A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 03

Exclusion Criteria

• •Able to provide written informed consent (IC) prior to any study procedures and willing and able to comply with study procedures
• •In the opinion of the investigator, the participant demonstrated adequate compliance with the study procedures in Study RLM-MD-01 or RLM-MD-02
• •Participants are excluded from the study if any of the following criteria apply:
• •Participant is not willing or able to abide by the restrictions regarding concomitant medicine use
• •Participant is planning to receive an investigational drug (other than study treatment) or investigational device at any time during Study RLM-MD-03
• •Participant has an unresolved adverse event (AE) or a clinically significant finding on physical examination, clinical laboratory test, or 12-lead electrocardiogram (ECG) that, in the investigator's opinion, would limit the participant's ability to participate in or complete the study
• •Any other reason that, in the investigator's opinion, would confound proper interpretation of the study or expose a participant to unacceptable risk, including renal, hepatic or cardiopulmonary disease