- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03350321
A Study of Molidustat for Correction of Renal Anemia in Non-dialysis Subjects (MIYABI ND-C)
January 28, 2021 updated by: Bayer
A Randomized, Open-label, Active-controlled, Parallel-group, Multicenter Study to Investigate the Efficacy and Safety of Oral Molidustat in Comparison to Darbepoetin Alfa in Non-dialysis Subjects With Renal Anemia Who Are Not Treated With Erythropoiesis-Stimulating Agents (ESAs)
The purpose of this study is to evaluate the efficacy and safety of molidustat in non-dialysis subjects with renal anemia who are not treated with Erythropoiesis-Stimulating Agents (ESAs).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
162
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Fukui, Japan, 910-8526
- Fukui Prefectural Hospital
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Fukuoka, Japan, 810-8563
- National Hospital Organization Kyushu Medical Center
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Fukuoka, Japan, 812-8582
- Kyushu University Hospital
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Fukuoka, Japan, 814-0180
- Fukuoka University Hospital
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Fukushima, Japan, 960-1295
- Fukushima Medical University Hospital
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Gifu, Japan, 500-8523
- Asahi University Hospital
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Kochi, Japan, 780-8077
- National Hospital Organization Kochi National Hospital
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Nara, Japan, 630-8581
- Nara Prefecture General Medical Center
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Oita, Japan, 870-0033
- Japanese Red Cross Oita Hospital
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Osaka, Japan, 543-8555
- Osaka Red Cross Hospital
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Osaka, Japan, 540-0006
- National Hospital Organization Osaka National Hospital
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Osaka, Japan, 558-8558
- Osaka General Medical Center
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Osaka, Japan, 530-8480
- Kitano Hospital
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Osaka, Japan, 550-0006
- Nippon Life Hospital
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Osaka, Japan, 555-0001
- Chibune Clinic
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Osaka, Japan, 559-0012
- Social Corporation Keigakukai Minamiosaka Hospital
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Shizuoka, Japan, 424-0855
- Suruga Clinic
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Shizuoka, Japan, 422-8527
- Shizuoka Saiseikai General Hospital
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Wakayama, Japan, 641-8510
- Wakayama Medical University Hospital
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Aichi
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Yatomi, Aichi, Japan, 498-8502
- Kainan Hospital
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Chiba
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Matsudo, Chiba, Japan, 271-0077
- Seikeikai New Tokyo Heart Clinic
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Ehime
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Matsuyama, Ehime, Japan, 791-8026
- Saiseikai Matsuyama Hospital
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Matsuyama, Ehime, Japan, 790-0024
- Ehime Prefectural Central Hospital
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Fukuoka
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Iizuka, Fukuoka, Japan, 820-8505
- Iizuka Hospital
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Kitakyushu, Fukuoka, Japan, 802-8555
- Kokura Memorial Hospital
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Kitakyushu, Fukuoka, Japan, 805-8508
- Steel Memorial Yawata Hospital
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Koga, Fukuoka, Japan, 811-3195
- National Fukuoka-Higashi Medical Center
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Kurume, Fukuoka, Japan, 830-8543
- St.Mary's Hospital
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Kurume, Fukuoka, Japan, 830-0011
- Kurume University Hospital
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Gifu
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Hashima-gun, Gifu, Japan, 501-6061
- Matsunami Health Promotion Clinic
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Tajimi, Gifu, Japan, 507-8522
- Gifu Prefectural Tajimi Hospital
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Hiroshima
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Aki-gun, Hiroshima, Japan, 735-8585
- Mazda Hospital of Mazda Motor Corporation
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Fukuyama, Hiroshima, Japan, 721-0927
- Nippon Kokan Fukuyama Hospital
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Hokkaido
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Sapporo, Hokkaido, Japan, 006-8555
- Teine Keijinkai Clinic
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Hyogo
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Kobe, Hyogo, Japan, 650-0047
- Kobe City Medical Center General Hospital
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Kobe, Hyogo, Japan, 654-0155
- National Hospital Organization Kobe Medical Center
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Ibaraki
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Higashiibaraki, Ibaraki, Japan, 311-3193
- National hospital Organization Mito Medical Center
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Mito, Ibaraki, Japan, 310-0015
- Mito Kyodo General Hospital
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Kagawa
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Takamatsu, Kagawa, Japan, 761-1701
- KenAiKai medical corporation Akiyama clinic
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Kagoshima
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Kanoya, Kagoshima, Japan, 893-0024
- Ikeda Hospital
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Kanagawa
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Fujisawa, Kanagawa, Japan, 251-8550
- Fujisawa City Hospital
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Kawasaki, Kanagawa, Japan, 210-0852
- Koukan Clinic
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Yokohama, Kanagawa, Japan, 227-8501
- Showa University Fujigaoka Hospital
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Yokosuka, Kanagawa, Japan, 238-8558
- Yokosuka Kyosai Hospital
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Kumamoto
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Arao, Kumamoto, Japan, 864-0041
- Arao Municipal Hospital
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Yatsushiro, Kumamoto, Japan, 866-8533
- Kumamoto Rosai Hospital
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Kyoto
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Uji, Kyoto, Japan, 611-0041
- Uji-Tokushukai Medical Center
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Mie
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Yokkaichi, Mie, Japan, 510-0016
- JCHO Yokkaichi Hazu Medical Center
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Miyagi
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Ishinomaki, Miyagi, Japan, 986-8522
- Japanese Red Cross Ishinomaki Hospital
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Nagano
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Komoro, Nagano, Japan, 384-8588
- Asama Nanroku Komoro Medical Center
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Niigata
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Shibata, Niigata, Japan, 957-8588
- Niigata Prefectural Shibata Hospital
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Okinawa
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Uruma, Okinawa, Japan, 904-2293
- Okinawa prefectural Chubu Hospital
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Osaka
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Suita, Osaka, Japan, 565-0862
- Osaka Saiseikai Senri Hospital
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Tondabayashi, Osaka, Japan, 584-0082
- Osaka Pref. Saiseikai Tondabayashi Hospital
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Saitama
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Kitamoto, Saitama, Japan, 364-8501
- Kitasato University Medical Center
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Shizuoka
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Iwata, Shizuoka, Japan, 438-8550
- Iwata City Hospital
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Tokyo
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Itabashi-ku, Tokyo, Japan, 173-8610
- Nihon University Itabashi Hospital
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Itabashi-ku, Tokyo, Japan, 173-0015
- Toshima Hospital
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Koto-ku, Tokyo, Japan, 135-8577
- Showa University Koto Toyosu Hospital
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Meguro-ku, Tokyo, Japan, 152-8902
- National Hospital Organization Tokyo Medical Center
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Yamanashi
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Chuo, Yamanashi, Japan, 409-3898
- University of Yamanashi Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects with estimated glomerular filtration rate (eGFR)< 60 mL/min/1.73m^2 (Chronic kidney disease [CKD] stages 3 to 5)
- Body weight > 40 and ≤ 160 kg at screening
- Male or female subject ≥ 20 years of age at screening
- Not on dialysis and not expected to start dialysis during the study period
- Not treated with ESAs and/or HIF-PH inhibitors within 8 weeks prior to randomization
- Mean of the last 2 central laboratory Hb levels during the screening period must be ≥ 8.0 and < 11.0 g/dL (2 measurements must be taken ≥ 2 days apart and the difference between the 2 measurements must be < 1.2 g/dL) and the last measurements must be taken within 14 days prior to randomization
- Ferritin ≥ 50 ng/mL at screening
Exclusion Criteria:
- New York Heart Association (NYHA) Class III or IV congestive heart failure
- History of cardio- (cerebro-) vascular events (e.g., unstable angina, myocardial infarction, stroke, pulmonary thromboembolism, and acute limb ischemia) within 6 months prior to randomization
- Sustained and poorly controlled arterial hypertension (defined as systolic BP≥ 180mmHg or diastolic BP ≥ 110mmHg) or hypotension (defined as systolic BP < 90mmHg) at randomization
- Proliferative choroidal or retinal disease, such as neovascular age-related macular degeneration or proliferative diabetic retinopathy requiring invasive treatment (e.g., intraocular injections or laser photocoagulation)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Molidustat (BAY85-3934)
Molidustat group
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Starting dose of molidustat once daily (OD) will be titrated based on the subject's Hb (Hemoglobin) response
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ACTIVE_COMPARATOR: Darbepoetin alfa
Darbepoetin alfa group
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Starting dose of darbepoetin alfa once every 2 weeks will be titrated based on the subject's Hb (Hemoglobin) response
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Mean Hb (Hemoglobin) level
Time Frame: From week 30 to 36
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From week 30 to 36
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Change in hemoglobin level from baseline to the average during the evaluation period
Time Frame: Baseline and week 30 to 36
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Baseline and week 30 to 36
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Hb level
Time Frame: Baseline and up to 52 weeks
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Baseline and up to 52 weeks
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Proportion of subjects with hemoglobin levels in the target range
Time Frame: Up to 52 weeks
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Up to 52 weeks
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Proportion of subjects with hemoglobin levels above the target range
Time Frame: Up to 52 weeks
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Up to 52 weeks
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Proportion of subjects with hemoglobin levels below the target range
Time Frame: Up to 52 weeks
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Up to 52 weeks
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Proportion of subjects whose maximum rise in Hb between each consecutive visits is above 0.5 g/dL/week
Time Frame: Up to 52 weeks
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Defined as change in Hb level / duration between two visits (weeks)
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Up to 52 weeks
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Number of participants with serious adverse events
Time Frame: Up to 52 weeks
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Up to 52 weeks
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Responder rate: proportion of responders among the subjects
Time Frame: From week 30 to 36
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Responder is defined as meeting all of the following criteria: (i) Mean of the Hb levels in the target range (ii) ≥ 50% of the Hb levels in the target range (iii) No rescue treatment |
From week 30 to 36
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Rate of rise in Hb (Hemoglobin) level (g/dL/week)
Time Frame: Up to 8 weeks
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Up to 8 weeks
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Rate of rise in Hb (Hemoglobin) level (g/dL/week)
Time Frame: Up to 4 weeks
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Up to 4 weeks
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Proportion of subjects who meet each component of the response
Time Frame: From week 30 to 36
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Response: (i) Mean of the Hb levels in the target range (ii) ≥ 50% of the Hb levels in the target range (iii) No rescue treatment |
From week 30 to 36
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Cumulative proportion of subjects who achieve the lower limit of the target Hb range at least once
Time Frame: Up to 52 weeks
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Up to 52 weeks
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Hb level
Time Frame: Baseline and up to 52 weeks
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Baseline and up to 52 weeks
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Proportion of subjects whose mean hemoglobin level is in the target range
Time Frame: From week 30 to 36
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From week 30 to 36
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|
Proportion of subjects whose mean hemoglobin level is above the target range
Time Frame: From week 30 to 36
|
From week 30 to 36
|
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Proportion of subjects whose mean hemoglobin level is below the target range
Time Frame: From week 30 to 36
|
From week 30 to 36
|
|
Maximum concentration (Cmax)
Time Frame: At baseline, week 12, week 24 and week 52
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At baseline, week 12, week 24 and week 52
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Area under the concentration-time curve (AUC)
Time Frame: At baseline, week 12, week 24 and week 52
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At baseline, week 12, week 24 and week 52
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EPO (Erythropoietin) serum concentration
Time Frame: At baseline, week 12, week 24 and week 52
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At baseline, week 12, week 24 and week 52
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Natale P, Palmer SC, Jaure A, Hodson EM, Ruospo M, Cooper TE, Hahn D, Saglimbene VM, Craig JC, Strippoli GF. Hypoxia-inducible factor stabilisers for the anaemia of chronic kidney disease. Cochrane Database Syst Rev. 2022 Aug 25;8(8):CD013751. doi: 10.1002/14651858.CD013751.pub2.
- Yamamoto H, Taguchi M, Matsuda Y, Iekushi K, Yamada T, Akizawa T. Molidustat for the treatment of renal anaemia in patients with non-dialysis-dependent chronic kidney disease: design and rationale of two phase III studies. BMJ Open. 2019 Jun 14;9(6):e026704. doi: 10.1136/bmjopen-2018-026704.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
December 12, 2017
Primary Completion (ACTUAL)
May 17, 2019
Study Completion (ACTUAL)
October 11, 2019
Study Registration Dates
First Submitted
November 19, 2017
First Submitted That Met QC Criteria
November 19, 2017
First Posted (ACTUAL)
November 22, 2017
Study Record Updates
Last Update Posted (ACTUAL)
January 29, 2021
Last Update Submitted That Met QC Criteria
January 28, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19349
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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