A Phase 1 Clinical Trial of NTQ5082 in Healthy Volunteers
Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-45
SponsorNanjing Chia-tai Tianqing Pharmaceutical
About this trial
NTQ5082 capsule is a small molecule CFB factor inhibitor. The study is a randomized, double-blind, placebo-controlled, dose escalation phase 1 clinical trial to evaluate the safety, tolerability and PK/PD characteristics of NTQ5082 capsules orally administered in healthy subjects in single and multiple doses.
Eligibility criteria
Qualifiers
Healthy male or female, ≥18 years and ≤45 years in age.
19.0 kg/m2≤BMI≤26.0 kg/m2, and male weight must be ≥50 kg, female weight must be ≥45 kg;
Those who sign an informed consent form before the experiment and fully understand the content, process, and possible adverse reactions of the experiment;
The subjects are able to communicate well with the researchers and understand and comply with the requirements of this study.
Disqualifiers
Participants who have participated in any other drug clinical trials and used the investigational drug within 3 months prior to the trial;
Individuals who have chronic or active gastrointestinal diseases such as esophageal disease, gastritis, gastric ulcer, gastroesophageal reflux, enteritis, active gastrointestinal bleeding, or gastrointestinal surgery within the past three years, and who are still clinically significant according to researchers;
Individuals with clear diseases of the central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, hematological system, metabolic disorders, etc. that require medical intervention or other diseases that are not suitable for clinical trials (such as a history of mental illness);
Known or suspected history of immunodeficiency (such as frequent recurrent infections), genetic or acquired complement deficiency;
Trial design
Treatments tested in this trial
- NTQ5082
- Placebo
Treatment groups
82 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov