Study on Single and Multiple Atomization Inhalation of HRS-9821 Suspension for Inhalation in Healthy Subjects and COPD Patients

Hengrui Medicine

Status and phase: Active, not recruiting; Phase 1

Conditions: Chronic Obstructive Pulmonary Disease

Treatments: Drug: HRS-9821

Study type: Interventional

Funder types: Industry

Identifiers

NCT05622864

HRS-9821-I-101

Details and patient eligibility

About

The increased safety and tolerance of single and multiple atomized inhalation of HRS-9821 suspension for inhalation doses in healthy subjects and COPD patients.

Enrollment: 106 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Sign an informed consent forms；

2. Aged 18-75 (both ends, subject to the signing of the informed consent form);

3. Weight ≥45 kg，BMI 18-33 kg/m2 (include 33 kg/m2);

4. During the screening period, the vital signs of healthy subjects are normal:

   • Shrinkage 90-140 mmHg,
   • diastolic pressure 50-90 mmHg,
   • Heart rate 40-100 times/min;

5. During the screening period, the lung function of healthy subjects is normal, that is, the predicted value of FEV1≥80% and the predicted value of FEV1/FVC≥92%;

6. During screening, the 12-lead ECG is normal or abnormal but has no clinical significance.

7. Follow the contraceptive requirements within 14 weeks from the beginning of the consent to the last dose, and do not donate sperm during the consent period;

8. During the study, all research regulations and procedures can be followed, and the atomization devices used by the research institute can be used correctly;

9. Healthy subjects: non-smoking or quitting smoking ≥ 12 months, the previous smoking history < 5 packs of years.

Exclusion criteria

1. Healthy subjects: in the past 12 weeks, antibiotics have been used for upper and lower respiratory tract infections, or have a history of respiratory infections within the past 4 weeks;
2. Abnormal laboratory or physical examination results of clinical significance
3. The average value of QTcF for 3 times at screening is ≥450ms;
4. In the past four weeks, there have been blood donations or large blood loss (more than 400 milliliters), or those who intentionally donate blood during the study
5. Accept experimental drugs or use experimental medical devices within 1 months or less than 5 times the half-life of the drug, whichever is longer;
6. In the past, there were difficulties in collecting blood or could not withstand intravenous puncture, such as needle halo and blood halo
7. Any organ system has a history of malignant tumors;
8. Known to be allergic to any accessories in the research drug or formulation;
9. Previously known infection of human immunodeficiency virus (HIV), hepatitis B virus (HBV) liver or hepatitis C virus (HCV); or randomized pre-HIV (according to the test center SOP), treponema pallidum antibody (TPPA), HBV surface antigen or HCV antibody positive;
10. There is a history of smoking and alcoholism in the 3 months before screening: smoking (more than 5 cigarettes or equivalent tobacco per day); alcoholism (more than 14 units of alcohol per week: 1 unit = 360mL of beer, or 25mL of spirits with a concentration of 40% or more, or 1 glass of wine, 180mL);
11. In the past five years, there has been a history of drug abuse and drug dependence.
12. Before randomization, positive for alcohol or drug abuse or nicotine in urine.
13. During the study, there is a surgical plan or may interfere with the treatment plan carried out by the study;
14. Inability or unwillingness to fully comply with the research program;
15. Mentally or legally incapacitated;
16. The researchers believe that there are any other reasons why the subjects are unfit to participate in the study;
17. Prescription was used within 14 days before the first administration or within 48 hours before the first administration;
18. Drugs that have used strong/intermediate inhibitors or induce liver drug metabolic enzyme CYP3A4 14 days before the first administration or ingest grapefruit or related products within 7 days before the first administration;
19. During the study, it was expected to use drugs that had an effect on P-gp or breast cancer drug-resistant protein (BCRP).

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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106 participants in 2 patient groups

PartA

Experimental group

Treatment:

Drug: HRS-9821

Drug: HRS-9821

PartB

Experimental group

Treatment:

Drug: HRS-9821

Drug: HRS-9821