A 3-Month Open-Label Safety and Efficacy Study of TNX-102 SL Tablets in Fibromyalgia Patients

The study consist of 4 study visits, including Screening/Baseline Visit 1 (Day 0, which is
anticipated to be the same date as Visit 6 in F301 or F302) and visits after 1, 2 and 3
months of treatment (Visits 2-4).

Primary:

The primary objective of the study is to evaluate the safety of TNX-102 SL tablets taken
daily at bedtime over an additional 3 months in patients with FM who have completed the
double-blinded lead-in study

Secondary:

The secondary objective is to evaluate the efficacy of TNX-102 SL tablets taken daily at
bedtime to control symptoms of FM

Inclusion Criteria:

- The patient met all prior inclusion and exclusion requirements for study F301 or F302
originally, and has had no intervening medical conditions, increased suicidal
ideation, or requirements for concomitant medications that preclude exposure to
TNX-102 SL or enrollment in the extension study.

- The patient completed expected dosing in F301 or F302 defined as taking study
medication up to Week 12, with at least 70% compliance with medication usage (based on
overall drug accountability reconciliation at the end of the F301 or F302 lead-in
study) and no major protocol deviations.

- The patient has provided written informed consent to participate in this extension
protocol.

Exclusion Criteria: