Long-term treatment with esketamine nasal spray in patients with treatment resistant depression: Results from the ESCAPE-LTE study
Optimising patient outcomes in treatment resistant depression (TRD) requires treatments which provide sustained remission, without relapse, and tolerability in the long term. ESCAPE-LTE (NCT04829318) was a phase IV, single-arm, 2-year (104 weeks) long-term extension of ESCAPE-TRD (NCT04338321; 32 weeks), a rater-blinded, randomised, active-controlled trial, which evaluated the safety, tolerability and efficacy of esketamine nasal spray (NS), alongside an ongoing selective serotonin reuptake inhibitor/serotonin-norepinephrine reuptake inhibitor, in patients with TRD. The primary endpoints were the proportion of patients who reported treatment-emergent adverse events (TEAEs) or suicidal ideation and behaviour (using the Columbia-Suicide Severity Rating Scale). Effectiveness was assessed using the Montgomery-Åsberg Depression Rating Scale, Clinical Global Impression-Severity scale, Patient Health Questionnaire-9 and EuroQol 5-Dimension 5-Level questionnaire. Outcomes are reported from ESCAPE-TRD baseline to the end of ESCAPE-LTE (136 weeks of treatment, 138 weeks including safety follow-up). In patients who entered ESCAPE-LTE (N = 183), TEAEs and serious TEAEs were observed in 96.7% and 8.2%, respectively. 98.3% of TEAEs occurring on dosing days resolved same-day; few patients discontinued due to TEAEs during ESCAPE-LTE (3.3%). 151/160 (94.4%) patients who were non-suicidal at baseline remained non-suicidal to the end of ESCAPE-LTE. In the subgroup with remission in ESCAPE-TRD, 79.2% did not relapse or discontinue treatment throughout ESCAPE-LTE; the overall relapse rate for patients achieving remission across both studies was 6.9%. The vast majority of patients with TRD who achieved remission with esketamine NS did not relapse over 136 weeks of treatment; no new safety concerns were identified, and the safety profile was consistent with short-term studies.
Authors
- A. Oliveira-Maia
- RE Nielsen
- W.J. Cubała
- J Buyze
- Yağcıoğlu AE Anıl
- A Reif
- L Haggström
- R Frey
- Young AH
- Fu DJ
- C von Holt
- Y Godinov
- Y Kambarov
- I Bitter
Institutions
- Semmelweis University (HU)
- Champalimaud Foundation (PT)
- Johnson & Johnson (United States) (US)
- Aalborg University Hospital (DK)
- Fraunhofer Institute for Translational Medicine and Pharmacology (DE)
- Johnson & Johnson (Germany) (DE)
- Imperial College London (GB)
- Hacettepe University (TR)
- Gdańsk Medical University (PL)
- Medical University of Vienna (AT)
- Universidade Nova de Lisboa (PT)
- Aalborg University (DK)
Publication Details
- Journal
- European Neuropsychopharmacology
- Published
- 2026-02-27
- DOI
- https://doi.org/10.1016/j.euroneuro.2026.112801
- Citations
- 1
- Primary Topic
- Treatment of Major Depression
- Type
- article
- Field-Weighted Citation Impact
- 32.57