Otsuka CYPRESS PTSD Trial

Otsuka CYPRESS PTSD Trial

Currently Enrolling!

If you’ve experienced or witnessed a traumatic event and now have unwanted memories of the event, struggle with fear and anxiety, feel isolated from family and friends; or avoid situations that remind you of the trauma, you may have post-traumatic stress disorder (PTSD).

Individuals that meet requirements:

  • Are 18 to 65 years of age
  • Have had PTSD symptoms for at least 6 months prior to this study

All study-related visits, tests, and drugs will be provided at no cost. In addition, reimbursement for study-related travel may be provided.

Otsuka RELAPSE

Otsuka RELAPSE

Currently Enrolling!

If you have major depressive disorder (MDD) and are in a current depressive episode, we invite you to learn about a clinical trial of an investigational drug that is taken with your current antidepressant medication. In this trial, researchers will evaluate the safety and efficacy of the investigational drug as an add-on therapy to your current antidepressant medication. If you meet the requirements listed below, contact us to get more information.

Individuals that meet requirements:

  • Are 18 to 65 years of age
  • Have been diagnosed with recurrent MDD
  • Are in a current major depressive episode for at least the last 8 weeks
  • Have unsatisfactory improvement in symptoms of depression with current treatment

GAIN Alzheimer's Trial

Currently Enrolling!

GAIN is a clinical trial evaluating whether an investigational oral drug is safe and can halt the progression of Alzheimer’s disease by reducing the damage caused by bacteria in the brain.

Individuals that meet requirements:

  • Are age 55-80
  • Have been diagnosed with mild-to-moderate Alzheimer’s disease
  • Have a caregiver or family member who will attend study visits, report on daily activities and oversee you taking medication

Axsome Therapeutics, inc. ADVANCE

Currently Enrolling!

Many individuals with Alzheimer’s Dementia may experience agitation in addition to memory and cognitive difficulties. If you or someone you know is struggling with symptoms of agitation, the ADVANCE study may be a good option for you. The purpose of this clinical trial is to evaluate the efficacy and safety of an investigational product for symptoms of agitation in those with Alzheimer’s.

Individuals that meet requirements:

  • Are male or female, 65-90 years old
  • Have a diagnosis of probable Alzheimer’s Dementia alongside symptoms of agitation
  • Must have an available caregiver
  • Currently take medication for Alzheimer’s (e.g., Donepezil, Memantine)

CHICKADEE Adolescent Females (under 18)

Currently Enrolling!

The Chickadee Study is a research study in teens with postpartum depression (PPD). You may qualify if you are 15 to 17 years old and have had a baby in the last six months.

Individuals that meet requirements:

  • Adolescent females 17 years of age or younger
  • Have given birth within the last 6 months
  • Frequently feel extremely sad, anxious, or overwhelmed, and these symptoms are associated with PPD
  • Have symptoms that began no earlier than the third trimester and no later than the first four weeks following delivery
  • Be willing to temporarily cease breastfeeding for 7 days

No Longer Enrolling

Axsome Therapeutics, Inc

Individuals with Major Depressive Disorder (MDD) may have failed one or more anti-depressant in the past. Axsome is investigating the efficacy of a product in those who have treatment resistant MDD (STRIDE study). If you suffer from Major Depression and have not found success in one or more anti-depressant medications, you may qualify for AXSOME’S STRIDE study!  

Eisai DELPHIA Dementia with Lewy Bodies

The Delphia study will test an investigational medication to see if it might improve cognitive function, including attention, memory, and language in patients who have dementia with Lewy bodies (DLB).

Evaluating Gait and Balance in Subjects with Dementia

Several researchers have found that individuals diagnosed with dementia have a higher likelihood of experiencing episodes of falling or issues with balance. This study examined the effects of intepirdine (RVT-101) on gait and balance in individuals with Alzheimer’s Disease, Lewy Body Dementia, or Parkinson’s Dementia. More information about this study and its results can be found below by clicking on the following link(s). 

Hummingbird Postpartum Depression Trial

The Hummingbird study evaluated an investigational medication in women with moderate to severe postpartum depression. Postpartum depression is a biological complication of pregnancy, including symptoms of sadness, anger, loss of pleasure, and cognitive, emotional, physical symptoms.  Over 100 women participated in the Hummingbird study across 22 states in the U.S. and over 40 different study sites. More information about the trial can be found below from the following link(s).

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Mindset Study

MINDSET is phase II clinical research program that evaluated the investigational medication, RVT-101, for the treatment of mild-to-moderate Alzheimer’s Disease. Researchers investigated the efficacy of combining RVT-101 with Donepezil in cognitive abilities and performance on activities of daily living. This worldwide research trial enrolled over 1,000 participants across hundreds of research sites. More information on the MINDSET study can be found by clicking the link(s) below. 

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PrecisionMed Trial

This study involved administering several cognitive tests on individuals 50 years and older who have a diagnosis of Mild Alzheimer’s Disease or Mild Cognitive Impairment.

Reverse-SD

Those who have symptoms of cognitive declines, such as issues with thinking, judgment, or memory, may be experiencing Mild Cognitive Impairment (MCI) or have already been diagnosed with MCI. This clinical trial is evaluating an investigational drug for those who are experiencing MCI, or mild Alzheimer’s Dementia.

Results from Phase 2a clinical studies in patients with Early-Stage Alzheimer’s disease have been completed.

Sage Therapeutics Robin Study - Females 18 - 45

This research study is evaluating the efficacy and safety of an investigational oral medication in adult women from 18 to 45 with Postpartum Depression. An investigational medication is a study drug that will be tested during a study to see if it is safe and effective for a specific condition and/or group of people.

Shoreline Study

The Shoreline Study is evaluating an investigational oral medication to see if it reduces symptoms of moderate-to-severe depression.

Sprites Study

The SPRITES study examined how sertraline or psychotherapy affects aspects of cognitive, emotional, and physical development in children who are diagnosed with an anxiety, depressive, or obsessive-compulsive disorder.  In addition, the study examined the long-term effects that sertraline may or may not have on children and adolescent development. If you would like to learn more about this study, please click the link(s) below. 

Suvn Life Sciences Ltd.

This is a phase 2a, proof-of-concept, 26-week, double-blind, multicenter, randomized, parallel group, placebo-controlled study to compare the efficacy and safety of treatment with SUVN-502 to placebo treatment in subjects from 50-85 years of age with moderate Alzheimer’s disease receiving stable doses of donepezil HCl and memantine HCl.

Teens and Young Adults Depression Study

This study examined the safety and efficacy for a non-drug therapy (i.e., NeuroStar TMS therapy) for teens or young adults suffering from depression. Study participants received the non-invasive, TMS treatment for no-cost. This non-drug treatment has been FDA-cleared for adults (22-70 years old). If you are interested in reading about the results of this study, or wish to know more information about NeuroStar TMS therapy for the treatment of depression, please click the link(s) below.

Find Out More

Please call or email Anchor Neuroscience research staff if you are interested in learning more about studies for which you may quality or to be placed on our list of potential study subjects.