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A Retrospective Study of the Efficacy and Safety of Hema-Plus (Recombinant Human Erythropoietin Alfa) in Patients with Chronic Kidney Disease who continuously used Hema-Plus at Siriraj Hospital

A Retrospective Study of the Efficacy and Safety of Hema-Plus (Recombinant Human Erythropoietin Alfa) in Patients with Chronic Kidney Disease who continuously used Hema-Plus at Siriraj Hospital

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
TCTR
Registry ID
TCTR20170808001
Enrollment
200
Registered
2017-08-08
Start date
2017-08-15
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

&#45

Interventions

Patients who received Hema&#45
Plus (erythropoietin alfa) for at least 6 months during 1 September 2013 to 31 December 2016.
Treatment

Sponsors

Apexcela Co., Ltd.
Lead Sponsor
Siam Bioscience Co.&#44
Collaborator
Ltd.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Each patient included in the review must meet all of the following criteria to be in this study: 1. Presented with chronic kidney disease 2. History of receiving Hema-Plus for at least 6 months during the study period

Exclusion criteria

Exclusion criteria: 1. Subjects who met inclusion criteria but their medical records are not available for access.

Design outcomes

Primary

MeasureTime frame
Mean hemoglobin values After treating with study drug Hemoglobin value,Adverse events After treating with study drug Adverse events,Proportion of patient achieving target hemoglobin value of 11-12 g/dL After treating with study drug Number of patient who achieved target hemoglobin,Mean difference between base line hemoglobin and follow up hemoglobin Before and after treating with study drug Hemoglobin value

Secondary

MeasureTime frame
NA NA NA

Countries

Thailand

Contacts

Public ContactDuanghathai Tinsulanonda

Siam Bioscience Co., Ltd.

duanghathait@siambioscience.com02 613 9939

Outcome results

None listed

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