Trial record 1 of 1 for:
20110226
Strategies Using Darbepoetin Alfa to Avoid Transfusions in Chronic Kidney Disease (START-CKD)
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| ClinicalTrials.gov Identifier: NCT01652872 |
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Recruitment Status :
Completed
First Posted : July 30, 2012
Results First Posted : November 8, 2018
Last Update Posted : December 12, 2018
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Sponsor:
Amgen
Information provided by (Responsible Party):
Amgen
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Brief Summary:
A phase 3, multicenter, randomized, double-blind, parallel group study. Anemic subjects with chronic kidney disease (CKD) and not on dialysis will be randomized 1:1 to 1 of 2 dosing strategies to evaluate the proportion of subjects receiving at least one red blood cell (RBC) transfusion. In the haemoglobin (Hb)-based titration group, darbepoetin alfa doses will be titrated to maintain Hb ≥ 10.0 grams/deciliter (g/dL). In the fixed dose group, subjects will receive a fixed dose of darbepoetin alfa. Treatment group, darbepoetin alfa doses, and protocol specified Hb concentrations will be blinded. Subjects will be followed for approximately 2 years from the date of randomization.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Anemia in Chronic Kidney Disease Patients Not on Dialysis | Biological: Darbepoetin alfa Other: Placebo | Phase 3 |
The study is a phase 3, multicenter, randomized, double-blind, parallel group study designed to describe the benefits and potential risks of a new treatment strategy using a fixed dose of darbepoetin alfa in subjects with CKD and not on dialysis. Anemic subjects without recent use of an erythropoiesis stimulating agent (ESA) will be randomly allocated 1:1 to treatment with a fixed dose of darbepoetin alfa or to treatment with darbepoetin alfa using a Hb-based titration strategy, which has been the conventional dosing strategy. In the Hb-based titration group, darbepoetin alfa doses will be titrated to maintain Hb ≥ 10.0 g/dL. This study aims to estimate the incidence of RBC transfusions (administered as deemed clinically necessary) in each group and the difference in incidence of RBC transfusions between the 2 groups. In addition, multiple aspects, such as cumulative darbepoetin alfa dose, total number of units of transfusions, Hb concentration, Hb-related parameters (eg, Hb variability, excursions, rate of change), and adverse (eg, cardiovascular) events, will also be considered in order to determine a preferred dosing regimen. Treatment group, darbepoetin alfa doses, and protocol specified Hb concentrations will be blinded to the investigator, subjects and study team. Subjects will be followed for approximately 2 years from the date of randomization.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 756 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Triple (Participant, Care Provider, Investigator) |
| Primary Purpose: | Treatment |
| Official Title: | Strategies Using Darbepoetin Alfa to Avoid Transfusions in Chronic Kidney Disease |
| Actual Study Start Date : | July 30, 2012 |
| Actual Primary Completion Date : | October 19, 2017 |
| Actual Study Completion Date : | October 19, 2017 |
Resource links provided by the National Library of Medicine
Drug Information available for:
Darbepoetin Alfa
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Hb-Based Titration Group
Participants received darbepoetin alfa as a subcutaneous (SC) injection once every 4 weeks (Q4W) for up to 96 weeks. The dose of darbepoetin alfa was titrated based on the Hb concentration on the date of the visit, the corresponding Hb rate of rise (ROR), and the previously assigned dose. Doses were reduced if Hb exceeded 10.5 g/dL or Hb ROR exceeded 1.0 g/dL/4W. When darbepoetin alfa therapy was withheld per the dosing algorithm, placebo was administered. The starting dose of darbepoetin alfa was 0.45 micrograms/kilogram (mcg/kg) and the protocol specified doses ranged from 10 to 300 mcg.
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Biological: Darbepoetin alfa
Darbepoetin alfa was presented as single use prefilled syringes (PFS). Investigational product was administered SC Q4W for the duration of the treatment period.
Other Name: Aranesp Other: Placebo Placebo was presented as single use PFS. Participants received a SC placebo injection in place of darbepoetin alfa therapy when the dose of study drug was withheld per the dosing algorithm for the duration of the treatment period. |
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Experimental: Fixed Dose Group
Participants received darbepoetin alfa as a SC injection Q4W at the same dose as assigned at the time of randomization for the duration of the 96 week treatment period. There was 1 exception to the fixed dose strategy: if the Hb was > 12.0 g/dL, darbepoetin alfa therapy was withheld and placebo administered. Once the Hb fell to < 10.0 g/dL, darbepoetin alfa therapy resumed at the same dose. The starting dose of darbepoetin alfa was 0.45 mcg/kg and the protocol specified doses ranged from 10 to 300 mcg.
|
Biological: Darbepoetin alfa
Darbepoetin alfa was presented as single use prefilled syringes (PFS). Investigational product was administered SC Q4W for the duration of the treatment period.
Other Name: Aranesp Other: Placebo Placebo was presented as single use PFS. Participants received a SC placebo injection in place of darbepoetin alfa therapy when the dose of study drug was withheld per the dosing algorithm for the duration of the treatment period. |
Primary Outcome Measures :
- Percentage of Participants in Receipt of 1 or More RBC Transfusions [ Time Frame: From randomization until the end of study, up to week 101. ]The percentage of participants receiving at least 1 RBC transfusion during the evaluation period was recorded for each treatment group. The evaluation period began from the date of randomization, and participants were censored at the last dose of investigational product plus 3 months or end of study, whichever was earlier (on-treatment approach).
Secondary Outcome Measures :
- Mean Number of Units of RBC Transfused [ Time Frame: From randomization until the end of study, up to week 101. ]The total number of units of RBC transfused per participant during the evaluation period was recorded for each treatment group. The evaluation period began from the date of randomization, and participants were censored at the last dose of investigational product plus 3 months or end of study, whichever was earlier (on-treatment approach). The mean total number of RBC units transfused per participant is presented.
- Time to First RBC Transfusion [ Time Frame: From randomization until the end of study, up to week 101. ]Time to first RBC transfusion during the evaluation period was recorded for each treatment group. The evaluation period began from the date of randomization, and participants were censored at the last dose of investigational product plus 3 months or end of study, whichever was earlier (on-treatment approach). The time to first RBC transfusion is presented using Kaplan-Meier (KM) estimates at 6, 12, 18, and 24 months.
- Mean Achieved Hb Concentration While Receiving Investigational Product [ Time Frame: From week 13 until the end of study, up to week 101. ]Average achieved Hb concentration while receiving investigational product was recorded as mean Hb using the area under the curve (AUC) method for each treatment group. The AUC of Hb was calculated according to the trapezoidal method, standardized as daily AUC. Participants with available Hb values from study day 85 (week 13) to the last dose date were included in the calculation.
- Geometric Mean Cumulative Dose of Darbepoetin Alfa Per 4 Weeks [ Time Frame: From randomization until the end of study, up to week 101. ]Cumulative doses of darbepoetin alfa adjusted for investigation product exposure time (e.g. mean cumulative darbepoetin alfa dose per 4 weeks) were calculated for each treatment group using the total cumulative dose during the study divided by total number of weeks dosed then multiplied by 4. The geometric mean cumulative dose is presented.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Key Inclusion Criteria:
- Clinical history of advanced CKD not on dialysis with at least 1 historic estimated glomerular filtration rate (eGFR) < 45.0 mL/mi)/1.73 m2 at least 12 weeks prior to screening
- Not currently receiving dialysis with an eGFR < 45.0 mL/min/1.73m2, per the central laboratory during screening
- Chronic anemia due to renal failure
- Two Hb concentrations < 10.0 g/dL, at least 2 weeks apart during screening using the modified Hb point of care (POC) device
- Iron replete, defined as a transferrin saturation (TSAT) ≥ 20% and a ferritin ≥ 100 ng/mL, per the central laboratory during screening
- Vitamin B12 and folate replete, defined as a vitamin B12 level > 180 pg/mL and a folate concentration > 7 nmol/L, per the central laboratory during screening
- Clinically stable in the opinion of the investigator
- Subject has provided written informed consent
Key Exclusion Criteria:
- Systemic hematologic disease (eg, sickle cell anemia, myelodysplastic syndrome, hematologic malignancy)
- Current or prior malignancy within 5 years of screening, with the exception of non-melanoma skin cancers and cervical intraepithelial neoplasia
- Treatment for any malignancy (eg, radiation, chemotherapy, hormone therapy, or biologics) within 5 years of screening, with the exception of locally excised non-melanoma skin cancer or cervical intraepithelial neoplasia
- Female subject not willing to use highly effective methods of birth control during treatment and for 4 weeks after the end of treatment
- Subject is pregnant or breast feeding, or might become pregnant during the study or within 4 weeks after the end of treatment
- Currently receiving intravenous (IV) antibiotics for treatment of an active infection
- Known Human Immunodeficiency Virus (HIV) positive
- Currently receiving systemic immunosuppressive therapy with the exception of prednis(ol)one ≤ 10 mg per day (or the steroid equivalent)
- History of any organ transplant
- Currently enrolled in another interventional study (eg, studies which require medical device use or drug therapy or with protocol required procedures), or less than 4 weeks since ending another interventional study(s) or receiving investigational agent(s)
- Known neutralizing anti-erythropoietic protein antibodies
- Known sensitivity to any of the products to be administered during dosing
- Previously enrolled in this study
- Not expected to be available for protocol required study visits or procedures to the best of the subject and investigator's knowledge
- Subject has any kind of disorder that, in the opinion of the investigator, may compromise the ability of the subject to give written informed consent and/or comply with all required study procedures
- Occurrence of stroke or myocardial infarction (MI) within 24 weeks of screening
- Receipt of RBC transfusion within 8 weeks of screening
- Occurrence of seizure, clinically relevant active bleeding (eg, gastrointestinal [GI] bleed) or any hospitalization within 8 weeks of screening
- Receipt of any IV iron therapy within 4 weeks of screening
- Changes in oral iron therapy within 4 weeks of screening
- Receipt of ESA therapy within 4 weeks of screening
- Diagnosis or treatment of malignancy, with the exception of non-melanoma skin cancers and cervical intraepithelial neoplasia during screening
- Receipt of ESA therapy, RBC transfusions, IV iron therapy during screening
- Changes in oral iron therapy during screening
- Occurrence of stroke, MI, seizure, clinically relevant active bleeding (eg, GI bleed), any hospitalization or outpatient surgery during screening
- Uncontrolled hypertension during screening. Defined in this study, as a mean systolic blood pressure > 140 mmHg at both screening visits, or a mean systolic blood pressure >/= 160 mmHg at any screening visit, or a mean diastolic blood pressure >/= 90 mmHg at any screening visit.
- Expected or scheduled change in oral iron therapy or receipt of IV iron therapy within 4 weeks after randomization
- Expected or scheduled receipt of a RBC transfusion within 8 weeks after randomization
- Expected or scheduled organ transplant within 24 weeks after randomization
- Expected or scheduled initiation of dialysis within 24 weeks after randomization
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01652872
Locations
Show 249 study locations
Sponsors and Collaborators
Amgen
Investigators
| Study Director: | MD | Amgen |
Study Documents (Full-Text)
Documents provided by Amgen:
Documents provided by Amgen:
Study Protocol [PDF] December 16, 2013
Statistical Analysis Plan [PDF] May 16, 2012
Additional Information:
| Responsible Party: | Amgen |
| ClinicalTrials.gov Identifier: | NCT01652872 |
| Other Study ID Numbers: |
20110226 |
| First Posted: | July 30, 2012 Key Record Dates |
| Results First Posted: | November 8, 2018 |
| Last Update Posted: | December 12, 2018 |
| Last Verified: | November 2018 |
Keywords provided by Amgen:
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anemia chronic kidney disease kidney disease renal failure |
Additional relevant MeSH terms:
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Kidney Diseases Renal Insufficiency, Chronic Urologic Diseases |
Renal Insufficiency Darbepoetin alfa Hematinics |