Enarodustat Tablets at Different Initial Doses for Anemia in Non-dialysis CKD Patients

Official title

A Prospective, Single-arm, Open-label Study to Evaluate Different Initial Doses of Enarodustat Tablets for the Treatment of Anemia in Patients With Non-dialysis Chronic Kidney Disease

Overview

To evaluate the rationality of different initial doses of enarodustat for the treatment of anemia in ND-CKD patients

Detailed description

The eligible subjects screened will be stratified by treatment history and randomized to the 2, 3, 4 mg dose groups in a 1:1:1 ratio. After receiving the initial doses of 2, 3, 4 mg/day for 4 weeks, the subjects will enter a 12-week maintenance treatment period with a total of 7 scheduled visits.

Interventions

• Drug Enarodustat 2mg
  initial phase：2mg QD for 4 weeks subsequent phase：1mg、2mg、4mg、6mg、8mg QD，adjust the dose based on hemoglobin concentration level every 4 weeks
• Drug Enarodustat 3mg
  initial phase：3mg QD for 4 weeks subsequent phase：1mg、2mg、4mg、6mg、8mg QD，adjust the dose based on hemoglobin concentration level every 4 weeks
• Drug Enarodustat 4mg
  initial phase：4mg QD for 4 weeks subsequent phase：1mg、2mg、4mg、6mg、8mg QD，adjust the dose based on hemoglobin concentration level every 4 weeks

Primary outcome measures

• Mean Hb level at Week 16 of treatment [Time frame: week 16]

Secondary outcome measures (6)

• Cumulative proportion of subjects with Hb levels of ≥100 g/L and ≤120 g/L at each visit [Time frame: week 0,2,4,8,12,16]
• Cumulative proportion of subjects with Hb levels of ≥110 g/L and <130 g/L at each visit [Time frame: week 0,2,4,8,12,16]
• ESA-treated group: cumulative proportion of subjects with Hb levels ±10 g/L from baseline at Weeks 12-16 of treatment; [Time frame: week12- 16]
• Hb levels at each visit [Time frame: week 0,2,4,8,12,16]
• Change in Hb level from baseline at each visit [Time frame: week 0,2,4,8,12,16]
• Dosage of administration of the investigational drug throughout the treatment period [Time frame: 16 weeks]

Eligibility criteria

Inclusion criteria

• Patients who meet all the following criteria can be enrolled in this study:

• Male or female patients aged 18-75 years (inclusive);
• Body weight: 45-100 kg (inclusive);
• Stage 3-5 non-dialysis CKD complicated with renal anemia during the screening period, with an eGFR of 10-60 mL/min/1.73 m2 (exclusive) (calculated by CKD-EPI equation);
• Criteria for Hb levels at screening and baseline

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• ESA-naïve population: Patients who do not receive ESA treatment in the past 12 weeks, with the Hb level greater than or equal to 70 g/L and less than 100 g/L;
• ESA-treated population: Patients who have received ESA treatment for at least 8 weeks, with the Hb level greater than or equal to 100 g/L and less than or equal to 120 g/L; 5.Female patients shall take contraceptive measures during the study; Patients who voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

• Patients who meet any one of the following criteria shall be excluded from the study:

• Patients with SF ≤100 μg/L and TSAT ≤20% at screening;
• Patients who are expected to start renal replacement therapy in the next 6 months as judged by the investigator;
• Patients with systemic hematologic disorders (e.g., myelodysplastic syndrome and aplastic anemia, etc.) or non-CKD-related anemia (hemolytic anemia, hemorrhagic anemia, cancer related anemia, etc.);
• Patients with a 1.5-fold increase in serum creatinine during the screening period;
• Patients who have received hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHI) within 8 weeks before screening;
• Patients with polycystic kidney disease;
• Patients with poorly controlled hypertension (systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg at the screening visit);
• Patients with congestive cardiac failure (New York Heart Association \[NYHA\] Class III or above) or unstable angina;
• Patients who have experienced myocardial infarction, transient ischemic attack, cerebral infarction (except asymptomatic cerebral infarction) or venous thromboembolism (pulmonary embolism or deep vein thrombosis) from 24 weeks before screening to the first dose of the investigational drug;
• Patients with severe hepatobiliary disorders (e.g., AST or ALT >2.5 × upper limit of normal (ULN) at the screening visit, patients with hepatic cirrhosis or total bilirubin ≥1.5 × ULN at the screening visit);
• Patients who have received red blood cell transfusion from 12 weeks before screening to the first dose of the investigational drug;
• Patients who have received growth hormone, thyroid hormone, testosterone enanthate or methandienone from 12 weeks before screening to the first dose of the investigational drug;
• Patients who will undergo elective ophthalmic surgery in the next 6 months;
• Patients with severe hyperparathyroidism (e.g., iPTH ≥500 pg/mL at the screening visit);
• Patients with severe infections (e.g., active pulmonary tuberculosis and fungal infection, etc.);
• Patients suspected of having other non-infectious chronic inflammatory diseases (e.g., systemic lupus erythematosus, rheumatoid arthritis and coeliac disease, etc.);
• Patients with a positive result for HIV, HCV or Treponema pallidum antibody, or with a positive result for HBsAg and HBV DNA ≥1,000 U/mL;
• Patients with a history of malignant tumors (including hematological malignancies) in the past 5 years;
• Patients with a history of severe drug allergy (e.g., anaphylactic shock) or hypersensitivity to other HIF-PHIs;
• Patients with a history of drug or alcohol abuse in the past two years;
• Patients who have received other investigational drugs (or study drugs) or received investigational medical devices (or study devices) from 12 weeks before the screening visit to the first dose of the investigational drug, or are participating in other interventional clinical studies (medical behaviors beyond routine diagnosis and treatment, implemented for study purposes) and receiving treatment;
• Patients who are pregnant, lactating or have the possibility of pregnancy (based on the results of the pregnancy test at the screening visit, the investigator cannot rule out the possibility of pregnancy);
• Patients with any medical conditions that, in the investigator's judgment, may pose a safety risk, may confound efficacy or safety evaluation, or may interfere with their participation in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Chinese PLA General Hosptial — Beijing

Identifiers

NCT: NCT07079579 · SAL0951A401

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗