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A Randomized, Double-Blind, Parallel-Group, Dose-Controlled Study Evaluating the Safety and Efficacy of RE104 for Injection in the Treatment of Adjustment Disorder in Patients with Cancer and Other Medical Illnesses


Primary Investigator
Silveira, Maria
Status
OPEN TO ACCRUAL
Phase
II
NCT Number
NCT07002034
UM Number
2025.089
Age Group
Adults
Management Group
CTSU - Oncology
Oncology Group
Cancer Control and Prevention
ID (Protocol)
60607
Secondary Protocol No
HUM00276484
Scope
Unspecified
Sponsor Type
Industry

Disease Site
Anus
Breast
Cervix
Colon
Corpus Uteri
Esophagus
Kidney
Larynx
Lip, Oral Cavity and Pharynx
Liver
Lung
Melanoma, Skin
Other Digestive Organ
Other Urinary
Ovary
Pancreas
Prostate
Rectum
Small Intestine
Soft Tissue
Stomach
Thyroid
Urinary Bladder

Summary
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.

Eligibility: 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