Study on Seltorexant for Adults and Elderly with Major Depressive Disorder and Insomnia Symptoms

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What is this study about?

This clinical trial is focused on studying the effects of a medication called seltorexant on adults and elderly patients who have Major Depressive Disorder with symptoms of insomnia. Major Depressive Disorder, often referred to as depression, is a condition characterized by persistent feelings of sadness and loss of interest, which can significantly impact daily life. Insomnia is a common symptom of depression, where individuals have trouble falling or staying asleep.

The purpose of the study is to evaluate how well seltorexant works when used alongside other antidepressants, specifically those known as SSRIs (Selective Serotonin Reuptake Inhibitors) or SNRIs (Serotonin-Norepinephrine Reuptake Inhibitors). The study will compare the effects of taking seltorexant with a placebo, which looks like the medication but does not contain the active ingredient. The study aims to see if seltorexant can improve depressive symptoms and help maintain these improvements over time.

Participants in the study will take part in two main parts. In the first part, the effectiveness of seltorexant in improving symptoms of depression will be assessed. In the second part, the focus will be on whether seltorexant can help prevent the return of depressive symptoms after initial improvement. The study will involve taking the medication in the form of a film-coated tablet by mouth. The trial is designed to ensure the safety and effectiveness of seltorexant as an additional treatment for those who have not fully responded to their current antidepressant therapy.

1 initial assessment

An initial assessment is conducted to confirm eligibility. This includes a physical examination, checking vital signs, and performing an ECG (a test that measures the electrical activity of the heart).

Eligibility is based on criteria such as age (18 to 74 years), a diagnosis of major depressive disorder with insomnia symptoms, and an inadequate response to certain antidepressants.

2 part 1: treatment phase

Participants receive either seltorexant 20 mg or a placebo as an additional treatment to their current antidepressant. The medication is taken orally in the form of a film-coated tablet.

The goal is to assess the effectiveness of seltorexant in improving depressive symptoms over a period of 43 days.

3 evaluation of response

The change in depressive symptoms is measured using the MADRS (Montgomery-Åsberg Depression Rating Scale) from the start of the treatment to Day 43.

Participants who show a stable response to the treatment may proceed to the next phase.

4 part 2: maintenance phase

Participants who have a stable response enter a double-blind maintenance phase. This phase aims to evaluate the ability of seltorexant to delay the relapse of depressive symptoms.

The time from randomization to the first relapse is monitored during this phase.

5 completion of trial

The trial is estimated to conclude by December 30, 2026.

Participants’ progress and any changes in symptoms are continuously monitored throughout the trial duration.

Who Can Join the Study?

  • Participants must be between 18 and 74 years old.
  • Participants should be in good health based on a physical exam, vital signs check, and heart test (12-lead ECG) done at the start of the study.
  • Participants must meet the DSM-5 criteria for Major Depressive Disorder (MDD) without any psychotic features. DSM-5 is a guide used by doctors to diagnose mental health conditions.
  • Participants should have tried at least one but not more than two antidepressants during their current depression episode, but these did not work well enough. The antidepressant should have been taken for at least 6 weeks at a stable dose.
  • Participants must be taking and handling well one of the following antidepressants: citalopram, duloxetine, escitalopram, fluvoxamine, fluoxetine, milnacipran, levomilnacipran, paroxetine, sertraline, venlafaxine, desvenlafaxine, vilazodone, or vortioxetine. The dose should be stable and at a therapeutic level for at least 6 weeks.
  • Participants should be experiencing a major depressive episode that is at least moderately severe, as measured by a specific depression scale (SIGH-D) during the screening. There should not be a significant improvement in symptoms from the start to the end of the screening.
  • Participants should have a Body Mass Index (BMI) between 18 and 40 kg/m². BMI is a measure of body fat based on height and weight.
  • Participants who are continuing from Part 1 of the study must have completed the treatment phase of Part 1.
  • Participants must be able to consistently tolerate the study medication.

Who Cannot Join the Study?

  • Participants who have a medical condition other than Major Depressive Disorder with Insomnia Symptoms.
  • Participants who have not had an inadequate response to their current SSRI/SNRI antidepressant therapy. SSRI and SNRI are types of medications used to treat depression.
  • Participants who are not within the specified age range for the study.
  • Participants who are not able to follow the study procedures or take the study medication as required.
  • Participants who are part of a vulnerable population that the study is not designed to include.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Clintrial s.r.o. Prague Czechia
A-Shine s.r.o. Plzen Czechia
Hospital Universitario General De Villalba Madrid Spain
Unidade Local De Saude De Loures-Odivelas EPE Loures Portugal
Medical Center Zara-Med EOOD Stara Zagora Bulgaria
Axstaai Oylyacghusg dk Piqumr Padua Italy
Ubxthgrxbmv nqylyqdfw Lf Ptagamib Kriddu Kosice Slovakia
Hlfhrnqz Vtrh dwepurre Barcelona Spain
Hstqznvm Chaoqk De Btlqrhmqq Barcelona Spain
Ikxpm Ourrhush Punfxfcqnce Skh Mjknjwf Genoa Italy
Urvrfrqcpi Dfskg Svmai Dg Bhuhcws Brescia Italy
Flnirgzec Pytx Ls Ivivsmnqyvldf Bexcdoife Dyz Hlpsmkat Umlhhoncrfuzx Lq Pdk Madrid Spain
Cuvd Cinhoj Cgskiqh Ahkjutvcc Bqcgh Agnnbujnrq Braga Portugal
Fsdzvemjdf Ibcfl Smu Gmwtbwy Dzl Tosflnw Monza Italy
Hfnqgqts Cko Prgmf Sgnh Porto Portugal
Auxjvch Ojrlcsqknhc Uxsostkbztsmv Pyhnev Pisa Italy
Ucdfrihlxd Mlwajdmpvrtu Hvxqecvi Fyz Azvbwm Tfhqkktry Stbpo Gkceca Ecx Plovdiv Bulgaria
Cnrrez Ftb Mcycyc Hjebke Pimtf Dqm Icgt Tetkdc Bgzwdl Emne Burgas Bulgaria
Pjbbaff sukitg Prague Czechia
Hcwkyh Pkaze Sovl Barcelona Spain
Ajlrpsr Ojcfkyixdjovdhkpwbyignecz Pwprhxefuhj Ga Rrasqmbfjjva Mnoli Db Cdxgaut Catania Italy
Sjunskbh Cayvux Jyjassih De Upgjmde Bzlkb Oradea Romania
Nvsosrvyiglrwqgt Phznchm sdbesd Prague Czechia
Sutrwdow Coplkl Do Pcdszmxuhi Sh Nzleqxdqdv Bikbxe Brasov Romania
Masqlci Cuhbfx Sfbab Ncse Eykj Sofia Bulgaria
Cyeomw fxq Mvuryy Hkyoaf “tenkb Na Sxioqecaxkphm Eehh Sofia Bulgaria
Ctclodw Zkqsuwf Rkmtbu sfwukq Bardejov Slovakia
Mszayt snxsvu Stare Mesto Slovakia
Pgeibhscqv sxntzt Rimavska Sobota Slovakia
Suebbhmmepn Wpyvomjdxa Zojipc Pmjbyzuqtph Zfluosvs Pzlwjwzzxgeclof Ohunum Ztwhujwhju W Wsinvutbr Warsaw Poland
Mnmqux soliol Brno Czechia
Oxnugko Bfmke Kyurjshwyut Cxcgxmull Sqbn Exb Glbrunxgnpsvl Musslqisct Tmdcrcu Bydgoszcz Poland
Nxsixfykurad Zssznm Opekgc Pdiqmrdighjbxig Mzfxtw Leszno Poland
Ipmoxiuynj Pczxwn dz Cytwkavwu Mdnihkhouzq prnzle Bhxa Aurqpgqdtq Eolvvxxpj si Rtbe Craiova Romania
Fzrqxkk spvuxs Prague Czechia
Dhprgunudw Azy Cnsgtnqjtoum Cowimx Sbxsuaos Ajk Swdzar Kjlif Afn Dwotau Ojs Sofia Bulgaria
Axqjrue Ojksipugpaf Uatcmkjoohajr Sqkhbm Siena Italy
Cqjwnxjpaovm Cosjriav Csizbp Lisbon Portugal
Clg Cwfvqosp Toryc Ceyqjgshgyd As Uppsala Sweden
Ahqnker Sulbdgqti Loffpk 2 Lvbfkalh Vreml Czffuq Chieti Italy
Agzgyle Opfefifhfnxuyohoosyoqnhfn Smsm Aiwbu Rome Italy
Mbd Cnnikaiz Rknnddya Pvyehph Bh Pdwsvj Warsaw Poland
Hggthtdn Ufsuiegvaljbu Ihizqqb Ljmbkk Madrid Spain
Hpwsemjq Uzofymlyqgica Bddkmug Bilbao Spain
Djgguxgylibfrzuyugrtklj Claatd Mryoece M Vpbom Ong Varna Bulgaria
Chvmtqv Mphpoywq Irfietgr Sif z oyrr Bydgoszcz Poland
Pllvpoz i Lurg At Lund Sweden
Pzcenncp Smm z ogem Bydgoszcz Poland
Chaljsu Coohwru stillt Vranov Nad Toplou Slovakia
Pzfzifd i Skylilyvu As Stockholm Sweden
Lbphuzfte Nwbkxfshj S Pzdaykbgfstg Mcmyi Iixng Slhrwmq Lfswdqedt Mvgyduk Liptovsky Mikulas Slovakia
Pqaowcwuoow Ggosrumay Soj z ozkg Grudziadz Poland
Alxunjz Skbeccyov Lxxwcw Db Syxhzov Battipaglia Italy

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Bulgaria Bulgaria
Recruiting
25.03.2025
Czechia Czechia
Recruiting
25.03.2025
Italy Italy
Not recruiting
25.03.2025
Poland Poland
Recruiting
25.03.2025
Portugal Portugal
Not recruiting
25.03.2025
Romania Romania
Not recruiting
25.03.2025
Slovakia Slovakia
Recruiting
25.03.2025
Spain Spain
Recruiting
25.03.2025
Sweden Sweden
Recruiting
25.03.2025

Trial locations

Investigated Drugs:

Seltorexant is a medication being studied for its potential to help people with major depressive disorder who also have trouble sleeping. It is used in combination with other antidepressants, specifically SSRIs or SNRIs, to see if it can improve symptoms of depression in those who haven’t responded well to their current treatment. The study is also looking at whether Seltorexant can help prevent the return of depressive symptoms after initial improvement.

Major Depressive Disorder with Insomnia Symptoms – This condition is characterized by persistent feelings of sadness, hopelessness, and a lack of interest or pleasure in activities, accompanied by difficulties in falling or staying asleep. Individuals may experience changes in appetite, energy levels, and concentration. The insomnia symptoms can exacerbate the depressive symptoms, creating a cycle that can be challenging to break. Over time, the lack of restful sleep can lead to increased irritability and difficulty in managing daily tasks. The disorder can vary in intensity and duration, with some individuals experiencing more severe symptoms than others.

Trial ID:
2023-509070-36-00
Protocol code:
42847922MDD3003
Trial Phase:
Therapeutic confirmatory (Phase III)

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