- Research article
- Open Access
Efficacy, tolerability and safety of darbepoetin alfa injection for the treatment of anemia associated with chronic kidney disease (CKD) undergoing dialysis: a randomized, phase-III trial
BMC Nephrology volume 20, Article number: 90 (2019)
Darbepoetin alfa (DA-α) is a long-acting erythropoiesis-stimulating glycoprotein which has half-life three-fold longer than that of Erythropoietin alfa (EPO). The objective of this study was to compare the efficacy and safety of DA-α injection versus EPO for treating renal anemia amongst Indian patients with end-stage renal disease (ESRD) undergoing dialysis.
Patients of either gender (aged 18–65 years) with ESRD undergoing dialysis who had hemoglobin (Hb) levels < 10 g/dL after receiving EPO were switched to DA-α (0.45 μg/kg) once weekly subcutaneously or EPO 50 IU/kg thrice weekly subcutaneously (centrally randomized 1:1) for 12–24 weeks (correction phase) followed by 12 weeks maintenance phase (for Hb levels ≥10 g/dL). The primary efficacy endpoint was mean change in Hb level from baseline to end of correction phase.
In the intention-to-treat population (n = 126), the between group difference in mean Hb change was − 0.01 g/dL (95% CI – 0.68 to − 0.66, p = 0.97). After adjusting for covariates, the difference was − 0.2878 g/dL (95% CI -0.936 to0.360). The lower limit of the two-sided 95% CI of primary endpoint was above the pre-specified non-inferiority margin of − 1.0 g/dL. Similar trend of non-inferiority was observed for per-protocol population. Safety profile of DA-α and EPO were observed to be similar.
Our study results demonstrated that for patients with ESRD undergoing dialysis, administering DA-α at lower dose frequency, is equally effective and well tolerated as EPO for treating renal anemia.
CTRI/2012/07/002835 [Registered on: 27/07/2012]; Trial Registered Prospectively.
Anemia is an inevitable complication of chronic kidney disease (CKD) and is caused predominantly by insufficient production of erythropoietin from the failing kidneys and circulating levels of erythropoietin [1,2,3]. In patients with CKD, untreated anemia has been associated with poor outcomes such as deterioration of cardiac function, decreased cognition, mental acuity, fatigue, and mortality [2,3,4,5].
Erythropoietin alfa (EPO) is a short acting erythropoiesis-stimulating agent (ESA) and has been a primary choice for treating anemia in patients with CKD for the past twenty years . EPO is approved for the correction of anemia in patients with chronic renal failure, and its use in renal anemia eliminates the need for red cell transfusions, alleviates the symptoms of anemia, improves survival, reduces cardiovascular morbidity, and enhances the quality of life [6, 7]. However, its optimal route of administration and dosage are debatable due to its short half-life . Intravenous (IV) administration of EPO should be limited to haemodialysis patients at a dosage of three times per week, as any dose reduction can lead to a major increase in the dose requirement . In addition, high doses of epoetin alfa increase the risk of poor outcomes including cardiovascular events . On the other hand, subcutaneous (sc) EPO therapy is efficacious during hemodialysis, peritoneal dialysis, and pre-dialysis in patients with CKD . The frequent dosing regimen of EPO poses a constant strain on patients and health care staff. Thus, long-acting ESAs are favored over short-acting ESAs .
Darbepoetin alfa (DA-α manufactured by Hetero Biopharma) is the first long-acting ESA with extended dosing intervals and thus has an advantage over epoetins alfa and beta. DA-α has played an important role in the effective management of anemia and is preferred over epoetins/biosimilar epoetins for patients requiring less-frequent administration of ESAs . DA-α owing to its longer half-life, maintains target hemoglobin levels (10-12g/dL) with low dosing frequency (once weekly or biweekly), benefiting patients and health care staff equally [6,7,8,9]. The dose requirement of EPO by the sc route was 22% lesser than that by the IV route; however, DA-α has similar dose requirements by both the sc and IV routes, which simplifies management of anemia .
Clinical studies have shown that DA-α administered once every 2 weeks or every month improves convenience and saves costs with no compromise in its efficacy while maintaining the target hemoglobin (Hb) range in patients . Therefore, this study aimed to determine whether a biosimilar DA-α has similar efficacy and safety as that of EPO when given at a reduced dose frequency for the treatment of renal anemia in Indian patients with end-stage renal disease (ESRD) undergoing dialysis.
The manuscript has been prepared as per CONSORT extension for non-inferiority and equivalence trial.
Study design and patient selection
This was a prospective phase III, randomized, open label, two-arm, parallel group, multi-center, active-controlled, noninferiority clinical study performed at 14 nephrology centers in India during Sept 2012–May 2014. Permuted block randomization schedule with block of size 4 and ratio of 1:1 in the two groups was generated using SAS® software version 9.1. The study was not blinded because of highly varying dosing schedules in the treatment groups. In this study, clinically stable patients (M/F) aged 18–65 years who were on hemodialysis or peritoneal dialysis for at least 4 weeks and had baseline Hb levels < 12 g/dL, were enrolled. Study included patients who were on EPO (not within 1 week before screening) or those who were EPO - naive, and had adequate serum ferritin (≥ 200 ng/mL) and transferrin saturation (≥ 20%) levels. Major exclusion criteria were congestive heart failure, history of uncontrolled hypertension (not amenable two standard drugs over 2 weeks of screening period), severe hyperparathyroidism, pregnant women or lactating mothers, diabetes with HbA1C ≥ 10%, systemic hematological diseases, liver disease, reported hypersensitive to any active study drug substances, or infections. During the study Vitamin B12 and red cell folate concentrations were tested at screening, week 12, end of correction phase and end of maintenance phase. Iron tests i.e. Serum Ferritin, Iron, TIBC, and TSAT were measured at screening, weeks 4, 8, 12, 16, 20, 24 and end of maintenance. Inflammatory marker (CRP) is measured at screening.
The study treatment comprised correction phase (12 to 24 weeks) and maintenance phase (24 to 36 weeks). During 12-24 weeks of correction phase, at baseline, the patients having Hb levels < 10 g/dL with EPO, were switched to either DA-α once weekly (0.45 μg/kg subcutaneous injection manufactured by Hetero Biopharma Limited, India) or EPO thrice weekly (50 IU/kg, Eprex® manufactured by Cilag AG, Switzerland) in allocation ratio of 1:1. The patients with treatment failure, i.e those who had Hb level < 10 g/dL at the end of correction phase (EOC), were discontinued from the study. Following EOC phase, the patients with Hb levels ≥10 g/dL were switched to DA-α for 12 weeks of maintenance phase. If the dialysis patients had Hb level ≥ 10 g/dL at baseline, they directly entered the maintenance phase and were randomized (1:1) to receive DA-α (0.45 μg/kg) once weekly or EPO (50 IU/kg) thrice weekly. In both of the treatment arms, appropriate dose adjustments were made to achieve and maintain patients’ Hb level within the target range, i.e ≥ 1 g/dL increase from baseline Hb, and within the range of 10–12 g/dL during the 36-week study period. Dosage was increased by 25% if a patient’s Hb remained < 10 g/dL even after achieving the target range during the correction phase. In the maintenance phase, if the patient’s Hb levels went above the target range (≥ 11.5 g/dL) for two consecutive weekly assessments, the dosage was decreased by 25%. The dosage was increased by 25%, if after achieving the target range (10–12 g/dL), patient’s Hb level was below 10 g/dL. There was no specific rescue therapy defined in the study protocol. However, Iron supplements (oral/IV) were allowed as concomitant medication to prevent apparent iron deficiency. For patients with serum ferritin values < 100 μg/L or ≥ 100 μg/L, the IV iron dosing regimen was determined per the individual center’s treatment protocol.
Efficacy and safety assessments
Hemoglobin (Hb) levels were assessed throughout the correction and maintenance phases. Primary efficacy endpoint included the mean change in Hb level from baseline at the first evaluation visit (EOC) in patients treated with EPO versus DA-α. Secondary efficacy endpoints were Hb variability during correction phase, mean change in Hb levels from baseline to week-4 and week-36 (EOM), proportion of patients achieving the Hb target (defined as Hb increase ≥ 1 g/dL from baseline) at EOC, mean DA-α dose, proportion of patients who could maintain the target Hb of 10–12 g/dL at EOM, and time to initial achievement of Hb target. Safety assessment included serum chemistry, complete blood count, and urinalysis measured at baseline and after treatment. Adverse events (AEs) were monitored at each study visit. Safety endpoints were the incidence of treatmentemergent adverse events (TEAEs) and immunogenicity as assessed by anti-drug antibody titers using ELISA methods. Samples for immunogenicity to DA-α/EPO were withdrawn within 1 h of dosing before initial dosing, i.e Day 1 of week 1 and on day 1 of weeks 5, 13, 25 and EOM. Since the screening time and evaluation periods of the various patient subgroups were different, the time points for immunogenicity varied accordingly.
Assuming an estimated difference between the treatments of − 0.5 g/dL in mean change in Hb levels with a noninferiority margin at − 1.0 g/dL, to achieve 80% power for the non-inferiority test, a total of 100 patients are required to be allocated in the ratio of 1:1 to either DA-α (n = 50) or EPO (n = 50). A final sample size of 126 patients (63 patients in each treatment arm) was derived assuming dropout rate at 20%. A designated statistician (Sristek, India) generated the allocation sequence and assigned participants to their groups, and investigators at 14 nephrology sites enrolled participants according to this sequence. Efficacy analysis included both the intent to treat (ITT) and per protocol (PP) population. ITT population comprised randomized patients who received at least one dose of the study drug, with baseline and at least one efficacy assessment available during the evaluation period. PP set included patients who completed all the study visits as defined in the protocol without major protocol deviations. Safety population comprised all randomized patients who received at least one dose of the study drug. The between group difference in the mean Hb change from baseline to first evaluation visit was analyzed using analysis of covariance (ANCOVA). Treatment was considered as main effect and baseline Hb levels as the covariate in the model. The two-sided 95% CI for difference in mean Hb for treatments was calculated to assess the non-inferiority, and if it was above the non-inferiority margin of − 1.0 g/dL, the non-inferiority was accepted. Two sample t-tests at 5% level of significance were performed to compare the difference of change in Hb level from baseline to week-4 and week-36 EOM. For all tests, p-value of ≤ 0.05 was considered as statistically significant. Logistic regression was carried out to compare the proportion of patients achieving the Hb target (≥ 1 g/dL from baseline and Hb concentration of 10–12 g/dL) at the end of first evaluation visit and EOM. The time to the initial achievement of Hb target at the EOC was estimated using Kaplan-Meier. SAS® Version 9.4 (SAS Institute Inc., USA) was used to perform all statistical analyses.
Patient disposition and baseline characteristics
A total of 213 patients who underwent dialysis were screened for anaemia (Fig. 1). Of these, a total of 126 patients (63 patients in each group) who met the eligibility criteria were enrolled and randomized (ITT population). The PP population consisted of 107 patients, of which 93 patients were in correction phase due to Hb level < 10 g/dL at screening or baseline, 14 patients directly entered into the maintenance phase due to Hb level > 10 g/dL at screening and baseline who were on EPO (thrice weekly/biweekly) during screening & baseline phase. The demographic characteristics of the safety population are given in Table 1. Patient’s flow in the study as well as schematic diagram of the study elaborated in Figs. 1 and 2, respectively. Majority of patients were male in both the treatment groups, where the mean (± SD) age of enrolled patients was 46.8 (± 12.32). The mean (± SD) dose of DA-α was 26.12 (± 0.98) μg at week 1 and 27.73 (± 1.62) μg at week 12. The mean (± SD) dose of EPO at week 1 and 12 was 3038.3 (± 115.42) IU and 2998.7 (± 221.23) IU, respectively.
In ITT population, Hb levels were increased gradually from baseline to the end of first evaluation period, with the mean change in Hb levels of 1.84 and 1.85 in DA-α and EPO group, respectively (within group comparison, p < 0.001 for each). Change from baseline to the end of first evaluation period in Hb levels was equal in PP population for both treatment groups. The mean Hb change from baseline to the first evaluation period was equal in both, DA-α (1.84; 95% CI 1.36 to 2.32) and EPO (1.85; 95% CI 1.37 to 2.33) groups (Table 2). The difference in the mean change in Hb levels amongst the two groups was − 0.01 g/dL (95% CI − 0.68 to − 0.66, p = 0.97). The difference was not statistically significant even with the low frequency of DA-α administration (Table 2).
The difference in the mean Hb change amongst the two groups was − 0.2878 g/dL (95% CI − 0.936 to − 0.360) when adjusted for covariates (using ANCOVA) (Table 3). The lower limit of the two-sided 95% CI of primary endpoint was above the pre-specified non-inferiority margin of − 1.0 g/dL, irrespective of being adjusted (− 0.936) or unadjusted (− 0.68) for covariates, establishing that DA-α was equally effective as EPO, in maintaining mean Hb despite the reduced dosing frequency in patients undergoing dialysis. The results of PP population analysis set further confirmed the robustness of ITT analysis (Tables 2 and 3). In PP population, the lower limit of the 95% CI was − 0.994 (adjusted) and − 0.81 (unadjusted), which was above the pre-specified non-inferiority margin of − 1.0 g/dL.
Improvement in Hb levels was observed as early as week 4 in both treatment groups which showed similar mean Hb change in the DA-α (0.30 g/dL, 95% CI − 0.01 to − 0.61, p = 0.0566) and EPO (0.74 g/dL, 95% CI 0.29 to 1.19, p = 0.0019) groups (Table 4). The difference in mean Hb change between the two groups was − 0.44 g/dL (95% CI − 0.97 to − 0.09, p = 0.105), which was not statistically significant irrespective of the reduced frequency of DA-α administration. Increase in Hb levels from baseline was also similar in PP population even at week 4 (mean Hb change: − 0.62, 95% CI − 1.14 to − 0.10, p = 0.0209). The between group comparison at the end of second evaluation visit showed that the difference in mean Hb change was similar in both ITT (p = 0.94) and PP population (p = 0.88).
As summarized in Table 5, in ITT population, the similar proportions of patients were observed to achieve target Hb level at the end of the first evaluation visit (DA-α vs. EPO: 52.38% vs. 49.2%; OR [95% CI] = 0.96 [0.46 to 1.99], p = 0.90). Similar results was observed in PP population (DA-α vs. EPO: 68.08% vs. 69.56%; OR [95% CI] = 0.94 [0.39 to 2.30], p = 0.89). In ITT and PP population, the KM estimated median time to achieve the target Hb level was 9 weeks and 7 weeks after DA-α and EPO treatment, respectively. In ITT population, the proportion of patients who maintained their Hb levels within the target Hb range (10–12 g/dL) till the EOM was similar in both the treatment groups (DA-α vs. EPO: 38.10% vs. 57.14% respectively; OR [95% 314 CI] = 0.57 [0.26 to1.25], p = 0.16). Similar result was observed in PP population for both treatment groups (DA-α vs. EPO: 34.09% vs. 57.50% respectively; OR [95% CI] = 0.46 [0.17 to 1.22], p = 0.11). This demonstrates that, compared to EPO, DA-α does not increase Hb variability despite reducing the dosing frequency. Furthermore, fewer dose adjustments were observed in DA-α treated patients.
In the DA-α group, 25 (39.7%) patients and 32 (50.8%) patients in EPO group experienced at least one TEAE during the study period. Patients mostly reported TEAEs of mild-to-moderately severe in nature except one (1.58%) from the EPO group who experienced severe TEAEs. None from the DA-α group reported any TEAE related to the study drug; whereas, 4 patients from the EPO group reported 5 AE related to the study drug. In the EPO group, 4 patients reported 5 AEs that were related to the study drug. SAEs were reported by 9 patients (5 from EPO group and 4 from the DA-α group). The commonly reported events in both the treatment groups were pyrexia (DA-α vs. EPO: 9.5% vs. 7.9%), cough (9.5% vs. 15.9%), vomiting (4.8% vs. 6.3%), nasopharyngitis (4.8% vs. 6.3%), increased blood creatinine and urea (4.8% vs. 4.8% for each) and decreased glomerular filtration rate (4.8% vs. 4.8%). During the study, clinical laboratory evaluation of hematology, biochemistry and coagulation indicated no unexpected changes which could be attributed to the study drug. During the study, no changes in vital signs, mean blood pressure or heart rate were observed in either of the treatment groups.
Treatment emergent adverse events (TEAEs) were evaluated throughout the study. In DA-α group, the most commonly reported TEAEs by SOC were; respiratory, thoracic and mediastinal disorders (14.3%), general disorders and administration site conditions (12.7%), investigations (9.5%), and infections and infestations (7.9%). In EPO group, the most commonly reported TEAEs by SOC were; respiratory, thoracic and mediastinal disorders (22.2%), general disorders and administration site conditions (15.9%), vascular disorders (12.7%), gastrointestinal disorders (11.1%), infections and infestations (9.5%), and investigations (7.9%). There was no statistical difference between the two groups in terms of TEAEs.
Altogether, DA-α had a similar safety profile to that of EPO and no antibody formation was identified.
This randomized, active-controlled study aimed to compare the efficacy and safety of DA-α and EPO for the treatment of renal anemia among Indian patients with ESRD (end-stage renal disease) undergoing dialysis. This study achieved its primary efficacy, which demonstrates non-inferiority of DA-α over a most-widely used comparator, EPO. The results of this study demonstrated that, the efficacy of DA-α, when administered at reduced dose frequency, is similar to EPO for treating renal anaemia in patients undergoing dialysis. In this study, patients who were treated with DA-α could effectively maintain their Hb levels in the target therapeutic ranges and required with fewer dose adjustments than those treated with EPO. Therefore, the treatment using DA-α rules out the need for frequent monitoring and dose adjustments. In addition, both groups showed similar increases in Hb levels. Evaluating the iron availability for erythropoeisis is crucial in treating anaemia patients with CKD.Iron deficiency can interfere with the response to EPO and DA-α and affecting the efficacy. Thus, according to clinical practice guidelines and recommendations, iron supplements were given to all the patients in our study [4, 10]. To help maintain serum ferritin within recommended levels, most patients from both treatment arms received iron supplements. Additionally, serum ferritin levels were similar in both treatment groups.
In our study, DA-α (manufactured by Hetero Biopharma) was as safe as EPO. A majority of the reported AEs were due to the underlying disease and its treatment; in addition, only few AEs were associated with EPO use, and none were related to DA-α use. This study showed that safety profile of DA-α similar to those in other clinical trials conducted in pre dialysis stage of patients [11,12,13]. Also, it was observed that DA-α was well tolerated and had similar safety profile to EPO.
The results of our study demonstrated that efficacy and safety of DA-α (manufactured by Hetero Biopharma), when administered at a reduced dose frequency, is similar to EPO for treating renal anemia in Indian patients with ESRD undergoing dialysis.
Analysis of covariance
Chronic kidney disease
Enzyme linked immunosorbent assay
End of correction
End of maintenance
End-stage renal disease
Intent to treat
Treatment-emergent adverse events
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Authors would like to thank Darbepoetin investigator group (Dr. Abraham, Dr. Hegde, Dr. Parekh, Dr. Vakil, Dr. Goplani, Dr. Sajgure, Dr. Amitabh Anantrao Kulkarni, Dr. Dilip M Babu, Dr. A Anuradha, and Dr. Dinesh Khullar) for conducting this study. Authors would also like to thank all the study subjects for their valuable participation in this study. Authors also acknowledge CBCC Global Research LLP for their editorial support which was funded by Hetero Biopharma Limited, India.
This study was sponsored by Hetero Biopharma Limited, India including the study related materials and study drugs. The study was designed and executed by CRO partner assigned by Hetero Biopharma Limited, India in line with local and international regulatory requirement.
Availability of data and materials
Data supporting the findings are presented within the manuscript and additional datasets used are available from the corresponding author on request.
Ethics approval and consent to participate
The study was conducted in accordance with the ethical guidelines outlined in the Declaration of Helsinki, 1964 as revised in 2013. Institutional ethics committee approval was obtained (details given in the Additional file 1: Table S1) from each participating study center before initiating the study. Prior to conducting any study-related screening procedure, written informed consent was obtained from each patient before enrolling them in the study. The study was registered with the clinical trial registry (CTRI: CTRI/2012/07/002835) prior to any enrollment.
Consent for publication
SS1, VB, BB, PT and SC are the employees of Hetero Biopharma Limited, India and involved from conception of study to the approval of the manuscript. All the authors declare no other competing interests.
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Sinha, S.D., Bandi, V.K., Bheemareddy, B.R. et al. Efficacy, tolerability and safety of darbepoetin alfa injection for the treatment of anemia associated with chronic kidney disease (CKD) undergoing dialysis: a randomized, phase-III trial. BMC Nephrol 20, 90 (2019). https://doi.org/10.1186/s12882-019-1209-1
- Darbepoetin alfa
- End-stage renal disease