MedPath

Efficacy and Safety of Sibutramin-containing Drugs in Patient With Alimentary Obesity

Phase 4
Completed
Conditions
Obesity
Interventions
Registration Number
NCT05821543
Lead Sponsor
Promomed, LLC
Brief Summary

This is Open multicenter randomized Phase IV study to evaluate the efficacy and safety of the drug Reduxin® Forte, film-coated tablets, in comparison with the drug Reduxin®, capsules, in patients with alimentary obesity was conducted in 5 cities of the Russian Federation (St. Petersburg, Ivanovo, Kirov, Samara, Rostov-on-Don) on the basis of 8 research centers.

Detailed Description

Male and female patients (240 people) inclusive with alimentary obesity, meeting the inclusion criteria and not meeting the non-inclusion criteria, were randomized into 2 groups in a 1:1 ratio. One group (n=120) received sibutramine+ metformin p. o., 1 tablet (850 mg + 10 mg) once per day, the second group (n=120) received sibutramine+ microcrystalline cellulose (MCC) p. o., 1 capsule (10 mg + 158.5 mg) once per day in the morning. On day 30 ± 1, in the absence of a 2 kg weight loss compared to the first visit, the dose was increased in accordance with the medical instruction. The therapy period was 180 days.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
240
Inclusion Criteria
  1. Availability of the Informed Consent Form of the Patient Information Leaflet (PIL) signed and dated by patient.

  2. Men and women aged 18 to 65 years inclusive at the time of signing the Informed Consent Form in PIL.

  3. The presence of alimentary obesity.

  4. BMI >30 kg/m2.

  5. Failure of non-pharmacological treatment at the time of screening (weight loss <5% within 3 months of treatment).

  6. Patient consent to change in diet, eating behavior, and increased physical activity, and adherence to the investigator's recommendations throughout participation in the study

  7. Patient's consent to use reliable contraceptive methods through out the study and for 3 weeks after the end of the study. The following people could take part in the study:

    • women who have a negative pregnancy test and use the following contraceptive methods: a barrier method (condom or occlusive cap (diaphragm or cervical/vaulted cap)) or a double barrier method of contraception (condom or occlusive cap). The use of estrogen-containing contraceptives was allowed provided that the drug was used in one dosing regimen for at least 3 months prior to study entry and it was planned to use it at the same dosing regimen throughout the study participation. Women incapable of childbearing may also participate in the study (with past history of: hysterectomy, tubal ligation, infertility, menopause for more than 1 year) or
    • men with preserved reproductive function using barrier contraceptives, as well as men with infertility or a history of vasectomy
Exclusion Criteria
  1. Hypersensitivity to the components of the study drug/comparator drug

  2. Secondary (symptomatic) obesity.

  3. Diabetes mellitus type I or II in history and/or at the time of screening.

  4. Use of a low-calorie (<1600 kcal/day) diet for 3 months prior to screening.

  5. Patients who previously received drugs based on sibutramine.

  6. The use of drugs, herbal remedies or dietary supplements for the treatment of obesity less than 3 months prior to screening.

  7. Use of systemic glucocorticosteroids for less than 3 months prior to screening.

  8. Plan to change current smoking status during the study or quit smoking less than 3 months prior to screening.

  9. The need for surgical treatment of obesity during the study or the history of this treatment.

  10. Impaired liver function (AST and/or ALT ≥ 2 UNL and/or total bilirubin ≥ 1.5 UNL) at the time of screening.

  11. Impaired renal function (creatinine clearance, calculated according to the Cockcroft- Gault formula, less than 45 ml/min) at the time of screening.

  12. Acute conditions in which there was a risk of developing impaired renal function:

    dehydration (with diarrhea, vomiting), severe infectious diseases, shock (at the time of screening).

  13. Cardiovascular diseases (in history and/or at the time of screening): ischemic heart disease (myocardial infarction, angina pectoris), chronic heart failure in the stage of decompensation, occlusive diseases of peripheral arteries, tachycardia (HR> 90 beats/min (mean for 3 measurements)), arrhythmia, cerebrovascular diseases (stroke, transient disorders of cerebral circulation).

  14. Uncontrollable hypertension (blood pressure (BP) >145/90 mm Hg on screening).

  15. History of pulmonary hypertension.

  16. Clinically apparent manifestations of acute and chronic diseases that could lead to the development of tissue hypoxia (including respiratory failure, heart failure).

  17. Hyperthyroidism.

  18. Uncontrolled hypothyroidism at the time of screening (if using thyroid drugs or synthetic thyroid hormones, the drugs must have been used at a stable dose for at least 3 months prior to screening).

  19. Subclinical hypothyroidism at the time of screening.

  20. Benign prostatic hyperplasia (for men) in history.

  21. Pheochromocytoma in history or suspicion of its presence at screening.

  22. Angle-closure glaucoma in history.

  23. Lactic acidosis (in history and at the time of screening).

  24. Chronic alcoholism, acute ethanol poisoning at the time of screening.

  25. Pharmacological and drug dependence in history and / or at the time of screening.

  26. Serious eating disorders (anorexia nervosa, bulimia nervosa).

  27. History of cholelithiasis or presence of symptoms of cholelithiasis within 3 months prior to screening.

  28. History of schizophrenia, schizoaffective disorder, bipolar disorder, or other psychiatric disorder or suspected of having them at the time of screening.

  29. History of suicide attempt.

  30. Syndrome of Gilles de la Tourette (generalized tics) in history.

  31. Major surgery or trauma (associated with a risk to the patient's life) in the last 6 months before screening.

  32. Planned surgery (elective surgery) at the time of screening

  33. Uncontrolled asthma or asthma controlled by steroids.

  34. History of seizures (with the exception of febrile seizures in childhood) or an increased risk of developing seizures.

  35. HIV, viral hepatitis B and/or C, history of active tuberculosis.

  36. The need for the use of drugs from the list of prohibited therapies.

  37. Taking other medications that, in the opinion of the investigator, could affect the course and results of the clinical trial.

  38. History of malignant neoplasms, except for patients who have not been observed for the disease within the last 5 years, patients with completely healed basal cell skin cancer or completely healed carcinoma in situ.

  39. Severe, decompensated or unstable somatic diseases (any disease or condition that threatened the patient's life or worsened the patient's prognosis, and also made it impossible for him to participate in a clinical study).

  40. Patient's unwillingness or inability to comply with procedures of the Study Protocol (in the opinion of the investigator).

  41. Pregnancy or breastfeeding period (for women).

  42. Participation in another clinical trial within 3 months prior to study enrollment.

  43. Other conditions that, in the opinion of the investigator, prevented the inclusion of the patient in the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Reduxin Fortemetformin+sibutramineArm 1 (n=120) received metformin+sibutramine p. o., 1 tablet (850 mg + 10 mg) once per day. On day 30 ± 1, in the absence of a 2 kg weight loss compared to the first visit, the dose was increased in accordance with the medical instruction. The therapy period was 180 days.
Reduxinsibutramine+ microcrystalline celluloseArm 2 (n=120) received sibutramine+ microcrystalline cellulose (MCC) p. o., 1 capsule (10 mg + 158.5 mg) once per day in the morning. On day 30 ± 1, in the absence of a 2 kg weight loss compared to the first visit, the dose was increased in accordance with the medical instruction. The therapy period was 180 days.
Primary Outcome Measures
NameTimeMethod
The rate of achieving >5% weight lossFrom baseline to Visit 13 (study completion, 180 days)

The proportion of patients who had achieved more than 5% weight loss

Secondary Outcome Measures
NameTimeMethod
The dynamic of hip widthFrom baseline to Visit 13 (study completion, 180 days)

The average hip width by every month(cm)

The dynamic of waist / hip measurementsFrom baseline to Visit 13 (study completion, 180 days)

The average value of the ratio waist / hip measurements by every month

Dynamics of lipid profile indicators (TG, total cholesterol, LDL-cholesterol, HDL-cholesterol)From baseline to Visit 13 (study completion, 180 days)

The mean value of triglyceride, total cholesterol, LDL- cholesterol, HDL - cholesterol (mmol/l) by every month

The dynamic of quality of lifeFrom baseline to Visit 13 (study completion, 180 days)

The data obtained using the SF-36 Quality of life questionnaire, the average score of the physical health and psychological health by every month

The dynamic of waist measurementFrom baseline to Visit 13 (study completion, 180 days)

The average waist measurement by every month(cm)

The magnitude of the change in body weightFrom baseline to Visit 13 (study completion, 180 days)

Value of weight change calculated as weight on Visit 13 to baseline (kg)

The frequency of patients who required an increase in the dose of the study / reference drugFrom baseline to Visit 3 (30±1 days)

The proportion of the patients requiring an increase in the study / reference dose

The change in Body Mass Index (BMI)From baseline to Visit 13 (study completion, 180 days)

The average value of the change in BMI (%)

The dynamic of BMIFrom baseline to Visit 13 (study completion, 180 days)

The average value of BMI by every month (kg/m2)

The dynamic of body weightFrom baseline to Visit 13 (study completion, 180 days)

The mean body weight by each two weeks (kg)

Trial Locations

Locations (8)

Ivanovo Clinical Hospital named after Kuvaev

🇷🇺

Ivanovo, Russian Federation

Kirov State Medical University

🇷🇺

Kirov, Russian Federation

Pirogov Russian National Research Medical University

🇷🇺

Moscow, Russian Federation

Avrora Limited Liability Company Principal

🇷🇺

Saint Petersburg, Russian Federation

"Rostov State Medical University" of the Ministry of Health of the Russian Federation

🇷🇺

Rostov-on-Don, Russian Federation

"Clinical hospital "RZD-Medicine" of the city of St. Petersburg"

🇷🇺

Saint Petersburg, Russian Federation

Limited Liability Company "Medica"

🇷🇺

Saint Petersburg, Russian Federation

OrKli Hospital Limited Liability Company

🇷🇺

Saint-Petersburg, Russian Federation

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