Purpose

The purpose of this study is to determine if treatment with a single dose of RE104 for Injection reduces depressive symptoms or depressive symptoms mixed with anxiety symptoms in participants with Adjustment Disorder due to cancer or other illnesses such as Amyotrophic Lateral Sclerosis (ALS), Multiple Sclerosis (MS), Parkinson's Disease (PD) or Idiopathic Pulmonary Fibrosis (IPF) as compared to active-placebo.

Condition

Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Has a ≥4 week history of AjD as defined by DSM-5-TR with either depressed mood, or mixed anxiety and depressed mood confirmed by clinical interview with evidence that the AjD was instigated by one of the following medical illnesses (e.g., diagnosis, impact, management, recurrence, prognosis): Cancer, ALS, MS, PD or IPF - Is sufficiently ambulatory and capable of self care as necessary to complete study procedures - Has normal cognitive function - Is on stable use of antidepressants or psychotherapy, or is willing to delay use until the end of study - If female is not pregnant or planning to become pregnant. If male is not planning to make a partner pregnant - Is willing and able to comply with the conditions and requirements of the study

Exclusion Criteria

  • Has a significant risk of suicide - Has active or medical history of bipolar disorder, schizophrenia, schizoaffective disorder, psychotic disorder and/or borderline personality disorder, or first-degree family history of psychosis or bipolar disorder - Has active or a history of central nervous system malignancy - Has other medically significant conditions rendering unsuitability for the study - Has used or will need to use prohibited medications or therapies - Has a known sensitivity or intolerance to study intervention or potential rescue medications

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Active Comparator
1.5 mg RE104
A single subcutaneous injection of 1.5 mg RE104 for Injection
  • Drug: RE104 for Injection
    Single, subcutaneous dose of RE104 for Injection
Experimental
30 mg RE104
A single subcutaneous injection of 30 mg RE104 for Injection
  • Drug: RE104 for Injection
    Single, subcutaneous dose of RE104 for Injection

Recruiting Locations

UAB, Psychiatry and Behavioral Neurology
Birmingham 4049979, Alabama 4829764 35209
Contact:
Seher Premani
205-996-1198
spremani@uab.edu

More Details

Status
Recruiting
Sponsor
Reunion Neuroscience Inc

Study Contact

Mark Pollack, Chief Medical Officer
1-888-880-REUN
info@reunionneuro.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.