HEC53856 Phase Ib Study in Patients With Non-dialysis Renal Anemia

NCT ID: NCT04925661

Last Updated: 2025-05-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-11-04
• Study Completion Date: 2023-08-29

Brief Summary

To evaluate the safety, tolerability , pharmacokinetics and Preliminary Efficacy of HEC53856 Capsules in Patients With Non-dialysis Renal Anemia.

Detailed Description

This is a MultiCenter, Randomized, Blinded, Active Drug and Placebo-controlled, Dose-escalated Phase Ib Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of HEC53856 Capsules in Patients With Non-dialysis Renal Anemia. Each part participants will be randomly administrated for HEC53856 or placebo or roxadustat.

The study consisted of three study periods as follows:

Screening period: up to 2 weeks； Treatment period: 8 weeks； Post-Treatment Follow-Up period: 4 weeks.

Conditions

Chronic Kidney Diseases; Renal Anemia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

HEC53856

Drug: HEC53856 TIW dosing, capsule There will be a total of 3 dose cohorts: 100mg, 150mg, 200 mg

Group Type: EXPERIMENTAL

HEC53856

Intervention Type: DRUG

Either dose of HEC53856 will be administered after fasting .

Roxadustat

Drug: roxadustat TIW dosing There will be only one cohort: 70mg

Group Type: ACTIVE_COMPARATOR

Roxadustat

Intervention Type: DRUG

Roxadustat will be administered after fasting .

Placebo

Drug: placebo TIW dosing, capsule There will be a total of 3 dose cohorts: 100mg, 150mg, 200 mg

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Either dose of placebo will be administered after fasting .

Interventions

HEC53856

Either dose of HEC53856 will be administered after fasting .

Intervention Type: DRUG

Roxadustat

Roxadustat will be administered after fasting .

Intervention Type: DRUG

Placebo

Either dose of placebo will be administered after fasting .

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients who agree to participate in this clinical trial and sign an informed consent form;

2. Age 18~65 years old; Weight 40~90Kg, including critical value;

3. Glomerular filtration rate (eGFR) calculated by CKD-EPI formula 15mL/min/1.73 m^2 < or = eGFR < 60 mL/min/1.73 m^2 diagnosed chronic kidney disease patients who have not received dialysis;

4. The hemoglobin values obtained during the last two screening periods at least 6 days apart must be > or = 8.0 g/dL and <10 g/dL.

Exclusion Criteria

1. Existence of diseases or conditions other than nephropathy that may cause anemia, including but not limited to 1) blood system diseases, such as thalassemia, aplastic anemia, hemolytic anemia, multiple myeloma, myelodysplastic syndrome, etc.; 2) may affect red blood cells The resulting autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, etc.; 3) Bleeding diseases, such as gastrointestinal bleeding, obstetrics and gynecology bleeding diseases, etc.; 4) Elective surgery expected during the study period;

2. Drugs used to treat anemia within 8 weeks before the first administration, including but not limited to erythropoiesis stimulators (ESAs) and their derivatives, hypoxia inducible factor prolyl hydroxylase inhibitors (HIF-PHI), androgens And anabolic hormone drugs, intravenous iron, Chinese patent medicine, Chinese herbal medicine, etc. (Can accept patients who have used a fixed dose of oral iron within 4 weeks before screening, and continue to take it during the screening period and the first 4 weeks after starting to take the test drug The fixed dose remains unchanged.);

3. Those who have received blood transfusion within 3 months before the first administration;

4. Folic acid <6.8nmol/L (3ng/ml) and (or) VitB12<74pmol/L (100ng/ml) during the screening period;

5. Clinically significant chronic liver and gallbladder disease, or obvious abnormal liver function: ALT>3×ULN and/or AST>3×ULN, or total bilirubin>1.5×ULN;

6. Serum albumin <3 g/dL;

7. The mean systolic blood pressure > or = 160 mmHg and/or the diastolic blood pressure > or = 100 mmHg of the two blood pressure measurements at least one hour apart during the screening period;

8. Suffering from uncontrollable or symptomatic secondary hyperparathyroidism, plasma iPTH > 500pg/ml;

9. A history of acute or chronic pancreatitis, or acute or chronic pancreatitis at the time of screening, or blood amylase > or = 3×ULN;

10. History of malignant tumors within 5 years (except for cured skin basal cell carcinoma and cervical carcinoma in situ), or current assessment of potential malignant tumors;

11. Patients with acute coronary syndrome, stroke ( except for lacunar infarction )or thromboembolic diseases (such as deep vein thrombosis or pulmonary embolism) occurred in the 6 months before screening;

12. New York Society of Cardiology, grade III or IV congestive heart failure, or severe arrhythmia, including but not limited to atrial fibrillation, III degree atrioventricular block, etc.;

13. AIDS antibody, Treponema pallidum antibody, hepatitis B surface antigen or hepatitis C antibody positive for any of them;

14. People with a history of severe allergic disease or drug allergy, or those who are allergic to experimental drugs or their excipients;

15. Patients with clinically severe infections who are receiving systemic antibiotic treatment;

16. Those who have started dialysis or plan to start dialysis treatment within 6 months;

17. Anyone who has participated in or plans to participate in organ transplantation within 6 months;

18. Patients with hemoglobinosis, polycystic kidney disease, or no kidney;

19. Women during pregnancy or lactation, or fertile men and women who refuse to take effective contraceptive measures voluntarily from the beginning of screening to 4 weeks after the administration of the last trial drug;

20. Participated in other clinical trials within 3 months before screening (Definition of participation: accepted trial drug or instrument);

21. The investigator believes that there are other factors that are not suitable for participating in this trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Nicoya Therapeutics (Shanghai) Co., Ltd.

UNKNOWN

Sponsor Role: collaborator

Sunshine Lake Pharma Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The sixth Affiliated Hospital, Sun Yat-sen University

Guangzhou, , China

Zhejiang Provincal People's Hospital

Hangzhou, , China

The People's Hospital of Guangxi Zhuang Autonmous Region

Nanning, , China

Huashan Hospital

Shanghai, , China

Ruijin Hospital

Shanghai, , China

The First Affiliated Hospital of Xinjiang Medical University

Ürümqi, , China

First Affiliated Hospital of Xi'an Jiaotong University

Xi'an, , China

The First Affiliated Hospital of Xiamen University

Xiamen, , China

Countries

China

Other Identifiers

HEC53856-RAD-102

Identifier Type: -

Identifier Source: org_study_id