A Study of the Efficacy and Safety of Ranquilon Tablets in Patients With Anxiety in Neurasthenia and Adjustment Disorders

Valenta Pharm

Status and phase: Completed; Phase 3

Conditions: Adjustment Disorders; Anxiety; Neurasthenia

Treatments: Drug: Placebo; Drug: Ranquilon

Study type: Interventional

Funder types: Industry

Identifiers

NCT05586789

RAN-03-03-2022

Details and patient eligibility

About

The primary objective of the study is to evaluate the efficacy of Ranquilon, 1 mg tablets, at a dose of 6 mg/day compared to placebo for the treatment of patients with anxiety in neurasthenia and adjustment disorder.

An additional study objective was to evaluate the safety of Ranquilon, 1 mg tablets, at a dose of 6 mg/day compared to placebo in patients with anxiety in neurasthenia and adjustment disorder.

Enrollment: 220 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Men and women between the ages of 18 and 70
2. Presence of written consent to participate in the study in accordance with applicable law
3. Patients with anxiety and diagnoses based on ICD-10 criteria: neurasthenia (F48.0) or adjustment disorder (F43.2)
4. HARS anxiety scores of 18-24
5. Severity of asthenia on the Asthenia Self Assessment Scale (MFI-20) of more than 50 points
6. Hamilton Depression Assessment Scale (HAMD-17) score < 6
7. CGI-s scale score of at least 4
8. Negative pregnancy test for women of preserved reproductive potential
9. Consent to use effective contraception for the duration of the study and 30 days after completion (for women of unresolved reproductive potential and men)
10. Ability to understand the requirements for study participants, to give written consent to participate in the study (including the use and communication of patient health information relevant to the study) and to comply with the procedures of the study protocol

Exclusion criteria

1. Known intolerance to the active ingredient and/or excipients in the study drug/placebo of the study drug
2. Known presence of lactase deficiency, lactose intolerance, glucose-galactose malabsorption or galactose intolerance
3. Patients who require concomitant therapy prohibited in this study (MAO inhibitors, antidepressants, neuroleptics, anxiolytics and sedatives (including herbal), sleeping pills when used on a continuous basis), or have taken these drugs within the last month
4. Established or suspected alcohol/drug use at the time of screening or randomization, and/or a history of alcohol, drug or drug dependence
5. Presence of cancer, including a history of cancer (with the exception of a cured tumor with sustained remission for more than 5 years)
6. Presence of tuberculosis, including a history of tuberculosis
7. The presence of HIV, chronic viral hepatitis B/C, syphilis (including a history), or a positive test for HIV, hepatitis B/C, syphilis at screening
8. Patients with a diagnosis established on the basis of ICD-10 criteria: other anxiety disorders (F41)
9. Schizophrenia, schizoaffective, affective and panic disorders
10. Acute psychosis (endogenous-procedural, organic or somatogenic), including history
11. Organic lesions of the central nervous system of traumatic and alcoholic genesis
12. Postencephalitic syndrome
13. Brain tumors, including in the anamnesis
14. Degenerative diseases of the central nervous system (CNS), in particular, multiple sclerosis
15. Depression, including a history of depression
16. Generalized anxiety disorder, including a history
17. Suicidal thoughts or ideas; a history of suicide attempts
18. Epilepsy, seizures, including a history of seizures
19. Diabetes mellitus at the stage of decompensation
20. Established diagnosis of chronic kidney disease stage 3A or higher, or glomerular filtration rate (GFR) calculated by the Cockcroft-Gault formula = 59 ml/min/1.73 m2 or less
21. Established diagnosis of hepatic failure of any severity, or elevated ALT, AST or total bilirubin, urea >3 times the upper limit of normal values
22. Conditions after major surgical interventions, if less than six months have elapsed since the intervention
23. Chronic heart failure New York Heart Association (NYHA) functional class III-IV
24. Severe, decompensated, or unstable disease (any disease or condition that threatens the patient's life or worsens the patient's prognosis, or makes it impossible to perform a clinical trial in the patient)
25. Pregnant women, women breastfeeding, or women planning to become pregnant during the study and 30 days after study participation ends
26. Refusal by the patient to use approved contraception or to completely abstain from sexual intercourse during the entire period of study participation, beginning at Visit 0, and for 30 days after completion of study participation
27. Patient's current or planned participation in psychological or psychotherapeutic interventions designed to treat an anxiety disorder during the course of the clinical trial
28. Participation in any other clinical trial within 90 days prior to the screening period
29. Lack of willingness to cooperate on the part of the patient
30. Other reasons that, in the opinion of the investigator, prevent the patient from participating in the study or pose an unreasonable risk to the patient

Withdrawal Criteria:

1. Patient's desire to stop participating in the study (withdrawal of informed consent) Each patient has the right to stop participating in the study at any time without giving a reason. Withdrawal from the study will not affect the medical care provided to the patient in the future.
2. A decision by the research physician that the patient should be excluded is in the patient's own best interest
3. Patient refuses to cooperate with the investigator or is undisciplined
4. Causes/occurrence of situations during the study that threaten patient safety (e.g., hypersensitivity reactions, SAE, etc.)
5. Inclusion of a patient in the study with inclusion/inclusion criteria not met (prior to randomization)
6. Significant violation of the treatment regimen A significant violation is defined as a) skipping study drug/placebo for 2 consecutive full days or more, or b) taking, in total, < 80% or >120% of the full course (full course = 168 pills)
7. Positive pregnancy test
8. Confirmed diagnosis of COVID-19
9. Occurrence in the course of the study of other reasons that prevent the study according to the protocol
10. Death of a patient

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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220 participants in 2 patient groups, including a placebo group

Ranquilon

Experimental group

Description:

Study drug Ranquilon, tablets, 1 mg, 2 tablets 3 times a day (daily dose - 6 mg/day), daily, for 28 days

Treatment:

Drug: Ranquilon

Placebo

Placebo Comparator group

Description:

Placebo, tablets, 2 tablets 3 times a day, daily, for 28 days

Treatment:

Drug: Placebo