A Study to Assess the Efficacy and Safety of XC221 in Patients With Mild COVID-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

274 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-26

Study Completion Date

2022-11-14

Brief Summary

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The innovative drug XC221 100 mg tablet is designed for the treatment of COVID-19 (SARS-CoV-2 infection). A multicenter, adaptive, randomized, double-blind, placebo-controlled Phase III clinical study is aimed to assess the efficacy and safety of XC221 100 mg tablet, in mild COVID-19 patients during a 14-days treatment.

The primary objective of the study is to demonstrate the efficacy of XC221 100 mg tablet (200 mg daily dose) in achieving clinical improvement of mild COVID-19 symptoms.

The secondary objective of the study is to evaluate the safety of XC221 100 mg tablet (200 mg daily dose) in mild COVID-19 patients.

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Detailed Description

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8 Russian centers will participate in this study. The trail will consist of three periods: screening (duration not more than 1 day, it may coincide with the randomization visit and beginning of drug administration), treatment period (14 full days) and follow-up period (15 ± 1 days after completion of treatment with XC221 / Placebo). The duration of participation in the study for each patient will be no more than 32 days.

274 eligible patients with confirmed COVID-19 will be randomized into two groups (Group A and Group B) in a 1:1 ratio: Group A - XC221 200 mg daily (137 patients); Group В - Placebo (137 patients).

During the treatment period (14 full days), 1 tablet of XC221 / Placebo will be administered 2 times a day in addition to the standard of care (SoC) for COVID-19 according to The Temporary guidelines for the prevention, diagnosis and treatment of SARS-CoV-2 infection of the Ministry of Health of the Russian Federation (the MoH Temporary Guidelines). The follow-up period will last for 15 ± 1 days.

Conditions

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Sars-CoV-2 Infection

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups (Group A and Group B) in a 1:1 ratio: Group A - investigational product; Group В - Placebo.

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Tablets identical in terms of composition, appearance and labeling to XC221 tablets, but without active substance will be used as Placebo.

Study Groups

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XC221

XC221 100 mg orally. 1 tablet of XC221 100 mg 2 times a day during 14 full days of treatment period

Group Type EXPERIMENTAL

XC221

Intervention Type DRUG

Participants will receive XC221 100 mg 2 times a day during 14 full days

Placebo

Placebo orally. 1 tablet of Placebo 2 times a day during 14 full days of treatment period

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Participants will receive Placebo 2 times a day during 14 full days

Interventions

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XC221

Participants will receive XC221 100 mg 2 times a day during 14 full days

Intervention Type DRUG

Placebo

Participants will receive Placebo 2 times a day during 14 full days

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Signed Informed Consent Form.
2. Patients of both sexes aged 18 to 75 years inclusive.
3. Diagnosed COVID-19 based on positive laboratory tests confirming the SARS-CoV-2 presence, performed no earlier than 3 days before screening. It is allowed to determine the SARS-CoV-2 by the PCR or by another method according to the MoH Temporary Guidelines.
4. Patients having a total score ≥ 5 according to the COVID-19 Major Symptom Rating Scale.
5. Patients with mild COVID-19, as defined in The MoH Temporary Guidelines. Presence of at least two criteria: SpO2 ≥ 95% (required criterion), 37.5°С ≤ t ˂ 38°С, or respiratory rate (RR) ≤ 22 / min. Absence of moderate/severe progression criteria.
6. Disease duration is no more than 3 full days since the onset of one or more of symptoms below before the first dose of the drug administration:

* body temperature increase;
* dry cough or cough with little phlegm;
* dyspnoea;
* myalgia;
* fatigue;
* feeling of congestion in the chest;
* reduced sense of smell and / or taste.
7. For women only: negative pregnancy test result. Pregnancy testing is not required for women of not childbearing potential (WONCBP): women who are in menopause (defined as an absence of menstruation for at least 2 years or more), or women who undergone surgical sterilization (hysterectomy, bilateral oophorectomy, tubal ligation), or women with a clinical diagnosis of "infertility". The presence of surgical sterilization and infertility should be confirmed by patient's claim or by relevant document confirming this condition.
8. Consent to use reliable method of contraception throughout the study period.
9. Patients who are able to understand and comply with treatment and procedures during the study.

Exclusion Criteria

1. Known or suspected hypersensitivity to the active substance or to excipients of the drug XC221 or placebo
2. Known or suspected hypersensitivity to standard therapy drugs specified in The MoH Temporary Guidelines.
3. Body temperature ˂37.5°С.
4. Lactase deficiency, lactose intolerance, glucose-galactose malabsorption.
5. Presence or suspicion of oncological diseases by the day of criteria assessment or in medical history (within the last 2 years).
6. Presence of autoimmune diseases by the day of criteria assessment or in medical history.
7. Pregnancy.
8. Lactation period.
9. Presence of serious lung diseases, including, but not limited to the following diseases: moderate and severe bronchial asthma, severe and extremely severe COPD, interstitial lung disease, pulmonary hypertension, pulmonary fibrosis, surgical interventions on the lungs, tuberculosis (including suspicion of tuberculosis based on the results of CT examination at screening).
10. Patients with type 1 diabetes mellitus and / or decompensated type 2 diabetes mellitus.
11. Heart failure, NYHA functional class III - IV.
12. Chronic liver failure stage II (decompensated) and higher.
13. The need of replacement renal therapy at enrollment.
14. Organ transplantation in medical history.
15. Medical history of epilepsy or the need for anticonvulsant therapy.
16. Major depressive disorder, anxiety, other mental disorders requiring medical correction.
17. Acute cerebrovascular accident, stroke or transient ischemic attack within 90 days before screening.
18. Use of any antiviral and / or immunomodulatory drugs after the manifestation of COVID-19.
19. Any immunosuppressive therapy (including tocilizumab / sarilumab) within 90 days prior to randomization, or the need of immunosuppressive therapy at the time of randomization.
20. Use of anti-COVID-19 plasma within 14 days prior to the screening visit.
21. Use of systemic glucocorticosteroids within 90 days prior to randomization, or the need of systemic glucocorticosteroids at the time of randomization.
22. Use of vaccines against viral infections within 90 days prior to randomization.
23. Patients receiving other experimental drugs, drugs not approved in the Russian Federation, or participating in other clinical trials within 30 days before screening.
24. Patients abusing alcohol or psychotropic drugs and other drugs by the day of criteria assessment or during the last year.
25. Patients with other serious, unstable, or clinically significant medical or psychological conditions that, in the opinion of the investigator, may preclude the patient's participation in the study.

Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No