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NCT07494409RecruitingPhase 3

A Study of AND017 to Evaluate Efficacy and Safety in Dialysis-Dependent Chronic Kidney Disease (DD-CKD) Patients With Anemia

A Phase 3, Multi-center, Randomized, Open-Label, Active-Controlled, Efficacy and Safety Study of AND017 to Treat Anemia in Dialysis-Dependent Chronic Kidney Disease (DD-CKD) Patients With Anemia

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

This is a phase III, randomized, open-label, active-controlled study to evaluate the safety and efficacy of AND017 in anemic patients with End-Stage-Kidney-Disease (ESKD)

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
300 (estimated)
First submitted
20 Mar 2026
Start date
Oct 2025
Primary completion date
Oct 2026
Lead sponsor
Kind Pharmaceuticals LLC
NCT number
NCT07494409

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 300
  • From Oct 2025 to the primary completion date, Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent retinal neovascular lesions requiring treatment
  • Chronic inflammatory disease other than glomerulonephritis that could impact erythropoiesis or concurrent autoimmune disease with inflammatory symptoms
  • History of gastric/intestinal resection considered to affect the absorption of drugs in the gastrointestinal tract or concurrent symptomatic gastroparesis despite being on treatment
  • Concurrent congestive heart failure (New York Heart Association \[NYHA\] Class III or higher)
  • History of stroke, transient ischemic attack (TIA), myocardial infarction, thromboembolic event (deep vein thrombosis, DVT), pulmonary embolism, or lung infarction within 24 weeks before the screening assessment
  • Any prior functioning organ transplant or a scheduled organ transplantation, or anephric

Other illness

  • Uncontrolled hypertension, defined as patients with hypertension having more than one of three systolic blood pressure \>180 mmHg, or diastolic blood pressure \>110 mmHg during the screening assessment
  • Participants with a history of significant liver disease or active liver disease
  • History of a seizure disorder or any occurrence of seizures in the past

Lab values

  • Serum albumin (ALB) \< 2.5 g/dL at screening test
  • Prior ESA/hypoxia-inducible factor-prolyl hydroxylase inhibitor (HIF-PHI) treatment caused total bilirubin \>1.5xULN, or AST/ALT/ ALP\>3xULN, or serious liver disease (acute or active chronic hepatitis, cirrhosis, etc.)

Who the study is looking for

  • Receiving stable hemodialysis (including combination methods such as hemodiafiltration or hemofiltration), peritoneal dialysis for ESKD for a minimum of 16 weeks prior to randomization and determined by the Investigator to be compliant with dialysis treatment prescription.
  • Patient must have been on IV or SC of an approved ESA under the prescription for at least 6 weeks
  • The mean of two hemoglobin values during screening must be 9.0-12.0 g/dL.
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT)\<3× upper limit of normal (ULN)
  • Transferrin saturation ≥20% or ferritin ≥100 ng/mL at screening test
  • Serum folate and vitamin B12 ≥ lower limit of normal (LLN) at screening test

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan Univeristy Zhongshan Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.