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临床试验/CTRI/2021/03/032446
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.

The Himalaya Drug Company0 个研究点目标入组 0 人开始时间: 待定最近更新:

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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