TY - JOUR
T1 - Rationale and Design of the Double-Blind, Randomized, Placebo-Controlled Multicenter Trial on Efficacy of Early Initiation of Eplerenone Treatment in Patients with Acute Heart Failure (EARLIER)
AU - Asakura, Masanori
AU - Yamamoto, Haruko
AU - Asai, Kuniya
AU - Hanatani, Akihisa
AU - Hirata, Ken ichi
AU - Hirayakma, Atsushi
AU - Kimura, Kazuo
AU - Kobayashi, Youichi
AU - Momomura, Shin ichi
AU - Nakagawa, Yoshihisa
AU - Nishi, Yutaro
AU - Saito, Yoshihiko
AU - Satoh, Yasuhiro
AU - Yamada, Takahisa
AU - Yamashina, Akira
AU - Yasuda, Satoshi
AU - Yoshikawa, Tsutomu
AU - Kada, Akiko
AU - Uesaka, Hiroyuki
AU - Kitakaze, Masafumi
N1 - Funding Information:
The other important characteristic of this study is that this is the first investigator-initiated phase III trial sponsored by multiple centers and funded by the Japanese government (the Ministry of Health, Labour and Welfare: MHLW). Japanese investigators in the cardiovascular fields have performed many large scale clinical trials including our previous study, J-WIND trial [], but unfortunately they are not phase III trials and are performed independently of the Pharmaceuticals and Medical Devices Agency (PMDA)/MHLW acting as the Japanese FDA. Therefore, even if the data are positive, the drug cannot be approved. We have been requested to conduct the investigator-initiated phase III trial in Japan, which is a global standard worldwide for the tight linkage between investigators and PMDA. When we use this framework to generate clinical data to be used for Japan marketing authorization, it has to comply with Japanese local Good Clinical Practice (J-GCP), which is required by the Japan pharmaceutical law. If the data of the present study meet the PMDA requirements and conform to J-GCP, eplerenone will be officially used for Japanese patients with ADHF. Therefore, we should be successful at least in the completion of this study and hopefully prove the evidence of the effectiveness of this compound for patients with ADHF. The favorable result would represent a hope for patients with ADHF worldwide, offering the possibility of recovery from damage to the heart. Acknowledgments Funding Conflict of interest
Funding Information:
MK, KA, KH, KK, YK, YS and AY received honorarium form Pfizer Japan. MK 、AH and YS received the research funding from Pfizer Japan. MK and TY is advisory board members of clinical trial on eplerenone in chronic heart failure (A6141114).
Publisher Copyright:
© 2015, Springer Science+Business Media New York.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Methods: EARLIER is an event-driven clinical trial with an estimated enrolment of 300 patients hospitalized with ADHF with reduced left ventricular ejection fraction. ADHF includes ischemic or non-ischemic HF, and patients can be enrolled within 72 h after the visit to the hospital. We randomize the patients taking standard therapies for ADHF to the eplerenone and placebo groups. Eplerenone, either 25 or 50 mg, is administered for 6 months in the eplerenone group, and the corresponding placebo is administered in the placebo group on top of the standard care. We set the primary endpoint as the incidence of the composite endpoint (cardiac death or first re-hospitalization due to cardiac disease) 6 months after the enrollment, and also check the quality of life, i.e., exercise capacity and safety features of eplerenone.Background and Aims: Aldosterone is one of the major factors to cause organ damage during an acute phase of heart failure (HF), and many reports have demonstrated that patients with acute decompensated HF (ADHF) have high blood aldosterone concentrations, and the high aldosterone concentrations predict poor prognosis in patients with HF. These findings suggest that eplerenone, an antagonist of aldosterone receptors may provide a new concept and strategy for the treatment of ADHF, protecting the heart and other organs during chronic phases, depending on the restoration of hemodynamic abnormalities.Conclusion and Perspectives: EARLIER is a clinical trial of eplerenone targeting ADHF and also the first multicenter investigator-initiated phase III trial in the cardiovascular field in Japan, funded by the Japanese government.
AB - Methods: EARLIER is an event-driven clinical trial with an estimated enrolment of 300 patients hospitalized with ADHF with reduced left ventricular ejection fraction. ADHF includes ischemic or non-ischemic HF, and patients can be enrolled within 72 h after the visit to the hospital. We randomize the patients taking standard therapies for ADHF to the eplerenone and placebo groups. Eplerenone, either 25 or 50 mg, is administered for 6 months in the eplerenone group, and the corresponding placebo is administered in the placebo group on top of the standard care. We set the primary endpoint as the incidence of the composite endpoint (cardiac death or first re-hospitalization due to cardiac disease) 6 months after the enrollment, and also check the quality of life, i.e., exercise capacity and safety features of eplerenone.Background and Aims: Aldosterone is one of the major factors to cause organ damage during an acute phase of heart failure (HF), and many reports have demonstrated that patients with acute decompensated HF (ADHF) have high blood aldosterone concentrations, and the high aldosterone concentrations predict poor prognosis in patients with HF. These findings suggest that eplerenone, an antagonist of aldosterone receptors may provide a new concept and strategy for the treatment of ADHF, protecting the heart and other organs during chronic phases, depending on the restoration of hemodynamic abnormalities.Conclusion and Perspectives: EARLIER is a clinical trial of eplerenone targeting ADHF and also the first multicenter investigator-initiated phase III trial in the cardiovascular field in Japan, funded by the Japanese government.
KW - Acute heart failure
KW - Acute myocardial infarction
KW - Aldosterone
KW - Cardiac death
KW - Eplerenone
KW - Re-hospitalization
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U2 - 10.1007/s10557-014-6565-2
DO - 10.1007/s10557-014-6565-2
M3 - Article
C2 - 25566817
AN - SCOPUS:84939978840
SN - 0920-3206
VL - 29
SP - 179
EP - 185
JO - Cardiovascular Drugs and Therapy
JF - Cardiovascular Drugs and Therapy
IS - 2
ER -