Anemia Studies in CKD: Erythropoiesis Via a Novel PHI Daprodustat - Pediatric (ASCEND-P)
NCT05682326
Anaemia, Anemia
Aichi, Japan
View Trial DetailsNCT Number: NCT02185911
To describe anaemia correction via haemoglobin measurements taken throughout observation period in ESA naive patients with chronic kidney disease initiated on darbepoetin alfa QM
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Notify Me18 year–100 year
All sexes
Observational
Research Site, Feldkirch, Austria
Darbepoetin alfa (Aranesp) is a long-acting ESA approved for treatment of anaemia in CKD patients, and may be administered once a week (QW), once every two weeks (Q2W) or once a month (QM) for correction and for maintenance in CKD patients not on dialysis. Prescribing information for darbepoetin alfa was updated in August 2013 (in EU and Australia), to incorporate the option for correction at QM dosing frequency in CKD patients not on dialysis. There is very little published literature describing QM correction in a real-world setting.
Data obtained from this study are intended to contribute to filling a literature gap and to provide a robust source of information for physicians.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: During the 32 weeks post initiation of darbepoetin alfa QM
Monthly Hb within 10-12g/dL during the 32 weeks post initiation of darbepoetin alfa QM
Time frame: Throughout the 46 week observation period
Doses of darbepoetin alfa/other ESAs over time (dose, route, frequency)
Time frame: Throughout the 46 week observation period
Haemoglobin over the observation period
Time frame: Throughout the 46 week observation period
Change in haemoglobin from baseline
Time frame: Throughout the 46 week observation period
Increase in haemoglobin of at least 1g/dL from baseline
Time frame: Throughout the 46 week observation period
Haemoglobin excursions (<10,>12 g/dL) over the observation period
Time frame: During the 32 weeks post initiation of darbepoetin alfa QM
Time from initiation of darbepoetin alfa QM to first haemoglobin within 10-12g/dL
Time frame: During the 32 weeks post initiation of darbepoetin alfa QM
Time from third dose of darbepoetin alfa at QM dosing frequency to first frequency change
Time frame: During the 32 weeks post initiation of darbepoetin alfa QM
Remaining on darbepoetin alfa QM for the full 32 weeks post initiation
Time frame: Throughout the 46 week observation period
TSAT, ferritin and albumin over the observation period
Time frame: Throughout the 46 week observation period
Iron use (dose/route) over the observation period
Time frame: Throughout the 46 week observation period
Transfusions over the observation period (number of tranfusions and the number of units transfused)
Time frame: Throughout the 46 week observation period
Hospitalisations (duration and primary cause) over the observation period
Amgen
Industry
Observational Study of Correction of Anaemia With Darbepoetin Alfa at Monthly Dose Frequency in EU and Australian Patients With Chronic Kidney Disease Not on Dialysis
Acronym: ADAPTATION
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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