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The purpose of this study is to evaluate the efficacy and safety of Molidustat in dialysis subjects with renal anemia who are not treated with Erythropoiesis-Stimulating Agents (ESAs)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Molidustat (BAY85-3934) | Experimental | Molidustat group |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Molidustat (BAY85-3934) | Drug | Starting dose of molidustat once daily (OD) will be titrated based on the subject's Hb (Hemoglobin) response |
|
| Measure | Description | Time Frame |
|---|---|---|
| Rate of rise in Hb (Hemoglobin) level (g/dL/week) | Up to 8 weeks | |
| Responder rate: proportion of responders among the subjects | 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 | Week 21 to 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of rise in Hb (Hemoglobin) level (g/dL/week) | Up to 4 weeks | |
| Proportion of subjects who meet each component of the response | 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Houshikai Kano hospital | Kasuya-gun | Fukuoka | 811-0120 | Japan | ||
| Matsunami General Hospital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33506635 | Derived | Akizawa T, Nobori K, Matsuda Y, Hayashi Y, Hayasaki T, Yamamoto H. Molidustat for anemia correction in Japanese patients undergoing hemodialysis: a single-arm, phase 3 study. Ther Apher Dial. 2021 Dec;25(6):917-925. doi: 10.1111/1744-9987.13627. Epub 2021 Mar 22. | |
| 31203241 | Derived | Akizawa T, Taguchi M, Matsuda Y, Iekushi K, Yamada T, Yamamoto H. Molidustat for the treatment of renal anaemia in patients with dialysis-dependent chronic kidney disease: design and rationale of three phase III studies. BMJ Open. 2019 Jun 14;9(6):e026602. doi: 10.1136/bmjopen-2018-026602. |
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| ID | Term |
|---|---|
| D000740 | Anemia |
| D051436 | Renal Insufficiency, Chronic |
| ID | Term |
|---|---|
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
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| ID | Term |
|---|---|
| C000603972 | molidustat |
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| Week 21 to 24 |
| Cumulative proportion of subjects who achieve the lower limit of the target Hb range at least once at each visit | Up to 24 weeks |
| Hb level | Baseline and up to 24 weeks |
| Change in Hb level | Baseline and up to 24 weeks |
| Proportion of subjects whose mean hemoglobin levels are above the target range during the evaluation period | Week 21 to 24 |
| Proportion of subjects whose mean hemoglobin levels are below the target range during the evaluation period | Week 21 to 24 |
| Proportion of subjects whose mean hemoglobin levels are in the target range during the evaluation period | Week 21 to 24 |
| Proportion of subjects with hemoglobin levels above the target range | Up to 24 weeks |
| Proportion of subjects with hemoglobin levels below the target range | Up to 24 weeks |
| Proportion of subjects with hemoglobin levels in the target range | Up to 24 weeks |
| Proportion of subjects whose maximum rise in Hb between each consecutive visits is above 0.5 g/dL/week | Defined as change in Hb level / duration between two visits (weeks) | Up to 24 weeks |
| Number of participants with serious adverse events | Up to 24 weeks |
| Maximum concentration (Cmax) of Molidustat | Baseline, Week 8, Week16 and Week 24 |
| Area under the concentration-time curve (AUC) of Molidustat | Baseline, Week 8, Week16 and Week 24 |
| EPO (Erythropoietin) serum concentration of Molidustat | Baseline, Week 8, Week16 and Week 24 |
| Hashima-gun |
| Gifu |
| 501-6062 |
| Japan |
| Asahikawa-Kosei General Hospital | Asahikawa | Hokkaido | 078-8211 | Japan |
| Ishikari Hospital | Ishikari | Hokkaido | 061-3213 | Japan |
| Itami Kidney Clinic | Noboribetsu | Hokkaido | 059-0026 | Japan |
| Souen Central Hospital | Sapporo | Hokkaido | 060-0008 | Japan |
| Takasago Seibu Hospital | Takasago | Hyōgo | 676-0812 | Japan |
| Japanese Red Cross Koga Hospital | Koga | Ibaraki | 306-0014 | Japan |
| Mito Kyodo General Hospital | Mito | Ibaraki | 310-0015 | Japan |
| Tokiwa Clinic | Totte | Ibaraki | 302-0011 | Japan |
| Tsuchiura Beryl Clinic | Tsuchiura | Ibaraki | 300-0062 | Japan |
| Kikuchi Medical Clinic | Tsukuba | Ibaraki | 305-0861 | Japan |
| Japanese Red Cross Ishinomaki Hospital | Ishinomaki | Miyagi | 986-8522 | Japan |
| Iida Hospital | Iida | Nagano | 395-8505 | Japan |
| Toyonaka Keijinkai Clinic | Toyonaka | Osaka | 560-0004 | Japan |
| Kodaira Kitaguchi Clinic | Kodaira | Tokyo | 187-0001 | Japan |
| Medical corporation association Shunshin-kai Inage hospital | Chiba | 263-0043 | Japan |
| Fukuoka Renal Clinic | Fukuoka | 810-0004 | Japan |
| Ohmiya Chuo General Hospital | Saitama | 331-8711 | Japan |
| Yamagata Tokushukai Hospital | Yamagata | 990-0834 | Japan |
| D014570 |
| Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |