Post-traumatic Stress Disorder
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Sign up freeTop drugs studied for this disease
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CLINICAL_TRIALS research · 2009-06-03Clinical Trial Update: Forgiveness-Based Writing to Prevent Post-Traumatic Stress Disorder (PTSD) in Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Veterans [NA]
A clinical trial evaluating forgiveness-based writing as a preventive intervention for post-traumatic stress disorder in veterans of OEF/OIF…
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CLINICAL_TRIALS withdrawal · 2009-06-03Clinical Trial Update: Affect Management Group for Adult Survivors of Childhood Trauma [Phase 1]
A Phase 1 trial studying affect management for adult survivors of childhood trauma has been withdrawn.
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CLINICAL_TRIALS trial_result · 2009-04-29Clinical Trial Update: Topiramate in the Treatment of Posttraumatic Stress Disorder in Civilians [Phase 4]
A Phase 4 clinical trial evaluating topiramate for post-traumatic stress disorder in civilians has completed. The document notes the study s…
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FDA approval · 2009-04-21FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Granules Pharmaceuticals Inc.)
FDA approved a supplemental application for sertraline hydrochloride from Granules Pharmaceuticals Inc., indicating approval of a modificati…
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CLINICAL_TRIALS trial_result · 2009-03-05Clinical Trial Update: Stress-Reducing Interventions in HIV+ Patients: Pilot [NA]
A pilot clinical trial at Kent State University is evaluating stress-reducing interventions in people with post-traumatic stress disorder an…
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FDA approval · 2009-02-25FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for sertraline hydrochloride from Aurobindo Pharma Limited, a generic version of the antidepressant …
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FDA approval · 2009-01-30FDA Approved: ZOLOFT — Supplemental Application (ROERIG)
FDA approved a supplemental application for Zoloft (sertraline hydrochloride) submitted by ROERIG.
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FDA approval · 2009-01-30FDA Approved: PAROXETINE HYDROCHLORIDE — Supplemental Application (Apotex Corp)
FDA approved a supplemental application for PAROXETINE HYDROCHLORIDE from Apotex Corp.
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FDA approval · 2009-01-30FDA Approved: PAXIL — Supplemental Application (Apotex Corp)
FDA approved a supplemental application from Apotex Corp for Paxil (paroxetine hydrochloride), authorizing a generic version under the exist…
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CLINICAL_TRIALS trial_result · 2009-01-21Clinical Trial Update: Guanfacine for the Treatment of Post Traumatic Stress Disorder (PTSD) [Phase 1]
This document reports the completion of a Phase 1 clinical trial evaluating guanfacine as a treatment for post-traumatic stress disorder con…
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CLINICAL_TRIALS research · 2009-01-21Clinical Trial Update: Immune and Endocrine Function in Post-Traumatic Stress Disorder
This clinical trial update summarizes findings on immune and endocrine function in people with post-traumatic stress disorder. The study is …
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CLINICAL_TRIALS research · 2009-01-21Clinical Trial Update: Compare the Medical Conditions of Gulf War Veterans to Non-Deployed Veterans
This completed clinical trial compared Gulf War veterans with non-deployed veterans to assess differences in several health conditions. The …
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CLINICAL_TRIALS trial_result · 2009-01-21Clinical Trial Update: Prazosin Treatment for Combat Trauma PTSD (Post-Traumatic Stress Disorder) Nightmares and Sleep Disturbance [Phase 4]
Phase 4 clinical trial evaluating prazosin for combat-related PTSD nightmares and sleep disturbance has completed.
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CLINICAL_TRIALS research · 2009-01-21Clinical Trial Update: Hyporeactivity and Gulf War Illness [NA]
This is a completed clinical trial update from the US Department of Veterans Affairs examining hyporeactivity in Gulf War syndrome and relat…
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CLINICAL_TRIALS trial_result · 2009-01-12Clinical Trial Update: KIDNET Versus Meditation/Relaxation - a Dissemination RCTT for Children in Sri Lanka Traumatized by the War and the Tsunami [Phase 3]
Phase 3 randomized trial comparing KIDNET therapy to meditation/relaxation for children with post-traumatic stress disorder in Sri Lanka aft…
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CLINICAL_TRIALS trial_result · 2009-01-07Clinical Trial Update: Propranolol in Post Traumatic Stress Disorder [Phase 2]
A Phase 2 trial of propranolol for Post-Traumatic Stress Disorder has completed.
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CLINICAL_TRIALS trial_result · 2008-12-12Clinical Trial Update: Prolonged Exposure Therapy Versus Active Psychotherapy in Treating Post-Traumatic Stress Disorder in Adolescents [Phase 1]
A Phase 1 clinical trial comparing Prolonged Exposure Therapy with Active Psychotherapy for adolescents with Post-Traumatic Stress Disorder …
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CLINICAL_TRIALS trial_result · 2008-12-08Clinical Trial Update: Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety [Phase 4]
Phase 4 clinical trial update reporting the completion of a study evaluating Seroquel SR (quetiapine) for alcohol use disorder with comorbid…
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FDA approval · 2008-10-31FDA Approved: PAROXETINE HYDROCHLORIDE — Supplemental Application (Apotex Corp)
FDA approved Apotex Corp's supplemental application for paroxetine hydrochloride (paroxetine HCl), confirming continued approval for the gen…
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FDA approval · 2008-10-31FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (Rising Pharma Holdings, Inc.)
The FDA approved an original generic application for sertraline hydrochloride by Rising Pharma Holdings, Inc., allowing a generic version of…
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FDA approval · 2008-07-16FDA Approved: SERTRALINE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approves a supplemental abbreviated new drug application (ANDA) for sertraline from Heritage Pharmaceuticals d/b/a Avet Pharmaceuticals …
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FDA approval · 2008-07-02FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Lupin Pharmaceuticals, Inc.)
The FDA approved Lupin Pharmaceuticals, Inc.'s supplemental application for sertraline hydrochloride (generic sertraline), authorizing the a…
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FDA approval · 2008-06-25FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for sertraline hydrochloride manufactured by Aurobindo Pharma Limited.
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FDA approval · 2008-05-20FDA Approved: PAROXETINE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for paroxetine hydrochloride/paroxetine from Zydus Lifesciences Limited, authorizing a generic parox…
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CLINICAL_TRIALS trial_result · 2008-03-26Clinical Trial Update: Self-Efficacy Enhancing Interviewing Techniques Study [NA]
A completed clinical trial from the University of California, Davis evaluating self-efficacy–enhancing interviewing techniques in patients w…