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Efficacy and safety study of an Epoetin alfa in Thai patients under CAPD.

An open-label prospective study to evaluate the efficacy and safety of a recombinant human Erythropoietin (Hema-Plus) for the management of anemia in patients on peritoneal dialysis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20140128002
Enrollment
30
Registered
2014-01-28
Start date
2014-02-25
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal anemia renal anemia anemia in chronic kidney disease

Interventions

Epoetin alfa 4000 IU SC initially once a week&#44
dosage adjustment can be performed during the treatment period upon investigator discretion
Experimental Biological/Vaccine
Epoetin alfa

Sponsors

Apexcela, Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who have consented to participate in the study in writing 2. Patients with chronic renal disease whose GFR is less than 15 ml/min/1.73 m2 and are identified to start peritoneal dialysis 3. Age between 18-70 years on the day of consent 4. Hemoglobin 100 ng/ml and serum transferrin saturation (TSAT) > 20%

Exclusion criteria

Exclusion criteria: Main exclusion criteria 1. Patients who have previously used Epoetin 2. Patients who are pregnant or breastfeeding or women of childbearing potential who are not willing to use an effective method of birth control 3. Participation in any drug trial in which the patient received an investigational drug within 3 months prior to screening visit. 4. Patients who have the underlying conditions - had blood transfusion within 8 weeks prior to screening visit - Poorly controlled hypertension with diastolic blood pressure greater than 110 mmHg at screening visit. - History of seizure disorder - Previous diagnosis with malignant tumor or patients who had residual tumor after anti-cancer therapy elicited by medical history - Patients with signs and symptoms or laboratory assessment associated with EPO-resistant bone marrow disease such as aplastic anemia, myelodysplastic syndrome, myelofibrosis, myelopthistic anemia or Pure Red Cell Aplasia (PRCA) - Known hypersensitivity to the mammalian cell-derived product or human albumin products 5. Patients who are using concomitant androgens or immunosuppressive therapy 6. Patients who have Secondary hyperparathyroidism as evaluated by serum parathyroid hormone (PTH) level greater than 800 pg/ml at screening

Design outcomes

Primary

MeasureTime frame
Mean Hb level week 12 Hb level

Secondary

MeasureTime frame
Safety week 12 Adverse events

Countries

Thaialnd

Contacts

Public ContactNarumon Werayingyong

Industry

narumonw@siambioscience.com026139939

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026