Citalopram
Regulatory milestones approvals, filings & regulatory actions · 1 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Approved | US (FDA) | CELEXA | — | 1998-07-17 | fda.gov ↗ |
Trials 100 · started per year
Also used as a comparator or background therapy in 95 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 04 trials | ||||||
| Phase 0 | NCT03607331 Comparator | Sep 2018 → Jul 2019 | depressive disorder | China Academy of Chinese Medical Sciences | Unknown | No outcome recorded |
| Phase 0 | NCT03282110 Comparator | Nov 2017 → Jun 2018 | neurotic depression | China Academy of Chinese Medical Sciences | Unknown | No outcome recorded |
| Phase 0 | NCT04846829 Comparator | Apr 2017 → Apr 2028 expected | major depressive disorder | University of California, Los Angeles | Active not recruiting | No outcome recorded |
| Phase 0 | NCT01725048 Comparator | Jan 2011 → May 2012 | major depressive disorder, neoplasm | UNC Lineberger Comprehensive Cancer Center | Completed | No outcome recorded |
| Phase 17 trials | ||||||
| Phase 1 | NCT06192589 Comparator | Feb → Sep 2024 | drug-induced liver injury | Food and Drug Administration (FDA) | Completed | No outcome recorded |
| Phase 1 | NCT03516604 Comparator | May 2018 → Jul 2022 | depressive disorder | University of Oxford | Completed | No outcome recorded |
| Phase 1 | NCT01657760 Comparator | May 2014 → Aug 2017 | alcohol dependence | VA Office of Research and Development | Completed | No outcome recorded |
| Phase 1 | NCT01396720 Comparator | Sep 2011 → Dec 2012 | — | Hadassah Medical Organization | Completed | No outcome recorded |
| Phase 1 | NCT01367756 Background | May → Sep 2011 | — | Hoffmann-La Roche | Completed | No outcome recorded |
| Phase 1 | NCT01424384 Comparator | Sep 2008 → Apr 2009 | mixed anxiety and depressive disorder | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT00676039 Comparator | Nov 2007 → Jul 2008 | — | University of Ottawa | Completed | No outcome recorded |
| Phase 1/22 trials | ||||||
| Phase 1/2 | NCT05271084 Background | Nov 2021 → Feb 2022 | major depressive disorder | Hawler Medical University | Completed | No outcome recorded |
| Phase 1/2 | NCT00612807 Background | Jul 2006 → Jun 2010 | major depressive disorder | Duke University | Completed | No outcome recorded |
| Phase 213 trials | ||||||
| Phase 2 | NCT03321526 Background | Dec 2017 → Jun 2019 | major depressive disorder | Janssen Research & Development, LLC | Completed | No outcome recorded |
| Phase 2 | NCT01937182 Comparator | Sep 2013 → Dec 2016 | ischemic stroke | University of Aarhus | Completed | No outcome recorded |
| Phase 2 | NCT01742832 Comparator | May 2013 → Mar 2016 | major depressive disorder | University of Chicago | Completed | No outcome recorded |
| Phase 2 | NCT01254305 Comparator | Apr 2011 → Jul 2012 | major depressive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 2 | NCT01535573 Comparator | Dec 2010 → Jul 2016 | cocaine dependence | Joy Schmitz | Completed | No outcome recorded |
| Phase 2 | NCT01189812 Comparator | Mar 2010 → Jan 2011 | borderline personality disorder, dysthymic disorder, major depressive disorder | Columbia Northwest Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT01179568 Comparator | Mar 2010 → Feb 2015 | — | New York State Psychiatric Institute | Completed | No outcome recorded |
| Phase 2 | NCT00854100 Background | Jun 2009 → Dec 2010 | major depressive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 2 | NCT00977353 Comparator | Apr 2009 → Jul 2011 | major depressive disorder | China Medical University Hospital | Completed | No outcome recorded |
| Phase 2 | NCT00794040 Comparator | Nov 2008 → Feb 2018 | attention deficit-hyperactivity disorder, disruptive behavior disorder, mood disorder | National Institute of Mental Health (NIMH) | Completed | No outcome recorded |
| Phase 2 | NCT00692445 Comparator | Jun 2008 → May 2009 | major depressive disorder | Targacept Inc. | Completed | No outcome recorded |
| Phase 2 | NCT00672659 Comparator | Feb 2008 → Jan 2009 | major depressive disorder | PharmaNeuroBoost N.V. | Completed | No outcome recorded |
| Phase 2 | NCT00774813 Comparator | Oct 2007 → May 2008 | depressive disorder | Kalaco Scientific, Inc. | Completed | No outcome recorded |
| Phase 2/33 trials | ||||||
| Phase 2/3 | NCT04777838 Comparator | Mar → May 2021 | myofascial pain syndrome, temporomandibular joint disorder | University of Coimbra | Unknown | No outcome recorded |
| Phase 2/3 | NCT01109030 Comparator | Apr 2010 → Oct 2011 | major depressive disorder | Tehran University of Medical Sciences | Completed | No outcome recorded |
| Phase 2/3 | NCT00562861 Comparator | Nov 2007 → Jul 2014 | bipolar depression | Tufts Medical Center | Completed | No outcome recorded |
| Phase 314 trials | ||||||
| Phase 3 | NCT06025474 Comparator | Jan → Oct 2023 | burning mouth syndrome | Federico II University | Unknown | No outcome recorded |
| Phase 3 | NCT04476030 Background | Nov 2020 → Oct 2021 | major depressive disorder | Biogen | Completed | No outcome recorded |
| Phase 3 | NCT03538691 Background | Jul 2018 → Jul 2022 | major depressive disorder | Otsuka Pharmaceutical Development & Commercialization, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02624102 Background | Sep 2015 → Dec 2017 | major depressive disorder | Hemanny, Curt, M.D. | Completed | No outcome recorded |
| Phase 3 | NCT02400346 Background | Mar 2015 → Jun 2016 | major depressive disorder | H. Lundbeck A/S | Completed | No outcome recorded |
| Phase 3 | NCT02279953 Background | Oct 2014 → Apr 2016 | major depressive disorder | H. Lundbeck A/S | Completed | No outcome recorded |
| Phase 3 | NCT01838876 Background | Apr 2013 → Jul 2015 | major depressive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 3 | NCT01715805 Background | Nov 2012 → Jun 2016 | major depressive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 3 | NCT02179268 Comparator | Mar 2012 → Apr 2014 | osteoporosis | Guiyang Medical University | Completed | No outcome recorded |
| Phase 3 | NCT01312922 Comparator | Sep 2011 → Nov 2012 | major depressive disorder | PharmaNeuroBoost N.V. | Completed | No outcome recorded |
| Phase 3 | NCT00351910 Background | May 2006 → Apr 2007 | major depressive disorder | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00074815 Background | Sep 2003 → Nov 2009 | obsessive-compulsive disorder | Duke University | Completed | No outcome recorded |
| Phase 3 | NCT00067301 Background | Sep 2003 → Apr 2007 | major depressive disorder | National Center for Complementary and Integrative Health (NCCIH) | Completed | No outcome recorded |
| Phase 3 | NCT00044798 Background | Sep 2001 → Mar 2007 | depressive disorder | University of Iowa | Completed | No outcome recorded |
| Phase 431 trials | ||||||
| Phase 4 | NCT07047651 Background | Jun 2025 → Dec 2027 expected | treatment-refractory schizophrenia | Dr. Stavroula Rakitzi | Active not recruiting | No outcome recorded |
| Phase 4 | NCT06740188 Comparator | Jan 2025 → Dec 2026 expected | — | Tongji University | Recruiting | No outcome recorded |
| Phase 4 | NCT07113145 Comparator | Jun 2024 → Jan 2025 | premature ejaculation | Beni-Suef University | Completed | No outcome recorded |
| Phase 4 | NCT05735756 Comparator | Jan → Apr 2022 | — | Academic Medical Center - University of Amsterdam | Terminated | No outcome recorded |
| Phase 4 | NCT05148169 Background | Jan 2020 → Dec 2022 | major depressive disorder | Shanghai Mental Health Center | Unknown | No outcome recorded |
| Phase 4 | NCT04975724 Background | Apr 2019 → Oct 2025 | major depressive disorder | Fidia Farmaceutici s.p.a. | Unknown | No outcome recorded |
| Phase 4 | NCT03779789 Comparator | Feb 2019 → Feb 2023 | major depressive disorder | Azienda Ospedaliera Universitaria Integrata Verona | Completed | No outcome recorded |
| Phase 4 | NCT02386475 Comparator | Jan 2015 → Mar 2017 | stroke disorder | Hospital de Granollers | Completed | No outcome recorded |
| Phase 4 | NCT02825342 Comparator | Mar 2014 → Aug 2017 | myocardial infarction | Evangelismos Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT02022709 Comparator | Jan 2014 → Nov 2017 | obsessive-compulsive disorder | Shanghai Mental Health Center | Completed | No outcome recorded |
| Phase 4 | NCT01903447 Comparator | Dec 2013 → Feb 2018 | anxiety | University of Illinois at Chicago | Completed | No outcome recorded |
| Phase 4 | NCT02028026 Comparator | Apr 2013 → Feb 2015 | anxiety, major depressive disorder | Massachusetts General Hospital | Withdrawn | No outcome recorded |
| Phase 4 | NCT03278938 Comparator | Jun 2012 → Jan 2016 | depressive disorder | New York State Psychiatric Institute | Withdrawn | No outcome recorded |
| Phase 4 | NCT01764867 Comparator | Jun 2012 → Oct 2014 | major depressive disorder | Shanghai Mental Health Center | Unknown | No outcome recorded |
| Phase 4 | NCT01460212 Comparator | Dec 2011 → Dec 2014 | major depressive disorder | Nanjing Medical University | Unknown | No outcome recorded |
| Phase 4 | NCT01473381 Comparator | Dec 2011 → Jun 2013 | major depressive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 4 | NCT01658228 Background | Sep 2011 → Jan 2016 | cognitive impairment with or without cerebellar ataxia, depressive disorder | New York State Psychiatric Institute | Completed | No outcome recorded |
| Phase 4 | NCT01032083 Comparator | Jul 2011 → Dec 2014 | schizophrenia | Imperial College London | Completed | No outcome recorded |
| Phase 4 | NCT01919216 Comparator | Jan 2010 → Jun 2016 | major depressive disorder | New York State Psychiatric Institute | Completed | No outcome recorded |
| Phase 4 | NCT01305707 Comparator | Jul 2009 → Jul 2014 | major depressive disorder | Hospital Universitari de Bellvitge | Terminated | No outcome recorded |
| Phase 4 | NCT00834834 Comparator | Mar 2009 → Aug 2015 | borderline personality disorder | New York State Psychiatric Institute | Completed | No outcome recorded |
| Phase 4 | NCT01300364 Comparator | Nov 2008 → Dec 2011 | schizophrenia | Fundació Sant Joan de Déu | Unknown | No outcome recorded |
| Phase 4 | NCT00955474 Comparator | Sep 2008 → Jan 2013 | major depressive disorder | Massachusetts General Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT00594269 Comparator | Aug 2008 → Dec 2010 | dementia | Innlandet Hospital Trust | Completed | No outcome recorded |
| Phase 4 | NCT00666757 Comparator | May 2008 → Feb 2009 | depressive disorder | Eli Lilly and Company | Completed | No outcome recorded |
| Phase 4 | NCT00602290 Comparator | Feb 2008 → Jan 2013 | depressive disorder | University of California, Los Angeles | Completed | No outcome recorded |
| Phase 4 | NCT00825825 Comparator | May 2007 → Apr 2011 | — | Michael Henry, MD | Completed | No outcome recorded |
| Phase 4 | NCT00680602 Comparator | Jan 2006 → Sep 2008 | obsessive-compulsive disorder | University of Sao Paulo | Completed | No outcome recorded |
| Phase 4 | NCT00254020 Background | Jun 2005 → Jan 2011 | depressive disorder | Sunnybrook Health Sciences Centre | Completed | No outcome recorded |
| Phase 4 | NCT00221494 Background | Jan 2004 → Jun 2006 | depressive disorder | Mark Frye | Withdrawn | No outcome recorded |
| Phase 4 | NCT00047671 Comparator | Jun 2002 → Nov 2006 | depressive disorder | National Institute of Mental Health (NIMH) | Completed | No outcome recorded |
| Phase not applicable21 trials | ||||||
| — | NCT05957094 Comparator | Aug 2023 → Aug 2024 | depressive disorder, metabolic disease involving other neurotransmitter deficiency | University of British Columbia | Unknown | No outcome recorded |
| — | NCT06358014 Background | May 2023 → Dec 2024 | depressive disorder | Xiao Wang | Unknown | No outcome recorded |
| — | NCT05832619 Background | Nov 2022 → Dec 2025 | major depressive disorder | Xiaomei Shao | Unknown | No outcome recorded |
| — | NCT05720637 Background | Nov 2022 → Jan 2024 | major depressive disorder | Xiaomei Shao | Completed | No outcome recorded |
| — | NCT05528224 Background | Sep 2022 → Aug 2023 | obsessive-compulsive disorder | Shanghai Mental Health Center | Terminated | No outcome recorded |
| — | NCT05605002 Background | Jan 2022 → Dec 2025 | major depressive disorder | Xiaomei Shao | Unknown | No outcome recorded |
| — | NCT05588102 Background | May 2021 → May 2023 | cognitive disorder | Capital Medical University | Completed | No outcome recorded |
| — | NCT03558256 Background | May 2016 → Dec 2018 | major depressive disorder | Shanghai Mental Health Center | Unknown | No outcome recorded |
| — | NCT02655354 Background | Oct 2015 → Nov 2019 | alcohol-related disorders, brain injury, cognitive impairment with or without cerebellar ataxia, depressive disorder +1 | University of Washington | Completed | No outcome recorded |
| — | NCT02262156 Comparator | Aug → Oct 2014 | depressive disorder, temporal lobe epilepsy | El Instituto Nacional de Neurologia y Neurocirugia Manuel Velasco Suarez | Completed | No outcome recorded |
| — | NCT01944657 Comparator | Sep 2013 → Dec 2015 | major depressive disorder | Sheppard Pratt Health System | Withdrawn | No outcome recorded |
| — | NCT01896349 Background | Apr 2013 → Aug 2014 | — | Hospital de Clinicas de Porto Alegre | Unknown | No outcome recorded |
| — | NCT04355455 Comparator | Jul → Dec 2011 | gastroesophageal reflux disease | Universitaire Ziekenhuizen KU Leuven | Completed | No outcome recorded |
| — | NCT01831440 Background | Jan 2011 → Jan 2014 | depressive disorder | Nanjing Medical University | Unknown | No outcome recorded |
| — | NCT01946607 Comparator | Jul 2009 → Nov 2010 | — | University of Oxford | Completed | No outcome recorded |
| — | NCT00944996 Comparator | Jun 2009 → Jun 2010 | major depressive disorder | Tirat Carmel Mental Health Center | Completed | No outcome recorded |
| — | NCT00564278 Background | Feb 2008 → Aug 2013 | depressive disorder | New York State Psychiatric Institute | Completed | No outcome recorded |
| — | NCT00129467 Background | Feb 2005 → Sep 2009 | cancer, depressive disorder | US Department of Veterans Affairs | Completed | No outcome recorded |
| — | NCT00226694 Comparator | Sep 2003 → Aug 2011 | alcohol dependence | University of Cincinnati | Completed | No outcome recorded |
| — | NCT00048815 Comparator | Feb 2003 → Apr 2007 | depressive disorder | Massachusetts General Hospital | Completed | No outcome recorded |
| — | NCT00047450 Comparator | Sep 2001 → Sep 2006 | schizophrenia | Veterans Medical Research Foundation | Completed | No outcome recorded |
Evidence & citations 16 cited values
Every value below carries the sentence it was read from. 198 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Citalopram | “we have restricted the IMPACT list of antidepressants to SSRIs (sertraline, escitalopram, paroxetine, fluoxetine, citalopram), duloxetine, bupropion, and mirtazapine. These...” NCT02458690 ↗190“Participants receive only clinical routine antidepressant treatment,Which include fluoxetine (Prozac); sertraline (Zoloft); paroxetine (Paxil); citalopram (Celexa)...” NCT01831440 ↗ “Antidepressant medications may include the following: citalopram (Celexa), escitalopram (Lexapro), paroxetine (Paxil CR), sertraline (Zoloft), venlafaxine XR (Effexor XR),...” NCT00564278 ↗ “Medication group is a control group that can choose to use the serotonin reuptake inhibitors (SSRIs) approved by China food and Drug Administration (SFDA) for the treatment of...” NCT03558256 ↗ “ADT such as citalopram, escitalopram, fluoxetine, sertraline, paroxetine, vilazodone, venlafaxine, desvenlafaxine, duloxetine or bupropion prescribed in accordance with its...” NCT01838876 ↗ “Citalopram, ecitalopram, fluoxetine, sertraline, paroxetine IR, paroxetine CR, venlafaxine IR, venlafaxine XR (extended release), desvenlafaxine, duloxetine, mirtazapine,...” NCT02400346 ↗ “Drug: Antidepressant (citalopram, duloxetine, escitalopram, sertraline, or venlafaxine XR) + cariprazine (0.1-0.3 mg/d) Oral, once daily for 8 weeks following an 8 week...” NCT00854100 ↗ “The dose is 20-60mg/day for fluoxetine, 20-40mg/day for paroxetine, 100-300mg/day for fluvoxamine, 50-200mg/day for sertraline, 20-40mg/day for citalopram, 10-20mg/day for...” NCT05148169 ↗ “Participants will receive SSRI antidepressant (such as, citalopram, escitalopram, fluvoxamine, fluoxetine, paroxetine, sertraline, vilazodone or vortioxetine) as a part of...” NCT03321526 ↗ “Antidepressant medications may include any of the following: citalopram, escitalopram, paroxetine, sertraline, venlafaxine XR, bupropion SR, duloxetine, nortriptyline, and mirtazapine.” NCT00742573 ↗ “approved by the State Food and Drug Administration (CFDA) for the treatment of OCD (i.e., fluoxetine, paroxetine, sertraline and fluvoxamine) as well as citalopram and escitalopram” NCT05528224 ↗ “SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist. Once daily for 6 weeks.” NCT05832619 ↗ “quantifying the range of concentration to citalopram, escitalopram, sertraline, fluoxetine, paroxetine, fluvoxamine, duloxetine and venlafaxine in mother plasma and breast milk” NCT01796132 ↗ “This study uses SSRIs class drugs, including fluoxetine, paroxetine, fluvoxamine, sertraline, citalopram, and escitalopram, with no specific restrictions on the type of drugs.” NCT06358014 ↗ “ADT such as bupropion, citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, sertraline, venlafaxine, paroxetine or vilazodone as prescribed by the physician.” NCT01715805 ↗ “Throughout the study, all subjects will receive either escitalopram (Lexapro) or citalopram (Celexa) on the basis of the study doctor's clinical judgment.” NCT00361218 ↗ “SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist.” NCT05720637 ↗ “SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist.” NCT05605002 ↗ “Patients who are not on a SSRI at the time of enrollment will be prescribed citalopram 10 mg per day for 2 weeks, then 20 mg per day.” NCT00129467 ↗ “Patients with MDD, in use of antidepressants (fluoxetine, citalopram, escitalopram, bupropion, etc.) without psychotherapy.” NCT02624102 ↗ “Received Citalopram hydrobromide, starting with 10 mg once daily for 1 week, followed by 20 mg once daily for 10 weeks” NCT07113145 ↗ “SSRIs (daily dose of at least 20 mg for citalopram, 20 mg for fluoxetine, 100 mg for sertraline, 20 mg for paroxetine)” NCT00612807 ↗ “selective serotonin reuptake inhibitors (fluoxetine, sertraline, citalopram, escitalopram, paroxetine or fluvoxamine)” NCT03993535 ↗ “sertraline: 100-200mg, citalopram 20-40mg, escitalopram 10-20mg, paroxetine 20-60mg; fluoxetine 20-80mg” NCT01903447 ↗ “Patients will receive the "treatment as usual" with a SSRI: sertraline or citalopram.” NCT02262156 ↗ “selective serotonin reuptake inhibitor (SSRI; paroxetine or citalopram; n = 34)” PMID 26663632 ↗ Dec 2015 “Fluoxetine, escitalopram, citalopram, fluvoxamine, or sertraline” NCT03222570 ↗ “paroxetine, fluoxetine, sertraline, escitalopram, citalopram” NCT00944996 ↗ “either citalopram 20 mg/day or fluvoxamine 100 mg/day” PMID 25689244 ↗ Feb 2015 “citalopram (20 mg, increased to 30 to 40 mg)” NCT00118430 ↗ “paroxetine (Paxil); citalopram (Celexa)” NCT01460212 ↗ “escitalopram, citalopram or sertraline” NCT02279953 ↗ “- Citalopram 20-60 mg/d. N06AB04” NCT01305707 ↗ “citalopram (Celexa and others)” NCT01944657 ↗ “Citalopram (Celexa)10-60;” NCT00074815 ↗ “citalopram 20-60mg/day” NCT02023567 ↗ “Citalopram, Celexa” NCT01916824 ↗ “citalopram_Celexa” NCT00817011 ↗ “Citalopram” NCT00864890 ↗ “Citalopram” NCT00865085 ↗ “citalopram” NCT00157547 ↗ |
| Known as | Celexa | “Participants receive only clinical routine antidepressant treatment,Which include fluoxetine (Prozac); sertraline (Zoloft); paroxetine (Paxil); citalopram (Celexa)...” NCT01831440 ↗16“Antidepressant medications may include the following: citalopram (Celexa), escitalopram (Lexapro), paroxetine (Paxil CR), sertraline (Zoloft), venlafaxine XR (Effexor XR),...” NCT00564278 ↗ “This study will evaluate the effectiveness of the stimulant medication methylphenidate (MPH, more commonly known as Ritalin ) when combined (or not combined) with the...” NCT00794040 ↗ “Throughout the study, all subjects will receive either escitalopram (Lexapro) or citalopram (Celexa) on the basis of the study doctor's clinical judgment.” NCT00361218 ↗ “METHOD: Effexor XR/Novo-venlafaxine XR 75 mg and Celexa/Gen-citalopram 40 mg were studied in a randomized crossover design.” PMID 19653973 ↗ Jul 2009 “This study will compare the safety and effectiveness two medications, citalopram (Celexa®) and risperidone (Risperdal®).” NCT00073658 ↗ “We will administer MDMA alone and in combination with the antidepressant citalopram (one trade name for this is Celexa).” NCT00838305 ↗ “antidepressant therapy with Celexa (Citalopram) in people suffering from Major Depressive Disorder.” NCT00067301 ↗ “Participants receive citalopram (Celexa) for 8 weeks and a placebo for 1 week.” NCT00047671 ↗ “Participants will take citalopram (Celexa)” NCT00047450 ↗ “citalopram hydrobromide (Celexa®) tablets” NCT03538691 ↗ “citalopram (Celexa and others)” NCT01944657 ↗ “Citalopram (Celexa)10-60;” NCT00074815 ↗ “Citalopram [Celexa]” NCT00009204 ↗ “citalopram (celexa)” NCT00254007 ↗ “citalopram_Celexa” NCT00817011 ↗ |
| Known as | CelexaTM | “CelexaTM 40 mg tablets, single dose” NCT00865085 ↗ |
| Known as | cipralex | “citalopram (cipralex)” NCT00532519 ↗ |
| Known as | Cipramil | “50 patients with reflux hypersensitivity and 50 patients with functional heartburn will receive either placebo or citalopram (Cipramil®) 20 mg as an add-on for a period of 8 weeks.” NCT03499171 ↗ |
| Known as | CIT | “OBJECTIVE: To confirm the efficacy of a targeted complicated grief treatment (CGT), determine whether citalopram (CIT) enhances CGT outcome, and examine CIT efficacy without CGT.” PMID 27276373 ↗ Jul 20161“Pipamperone/Citalopram (PNB01) Versus Citalopram (CIT) and Versus Pipamperone (PIP) in Major Depressive Disorder (MDD)” NCT01312922 ↗ |
| Known as | Citalopram Aurobindo | “The medicinal product Citalopram Aurobindo contains citalopram as active ingredient available on the market in 20 mg film coated tablets. The tablets are divisible in two equal...” NCT04975724 ↗ |
| Known as | Citalopram HBr | “Citalopram HBr eq. 10 mg tablets, single dose” NCT00865943 ↗2“Citalopram HBr 40 mg tablets, single dose” NCT00865085 ↗ “Citalopram HBr 40 mg tablets, single dose” NCT00864890 ↗ |
| Known as | Citalopram hydrobromide | “Citalopram Hydrobromide Tablets 40 mg: Test Product: Citalopram Hydrobromide Tablets 40 mg manufactured by Torrent Pharmaceuticals Limited, India” NCT00940238 ↗5“the control group was given citalopram hydrobromide combined with zolpidem” NCT06740188 ↗ “citalopram hydrobromide (Celexa®) tablets” NCT03538691 ↗ |
| Known as | Citalopram, Celexa | “citalopram (Celexa)” NCT01460212 ↗1“Citalopram, Celexa” NCT01916824 ↗ |
| Known as | CTP | “OBJECTIVE: Despite the clinical importance of chronic and severe irritability, there is a paucity of controlled trials for its pharmacological treatment. Here, we examine the...” PMID 31128268 ↗ May 2019 |
| Known as | Gen-Citalopram | “METHOD: Effexor XR/Novo-venlafaxine XR 75 mg and Celexa/Gen-citalopram 40 mg were studied in a randomized crossover design.” PMID 19653973 ↗ Jul 2009 |
| Known as | seropram | ClinicalTrials.gov intervention name — accepted as the source's own label NCT07047651 ↗ |
| Action | Inhibit | “citalopram, a selective serotonin reuptake inhibitor (SSRI)” NCT00217828 ↗ |
| Modality | Small molecule | “citalopram, another SSRI” NCT00834834 ↗ |
| Route | Oral | “taken orally” NCT00048815 ↗ |