CTRI/2021/03/032446招募中2 期
An Open-label, Randomized, Three Arm, comparative, standard control Clinical Study to evaluate the safety and efficacy of HAVR-122008 in the Treatment of uncomplicated respiratory viral infection.
试验速览
- 阶段
- 2 期
- 状态
- 招募中
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.Subjects of either gender aged more than >18 â?? <65 years.
- •2.Subjects suffering from acute respiratory illness with one or more signs and symptoms consistent with a viral infection (eg. fever, headache, nasal discharge, fatigue, sore throat, sneezing, cough, sleep disturbance, muscle or body aches etc)
- •3.Onset of symptoms within 3 days from the anticipated time of randomization. Onset of symptoms is defined as the time the subject becomes aware of the first sign and/or symptom consistent with a viral infection.
- •4.Subject must be medically stable on the basis of physical examination, medical history and vital signs performed at screening.
- •5.Ability to understand and willing to give a written informed consent prior to any study-related procedures and ready to follow and in agreement to visits as per the study assessment visits
- •6.Women of child-bearing potential and men with partners of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 15 days following completion of therapy.
排除标准
- •1.Subjects with opportunistic infections / severe infections requiring of Anti-viral / Anti-Bacterial medication at screening.
- •2. Hospitalized subjects or subjects expected to be hospitalized during the study duration.
- •3.Individuals with acute respiratory distress.
- •4.Subjects suffering from severe and uncontrolled metabolic, endocrinal, cardiac/renal/liver diseases
- •5.Subjects with known hypersensitivity to any of the test materials or related compounds.
- •6. Subjects who had major surgery within the 28 days prior to randomization or have planned major surgery through the course of the study
- •7. Subject with a history of known or suspected chronic or acute hepatitis B or C infection
- •8.Women who are pregnant or breastfeeding
- •9.Pre-existing systemic disease necessitating long-term medications.
- •10.Genetic and endocrinal disorders.
研究者
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