Study to Evaluate the Tolerance and Pharmacokinetics of Suramin Sodium

• Status: Unknown status
• Trial end date: 2020-12-19
• Target enrollment: 0
• Participant gender: All

Summary

This is a randomized, double-blind, placebo-controlled, single-dose with three incremental doses, Phase 1 study to evaluate the tolerance and pharmacokinetics of suramin sodium for injection in Chinese healthy adults.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: First Affiliated Hospital of Zhejiang University
• Collaborator: Guangdong Kangda Pharmaceutical Co., Ltd
• Treatments: Suramin

Criteria

Inclusion Criteria:

1. Healthy volunteers who fully understand the purpose, content, benefits and possible adverse reactions of the test and voluntarily sign written informed consent prior to the commencement of any test-related activities.

2. Healthy males or females, aged 18 to 45 years (including 18 and 45 years).

3. Male subjects weighed 50-75 kg (including 50 and 75 kg), female subjects weighed 45-75 kg (including 45 and 75 kg), body mass index (BMI) was 18.0-26.0 kg/m2 (including 18.0 and 26.0 kg/m2), where BMI = body weight (kg)/height2 (m2).

4. Have the ability to communicate with investigator and abide by the management regulations of the hospital and the clinical research.

Exclusion Criteria:

1. Fail in physical examination, vital signs measurement, standard 12-lead electrocardiogram, chest X-ray, laboratory examination [blood routine, urine routine, blood biochemistry, blood coagulation function, infectious diseases, blood pregnancy (only for women of childbearing age), as judged by the investigator to be of clinical significance.

2. With gastrointestinal tract, kidney, liver, nerve, blood, endocrine, tumor, lung, immunity, mental or cardiovascular diseases.

3. Has allergic constitution (allergic to two or more substances), or allergic history, or known allergic to suramin sodium.

4. Cannot tolerate venipuncture and/or have a history of fainting blood or needle.

5. Has massive blood loss (> 400 mL) or had donated blood/blood components within the first six months of screening, or who planned to donate blood/blood components during the study period.

6. Had participated in clinical trials of drugs and took research drugs within three months before screening.

7. Smoke more than five cigarettes a day (including nicotine substitutes) or the same amount of tobacco products in the first three months of screening.

8. Has history of drug abuse within 5 years before screening, or those who had used drugs within 3 months before screening.

9. Has a history of alcoholism or moderate alcoholism in the first two years of screening (moderate alcoholism is defined as drinking more than 3 units per day or 21 units per week; a bottle of 350 mL beer, 120 mL white wine, 150 mL wine or 30 mL spirits is one unit).

10. Pregnant or lactating women, or subjects (or their partners) who have pregnancy plans during the trial and within three months after the end of the study, or who do not agree to use non-drug contraceptive measures during the trial.

11. Positive urine drug screening in screening stage.

12. Alcohol urine positive in screening stage.

13. Nicotine positive in screening stage.

14. With acute diseases in screening period.

15. Had used any prescription, over-the-counter, vitamin products or Chinese herbal medicines within 14 days before enrollment.

16. Female subjects of childbearing age who did not take non-drug contraceptive measures within 14 days before admission.

17. Not suitable for participating into the trial as judged by the investigator.