The Pharmacokinetics (PK), Safety, Tolerability of SR750 in Healthy Volunteers

SIMR Biotech

Status and phase: Completed; Phase 1

Conditions: Healthy

Treatments: Drug: Placebo; Drug: SR750 tablet

Study type: Interventional

Funder types: Industry

Identifiers

NCT05753033

SR750-102

Details and patient eligibility

About

This is a randomized, double-blind, placebo-controlled phase I PK bridging study to evaluate the PK, safety and tolerability of SR750 in healthy subjects.

Enrollment: 56 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Healthy males and females who are 18 to 45 years of age.
2. Based on medical history, physical examination, laboratory examination, chest X-ray, abdominal B-ultrasound, vital signs and ECG, the investigator considered that the results were normal or abnormal but no clinical significance.
3. Bodyweight of male > 50 kg, Bodyweight of female > 45 kg and body mass index (BMI) between 18 and28 kg/m2
4. Male subjects must agree to use contraception methods.
5. Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion criteria

1. Known history of renal dysfunction or creatinine clearance < 90 mL/min (calculated using the Cockcroft-Gault formula) at Screening.

2. Current or chronic history of liver disease or known hepatic or biliary abnormalities.

3. History of regular alcohol consumption within 6 months of screening defined as: an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (~285 mL) of beer, 1 glass (125 mL) of wine or 1 measure (25 mL) of spirits.

4. History of significant drug abuse within one year of screening or use of soft drugs (such as marijuana) within 3 months prior to screening or hard drugs (such as cocaine, methamphetamine, crack) within 1 year prior to screening.

5. History of sensitivity to any of the investigational medicinal products (IMPs), or components thereof or a history of drug or other allergy that, in the opinion of the Investigator or Medical Monitor, contraindicates participation.

6. History of asthma (excluding resolved childhood asthma), severe allergic responses.

7. History of hypercoagulable state or history of thrombosis.

8. A positive Hepatitis B surface antigen, positive Hepatitis C antibody and positive test for human immunodeficiency virus (HIV) antibody.

9. Within 6 months of screening, Smoking more than 4 cigarettes per day (including e-cigarettes).

10. A positive drug/alcohol result at Screening or Day -1.

11. Donation or lost in excess of 500 mL of blood within 56 days of Day 1 or donation of plasma within 14 days of Day 1.

12. The subject has participated in a clinical trial within 3 months of receiving IMP.

    Use of medication other than topical products without significant systemic absorption.

13. Unable to refrain from consumption of Seville oranges, grapefruit or grapefruit juice within 24h prior to the first dose of IMP until the Safety Follow-up visit.

14. Female subjects with positive pregnancy test results.

15. The investigator will determine any conditions in which subjects are not suitable for the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Triple Blind

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56 participants in 2 patient groups, including a placebo group

SR750 tablet

Experimental group

Description:

Ascending single and multiple doses of SR750 orally

Treatment:

Drug: SR750 tablet

Placebo

Placebo Comparator group

Description:

Ascending single and multiple doses of placebo orally

Treatment:

Drug: Placebo