CTRI/2021/04/032791已完成3 期
A randomized, double-blind, placebo-controlled, Phase III trial to determine the efficacy and safety of inhaled SNG001 for the treatment of patients hospitalized due to moderate COVID-19 - SPRINTER
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 72
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1) Admitted to hospital due to the severity of their COVID-19
- •2) Positive virus test for SARS-CoV-2 using a validated molecular assay or antigen assay. Patients who had a positive virus test for SARS-CoV-2 prior to hospitalisation will be randomised no later than 48 hours after hospital admission. If the virus test is performed more than 96 hours prior to hospitalisation, the test will have to be repeated in the hospital prior to randomisation. Only patients whose repeated virus test is positive will be randomised, no later than 48 hours after confirmation of SARS-CoV-2 infection. Patients who had their first positive virus test for SARS-CoV-2 after hospitalisation will be randomised no later than 48 hours after confirmation of SARS-CoV-2 infection
- •3) Require oxygen therapy via nasal prongs or mask (WHO OSCI score of 4)
- •4) Provided informed consent
- •5) Female patients must be greater than or equals to 1 year post-menopausal, surgically sterile, or using a protocol defined highly effective method of contraception
- •6) Women of child bearing potential should have been stable on their chosen method of birth control for a minimum of 3 months before entering the trial and should continue with birth control for 1 month after the last dose of inhaled interferon-beta (IFN-beta 1a)/matching placebo. In addition to the highly effective method of contraception (except for the practice of total sexual abstinence), a condom (in United Kingdom with spermicides) should be used by the male partner for sexual intercourse from randomisation (Visit 2) and for 1 month after the last dose of inhaled IFN-beta1a/matching placebo to prevent pregnancy
- •7) Women not of childbearing potential are defined as women who are either permanently sterilised (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy), or who are postmenopausal. Women will be considered post-menopausal if they have been amenorrhoeic for 12 months prior to the planned date of randomisation without an alternative medical cause. The following age specific requirements apply: women less than 50 years old will be considered post-menopausal if they have been amenorrhoeic for 12 months or more following cessation of exogenous hormonal treatment and if follicle stimulating hormone (FSH) levels are in the postmenopausal range; women greater than or equals to 50 years old will be considered post-menopausal if they have been amenorrhoeic for 12 months or more following cessation of all exogenous hormonal treatment. If, in the setting of the pandemic, the use of an acceptable birth control method is not possible, the decision to enroll a woman of childbearing potential should be based on the benefit-risk for the patient, which should be discussed with the patient at the time of the informed consent
排除标准
- •1) Evidence of ongoing SARS-CoV-2 infection for more than 3 weeks, confirmed by a validated molecular assay or validated antigen assay
- •2) Non-invasive ventilation (CPAP/BiPAP) or high-flow nasal oxygen - therapy (WHO OSCI score of 5)
- •3) Endotracheal intubation and invasive mechanical ventilation (HO OSCI score of ââ?°Â¥6)) or admission to intensive care
- •4) Previous SARS-CoV-2 infection confirmed by a validated molecular assay or validated antigen assay
- •5) Any condition, including findings in the patients medical history or in the pre-randomisation study assessments that in the opinion of the Investigator, constitute a risk or a contraindication for the participation of the patient into the study or that could interfere with the study objectives, conduct or evaluation
- •6) Participation in previous clinical trials of SNG001
- •7) Current or previous participation in another clinical trial where the patient has received a dose of an Investigational Medicinal Product containing small molecules within 30 days or 5 half-lives (whichever is longer) prior to entry into this study or containing biologicals within 3 months prior to entry into this study
- •8) Inability to use a nebuliser with a mouthpiece
- •9) Inability to comply with the requirements for storage conditions of study medication in the home setting
- •10) History of hypersensitivity to natural or recombinant IFN-Ã?² or to any of the excipients in the drug preparation
- •11) Females who are breast-feeding, lactating, pregnant or intending to become pregnant
研究者
相似试验
进行中（未招募）
不适用
A randomized, double-blind, placebo-controlled, Phase III trial of 2 regimens of telaprevir (with and without delayed start) combined with pegylated interferon alfa-2a (Pegasys®) and ribavirin (Copegus®) in subjects with chronic genotype 1 hepatitis C infection who failed prior pegylated interferon plus ribavirin treatment. - REALIZEEUCTR2008-000533-22-ATTibotec BVBA650
进行中（未招募）
1 期
Comparison of a single RTX-GRT7039 and placebo intra-articular injection for pain associated with osteoarthritis of the knee.EUCTR2021-005020-38-ESGrünenthal GmbH450
招募中
1 期
A randomized, double-blind, placebo-controlled, Phase 2b trial of GH001 in patients with treatment resistant depressioTreatment-resistant depression (TRD)MedDRA version: 21.1Level: PTClassification code 10057840Term: Major depressionSystem Organ Class: 10037175 - Psychiatric disordersEUCTR2022-000574-26-IEGH Research Ireland Limited80
招募中
3 期
Comparison of RTX-GRT7039 and placebo injections for pain associated with osteoarthritis of the knee.Moderate to severe pain associated with osteoarthritis of the kneeJPRN-jRCT2031220354ange Bernd, MD, MSc, Medical Lead90
招募中
3 期
A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of intra-articular injections of RTX-GRT7039 in adult subjects with pain associated with osteoarthritis of the kneeNL-OMON51845Grunenthal15