TY - JOUR
T1 - Olanzapine/Samidorphan in Young Adults With Schizophrenia, . Schizophreniform Disorder, or Bipolar I Disorder Who Are Early in Their Illness
T2 - Results of the Randomized, Controlled ENLIGHTEN-Early Study
AU - Kahn, René S.
AU - Kane, John M.
AU - Correll, Christoph U.
AU - Arevalo, Christina
AU - Simmons, Adam
AU - Graham, Christine
AU - Yagoda, Sergey
AU - Hu, Beibei
AU - McDonnell, David
N1 - Publisher Copyright:
© 2023 Physicians Postgraduate Press, Inc.
PY - 2023/5
Y1 - 2023/5
N2 - Objective: Patients with early-phase schizophrenia or bipolar I disorder (BD-I) are at greater risk for antipsychotic-associated weight gain. This 12-week, randomized, double-blind study conducted between June 2017 and December 2021 evaluated weight effects of combination olanzapine and samidorphan (OLZ/SAM) versus olanzapine in early-phase illness. Methods: Young adults (16–39 years) with DSM-5 schizophrenia, schizophreniform disorder, or BD-I, < 4 years since symptom onset, body mass index < 30 kg/m2, and < 24 weeks’ cumulative antipsychotic exposure were randomized to OLZ/SAM (5–20/10 mg/d) or olanzapine (5–20 mg/d). Primary endpoint was percent change from baseline body weight at week 12. Secondary endpoints, tested hierarchically, were proportions of patients with ≥ 10% or ≥ 7% weight gain, waist circumference change, and Clinical Global Impressions-Severity (CGI-S) change. Results: Of 428 patients (OLZ/SAM, n = 213; olanzapine, n = 215), 408 had ≥ 1 postbaseline weight assessment and were analyzed. Percent weight change was significantly lower with OLZ/SAM versus olanzapine (4.91% vs 6.77%; least-squares mean [LSM] [SE] difference, −1.87% [0.75]; P= .012). Although fewer patients treated with OLZ/SAM had ≥ 10% weight gain, the difference was not statistically significant versus olanzapine (21.9% vs 30.4%, respectively; OR = 0.64; 95% CI = 0.39 to 1.05); hierarchical testing precluded further statistical evaluation of secondary endpoints. Proportions of patients with ≥ 7% weight gain (33.1% vs 44.8%; OR = 0.61, 95% CI = 0.39 to 0.94) and waist circumference change (2.99 vs 3.90 cm; LSM [SE] difference, −0.92 cm [0.58]; 95% CI = −2.06 to 0.22) favored OLZ/SAM. LSM (SE) CGI-S change with OLZ/SAM was −0.82 (0.06). OLZ/SAM and olanzapine had similar safety profiles, including small, similar metabolic parameter changes. Conclusions: In patients with early-phase schizophrenia, schizophreniform disorder, or BD-I, OLZ/SAM treatment resulted in less weight gain versus olanzapine.
AB - Objective: Patients with early-phase schizophrenia or bipolar I disorder (BD-I) are at greater risk for antipsychotic-associated weight gain. This 12-week, randomized, double-blind study conducted between June 2017 and December 2021 evaluated weight effects of combination olanzapine and samidorphan (OLZ/SAM) versus olanzapine in early-phase illness. Methods: Young adults (16–39 years) with DSM-5 schizophrenia, schizophreniform disorder, or BD-I, < 4 years since symptom onset, body mass index < 30 kg/m2, and < 24 weeks’ cumulative antipsychotic exposure were randomized to OLZ/SAM (5–20/10 mg/d) or olanzapine (5–20 mg/d). Primary endpoint was percent change from baseline body weight at week 12. Secondary endpoints, tested hierarchically, were proportions of patients with ≥ 10% or ≥ 7% weight gain, waist circumference change, and Clinical Global Impressions-Severity (CGI-S) change. Results: Of 428 patients (OLZ/SAM, n = 213; olanzapine, n = 215), 408 had ≥ 1 postbaseline weight assessment and were analyzed. Percent weight change was significantly lower with OLZ/SAM versus olanzapine (4.91% vs 6.77%; least-squares mean [LSM] [SE] difference, −1.87% [0.75]; P= .012). Although fewer patients treated with OLZ/SAM had ≥ 10% weight gain, the difference was not statistically significant versus olanzapine (21.9% vs 30.4%, respectively; OR = 0.64; 95% CI = 0.39 to 1.05); hierarchical testing precluded further statistical evaluation of secondary endpoints. Proportions of patients with ≥ 7% weight gain (33.1% vs 44.8%; OR = 0.61, 95% CI = 0.39 to 0.94) and waist circumference change (2.99 vs 3.90 cm; LSM [SE] difference, −0.92 cm [0.58]; 95% CI = −2.06 to 0.22) favored OLZ/SAM. LSM (SE) CGI-S change with OLZ/SAM was −0.82 (0.06). OLZ/SAM and olanzapine had similar safety profiles, including small, similar metabolic parameter changes. Conclusions: In patients with early-phase schizophrenia, schizophreniform disorder, or BD-I, OLZ/SAM treatment resulted in less weight gain versus olanzapine.
UR - http://www.scopus.com/inward/record.url?scp=85150803167&partnerID=8YFLogxK
U2 - 10.4088/JCP.22m14674
DO - 10.4088/JCP.22m14674
M3 - Article
C2 - 36946605
AN - SCOPUS:85150803167
SN - 0160-6689
VL - 84
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 3
M1 - 22m14674
ER -