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Clinical Trial Details

Trial ID: L1516
Source ID: NCT02522975
Associated Drug: Epiao®
Title: Biosimilar Erythropoietin in Anaemia Treatment (Correction Phase Study)
Acronym: BEAT_001
Status: TERMINATED
Study Results: NO
Results:
Conditions: Renal Anaemia
Interventions: DRUG: EPIAO®|DRUG: EPREX®
Outcome Measures: Primary: Mean absolute change in haemoglobin(Hb), Mean absolute change in haemoglobin(Hb) level from baseline to 24 weeks after treatment with EPIAO®/EPREX® in parallel groups (g/dl),respectively.", 24 weeks | Secondary: Mean absolute change in weekly epoetin dosage, Mean absolute change in weekly epoetin dosage per kg body weight from baseline to 24 weeks after treatment with EPIAO®/EPREX® in parallel groups (IU/kg/week)., 24 weeks|Frequency of adverse events, To observe the frequency of adverse events following EPIAO® and EPREX® administration., 52 weeks|Occurence of anti-epoetin antibodies, To monitor the occurrence of anti-epoetin antibodies among subjects following at least 52 weeks of therapy., 52 weeks
Sponsor/Collaborators: Sponsor: Shenyang Sunshine Pharmaceutical Co., LTD. | Collaborators: Navitas Life Sciences GmbH
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 16
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2015-08
Completion Date: 2019-08
Results First Posted:
Last Update Posted: 2020-10-22
Locations: Bamrasnaradura Infectious Disease Institute, Bangkok, 10700, Thailand|Bhumibol Adulyadej hospital, Bangkok, 10700, Thailand|BMA hospital, Bangkok, 10700, Thailand|Chulalongkorn King Memorial hospital, Bangkok, 10700, Thailand|Klongton Hospital, Bangkok, 10700, Thailand|Phramongkutklao hospital, Bangkok, 10700, Thailand|Rajavithi hospital, Bangkok, 10700, Thailand|Siriraj Hospital, Bangkok, 10700, Thailand
URL: https://clinicaltrials.gov/show/NCT02522975