An Open Label Study of NLS-2 (Mazindol Extended Release) in Subjects With Narcolepsy

Inclusion Criteria

• •The subject must complete all Study NLS-1021 study requirements and assessments up to Visit 6;
• •The subject is able, in the opinion of the Investigator, to receive NLS-2 for the 24-week Treatment Phase of this study;
• •Biological females of childbearing potential must agree to use a medically acceptable double-barrier method of contraception for at least 30 days prior to Day 1 and until completion of the study;
• •The subject is able to comply with the open-labelled extension design schedule and other study requirements;
• •The subject provides written informed consent for the open-label extension study.