A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Food Effects of Single and Multiple Administration of F230 Tablets in Healthy Adult Volunteers

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

F230 is a new Class 1 chemical drug jointly developed by Beijing Contini Pharmaceutical Co., Ltd. for the treatment of pulmonary hypertension (Notification number: 2024LP01242, 2024LP01243). The in vitro activity and in vivo toxicology tests of F230, the lead compound for the treatment of PAH developed by Beijing Contini Pharmaceutical Co., LTD., showed that F230 had the same in vitro activity as the endothelin antagonist on the market. The pharmacodynamics of F230 in rats with nephrogenic hypertension induced by Sunitinib showed that F230 could reduce proteinuria and improve renal index.It is expected to bring higher treatment and survival benefits to the corresponding patients. According to the spirit of NMPA new drug approval, on the basis of the completion of preclinical studies of this drug, the safety, tolerability and pharmacokinetic characteristics of single administration and multiple administration of this drug in healthy volunteers should be investigated first, and the influence of food on the pharmacokinetic characteristics of F230 in humans should be investigated, so as to recommend a safe and effective administration regimen for phase II clinical trials.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: t
View:

‣ Volunteers must meet all of the following criteria to be selected:

⁃ Healthy volunteers, half male and half female, should be replaced by volunteers of the same sex;

⁃ Age: 18 \

• 45 years old;

⁃ Weight: male ≥50kg, female ≥45kg, 19≤BMI≤26 (BMI= weight (kg)/height 2 (m2));

⁃ Pass the comprehensive health examination: vital signs, physical examination, blood urine routine, blood pregnancy, blood glucose, blood lipid, blood electrolyte, hepatitis B surface antigen, liver and kidney function, hepatitis C, HIV and syphilis antibody test, 12-lead electrocardiogram, nicotine, urine drug screening, alcohol breath test, abdominal B-ultrasound, chest X-ray examination, etc., no abnormalities or abnormalities have no clinical significance;

⁃ Before participating in the study, have a detailed understanding of the nature, significance, possible benefits, possible inconveniences and potential dangers of the trial, and voluntarily participate in this clinical trial, can communicate well with the investigators, comply with the requirements of the entire study, and have the ability to understand and sign the written informed consent.

Locations
Other Locations
China
Union Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology
RECRUITING
Hubei
Contact Information
Primary
shaojun Shi, Dr
sjshicn@163.com
027-85726085
Backup
Rui Zhang, Dr
392519821@qq.com
155272727759
Time Frame
Start Date: 2025-05-15
Estimated Completion Date: 2026-07-01
Participants
Target number of participants: 136
Treatments
Experimental: SAD single dose group
A total of 6 dose groups A1-A6: F230 are initially expected to be developed (A1-A6 test groups were administered 3mg, 6mg, 12mg, 20mg, 30mg, 40mg, respectively). The specific incremental dose can be adjusted according to the test situation. The A1 dose group included 8 volunteers (stratified by sex, F230 tablets: placebo =3:1), and the A2 to A6 dose group included 14 volunteers (stratified by sex, F230 tablets: Placebo =6:1), F230 tablets or placebo were taken orally on an empty stomach on the day of administration. From the night before the start of the trial to the end of the trial evaluation period (A1:D-1 \~ D3/A2-A6:D-1 \~ D2), the volunteers were kept in the phase I research room. During the study period, safety assessment and PK biological sample collection were conducted according to the protocol. The volunteers completed a safety check on day 3(A1)or day2(A2-A6).
Experimental: MAD multiple dose group
It is preliminarily expected to carry out 3 dose groups, preset 6mg, 12mg, 20mg, the frequency of administration will be determined according to the results of a single administration test, continuous administration for 7 days. 14 volunteers were included in each group (stratified by sex, F230 tablets: placebo = 6:1), and a total of 42 volunteers were planned to be included. All volunteers were in the research center from the day before administration (D-1) to 24h after the last administration (D8). During the study period, safety assessment and PK biological sample collection were conducted according to the protocol. On the 8th day of the study (D8, 24h after the last administration), the procedures prescribed in the protocol and related safety checks were completed, and they could leave the research center after comprehensive evaluation by the researchers. The volunteers then returned to the study center on day 9 (D9,48h after the last dose) or for safety follow-up.
Experimental: Research on the effects of food on drugs
It is planned to include 16 volunteers. A stratified block randomization method was adopted, with gender as the stratification factor. Volunteers were randomly assigned to two drug administration sequence groups (K-C group and C-K group), with 8 cases in each group. That is, 8 volunteers were administered on an empty stomach in the first cycle, and the other 8 volunteers were administered within half an hour after consuming a high-fat meal in the first cycle and eluted on the second day (D2). After a total of 3 days (72 hours) of elution, the volunteers received the second cycle of administration on the 6th day (D6). Volunteers who received the drug on an empty stomach in the first cycle were given the drug within half an hour after a high-fat meal. Volunteers who received the drug after a high-fat meal in the first cycle were given the drug on an empty stomach. Complete the procedures stipulated in the plan and related safety checks on the 7th day of the study.
Related Therapeutic Areas
Sponsors
Leads: Beijing Continent Pharmaceutical Co, Ltd.

This content was sourced from clinicaltrials.gov