and consent to participate

: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Tulane University Human Research Protection Office IRB (IRB #2018–879) reviewed the study materials, approved the method of consent and provided approval for the study. Enrolled patients provided informed consent to participate via electronic signature.

: Not applicable.

: EB Geer is an employee of Memorial Sloan Kettering which received research support from Chiasma, Inc.; J Sisco and D Adelman have served as consultants and are members of Advisory Boards for pharmaceutical companies other than Chiasma, Inc.; WH Ludlam, A Haviv are employees of Chiasma, Inc.; D Gelbaum was an employee of Chiasma, Inc. at the time of the research; S Lui and L Shi are employees of Tulane University, which received funding from Chiasma, Inc. for conducting this study.; SD Mathias is an employee of Health Outcomes Solutions, which received funding from Chiasma, Inc. for assisting in the conduct of this study.