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Clinical Trial Details

Trial ID: L1622
Source ID: NCT01750190
Associated Drug: Roxadustat
Title: A Study of Roxadustat for the Treatment of Anemia in Participants With Chronic Kidney Disease and Not Receiving Dialysis
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT01750190/results
Conditions: CKD Anemia
Interventions: DRUG: Roxadustat|DRUG: Placebo
Outcome Measures: Primary: United States (US FDA) Submission: Mean Change From Baseline in Hb (g/dL) Over Weeks 28 to 52 Regardless of Rescue Therapy, The change in Hb from baseline to the average level during the evaluation period (defined as Week 28 until Week 52) is reported. Hb values under the influence of a rescue therapy were not censored. The intermittent missing hemoglobin data were imputed for each treatment relying on non-missing data from all participants within each treatment group using the Monte Carlo Markov Chain (MCMC) imputation model, Monotone missing data were imputed by regression from its own treatment group. Baseline Hb was defined as the mean of up to 4 last central laboratory values prior to the first dose of study drug., Baseline (Day 1, Week 0), Weeks 28 to 52|Ex-US Submission: Number (%) of Participants Who Achieved a Hb Response During the First 24-Weeks of Treatment Censoring for Rescue Therapy, The number of participants who achieved a Hb response at 2 consecutive visits at least 5 days apart during the first 24 weeks of treatment, without rescue therapy (that is, red blood cell \[RBC\] transfusion, erythropoiesis-stimulating agent \[ESA\], or intravenous \[IV\] iron) are reported. A Hb response is defined, using central laboratory values, as the following: * Hb ≥11 g/dL and Hb increase from baseline by ≥1 g/dL in participants with baseline Hb \>8 g/dL, or * An increase in Hb by ≥2 g/dL in participants with baseline Hb ≤8.0 g/dL, Baseline up to Week 24 | Secondary: Mean Change From Baseline in Hb Averaged Over Weeks 28 to 36 With Censoring for Rescue Therapy, For Ex-US submission only: Hb values under the influence of a rescue therapy were censored by mixed effect model of repeated measures (MMRM) for up to 6 weeks. Baseline Hb was defined as the mean of up to 4 last central laboratory values prior to the first dose of study drug., Baseline (Day 1, Week 0), Weeks 28 to 36|Mean Change From Baseline in Hb Averaged Over Weeks 28 to 52 Regardless of Rescue Therapy in Participants With Baseline C-Reactive Protein (CRP) >Upper Limit of Normal (ULN), Hb values under the influence of a rescue therapy were not censored in the analysis. The intermittent missing hemoglobin data were imputed for each treatment relying on non-missing data from all participants within each treatment group using the MCMC imputation model, Monotone missing data were imputed by regression from its own treatment group. Baseline Hb was defined as the mean of up to 4 last central laboratory values prior to the first dose of study treatment., Baseline (Day 1, Week 0), Weeks 28 to 52|Number (%) of Participants With Hb ≥10 g/dL Averaged Over Weeks 28 to 36 With Censoring for Rescue Therapy, Hb values under the influence of a rescue therapy were censored by Cochran-Mantel-Haenszel Test for up to 6 weeks. Responder was defined as: Hb ≥10.0 g/dL, which was based on central laboratory values., Weeks 28 to 36|Mean Change From Baseline in Low-Density Lipoprotein (LDL) Cholesterol Averaged Over Weeks 12 to 28, Baseline LDL cholesterol was defined as the last LDL cholesterol value prior to the first dose of study drug., Baseline (Day 1, Week 0), Weeks 12 to 28|Rate of Change in eGFR From Baseline up to 12 Months (Linear Random Coefficient Model With Observed Data), Progression of chronic kidney disease was measured by rate of change in eGFR over time adjusted by baseline eGFR, with censoring for chronic dialysis or kidney transplant, using random slope and intercept model. Least Square Mean of change from baseline at 1 year was derived based on a random slopes and intercepts model using all available eGFR values (1 baseline and all post-treatment values up to end of treatment period + 7 days or start of dialysis) adjusted on treatment, baseline Hb, baseline eGFR, geographical region, cardiovascular events history at Baseline (yes vs. no), time (continuous value), the interaction terms of baseline eGFR by time, baseline Hb by time, and treatment by time as fixed effects, with random effects of intercept and linear slope of time. All assessments collected after the start of stable dialysis or kidney transplant were excluded from the analysis., Baseline, Month 12|Number of Participants Who Received Blood/RBC Transfusion in the First 52 Weeks of Treatment, Participants with any use of blood/RBC transfusion were reported., Baseline up to Week 52|Number (%) of Participants Who Received Rescue Therapy in the First 24 Weeks and in the First 52 Weeks of Treatment, Rescue therapy included any use of RBC transfusion, ESA, or IV iron., Baseline (Day 1, Week 0) up to Week 24 and up to Week 52|Change From Baseline in Short Form 36 (SF-36) Version 2 Physical Functioning Subscore and Vitality Subscore at Weeks 12 to 28, The SF-36 V2 consists of 36 questions covering 8 health domains: physical functioning, bodily pain, role limitations due to physical problems, role limitations due to emotional problems, general health perceptions, mental health, social function, and vitality. The physical functioning subscore and vitality subscore are reported. The scores ranged from 0 (worst) to 100 (Best). A higher score indicates a general improvement of life quality or well-being. Baseline score was defined as the last physical functioning value or vitality value, as applicable, prior to the first dose of study drug., Baseline (Day 1, Week 0), Weeks 12 to 28|Number (%) of Participants Who Experienced Exacerbation of Hypertension, Exacerbation of hypertension was defined as an increase from baseline of ≥20 millimeter of mercury (mmHg) in systolic blood pressure (sBP) and sBP ≥170 mmHg or an increase from baseline of ≥15 mmHg in diastolic blood pressure (dBP) and dBP ≥110 mmHg., Baseline up to Week 52|Mean Change From Baseline in Mean Arterial Pressure (MAP) Averaged Over Weeks 20 to 28, Baseline MAP was defined as the last MAP value prior to the first dose of study drug., Baseline, Weeks 20 to 28
Sponsor/Collaborators: Sponsor: FibroGen | Collaborators: Astellas Pharma Europe B.V.|AstraZeneca
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 922
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2012-11-05
Completion Date: 2018-09-24
Results First Posted: 2021-10-01
Last Update Posted: 2021-10-01
Locations: Investigational Site, Huntsville, Alabama, 35801, United States|Investigational Site, Tempe, Arizona, 85284, United States|Investigational Site, Alhambra, California, 91801, United States|Investigational Site, Chula Vista, California, 91910, United States|Investigational Site, Inglewood, California, 90301, United States|Investigational Site, La Mesa, California, 91942, United States|Investigational Site, La Palma, California, 91324, United States|Investigational Site, Lynwood, California, 90262, United States|Investigational Site, Northridge, California, 91325, United States|Investigational Site, Paramount, California, 90723, United States|Investigational Site, Riverside, California, 92503, United States|Investigational Site, Roseville, California, 95661, United States|Investigational Site, San Dimas, California, 91773, United States|Investigational Site, Whittier, California, 90603, United States|Investigational Site, Coral Gables, Florida, 33134, United States|Investigational Site, Cutler Bay, Florida, 33157, United States|Investigational Site, Hialeah, Florida, 33016, United States|Investigational Site, Miami, Florida, 33015, United States|Investigational Site, Miami, Florida, 33122, United States|Investigational Site, Miami, Florida, 33135, United States|Investigational Site, Miami, Florida, 33150, United States|Investigational Site, Ocala, Florida, 34471, United States|Investigational Site, Pembroke Pines, Florida, 33028, United States|Investigational Site, South Miami, Florida, 33143, United States|Investigational Site, Winter Park, Florida, 32789, United States|Investigational Site, Augusta, Georgia, 30909, United States|Investigational Site, Caldwell, Idaho, 83605, United States|Investigational Site, Shreveport, Louisiana, 71101, United States|Investigational Site, Baltimore, Maryland, 21218, United States|Investigational Site, Boston, Massachusetts, 02215, United States|Investigational Site, Detroit, Michigan, 48202, United States|Investigational Site, Flint, Michigan, 48503, United States|Investigational Site, Flint, Michigan, 48532, United States|Investigational Site, Pontiac, Michigan, 48341, United States|Investigational Site, Roseville, Michigan, 48066, United States|Investigational Site, Saint Louis, Missouri, 63110, United States|Investigational Site, New Brunswick, New Jersey, 08903, United States|Investigational Site, Albuquerque, New Mexico, 87109, United States|Investigational Site, Bronx, New York, 10461, United States|Investigational Site, Mineola, New York, 11501, United States|Investigational Site, Asheville, North Carolina, 28801, United States|Investigational Site, Raleigh, North Carolina, 27609, United States|Investigational Site, Rocky Mount, North Carolina, 27804, United States|Investigational Site, Winston-Salem, North Carolina, 27103, United States|Investigational Site, Beaver, Pennsylvania, 15009, United States|Investigational Site, Orangeburg, South Carolina, 29118, United States|Investigational Site, Sumter, South Carolina, 29150, United States|Investigational Site, Nashville, Tennessee, 37232, United States|Investigational Site, Arlington, Texas, 76015, United States|Investigational Site, Corsicana, Texas, 75110, United States|Investigational Site, Dallas, Texas, 75246, United States|Investigational Site, Houston, Texas, 77030, United States|Investigational Site, San Antonio, Texas, 78229, United States|Investigational Site, Fairfax, Virginia, 22033, United States|Investigational Site, Morgantown, West Virginia, 26506, United States|Investigational Site, Ciudad Evita, Buenos Aires, B1178IFA, Argentina|Investigational Site, Moron, Buenos Aires, B1708DPN, Argentina|Investigational Site, González Catán, Provincia De Buenos Aires, B1759LTF, Argentina|Investigational Site, Junin, Provincia De Buenos Aires, B6000GMA, Argentina|Investigational Site, Pergamino, Provincia De Buenos Aires, B2700CPM, Argentina|Investigational Product, Villa Domínico, Provincia De Buenos Aires, B1874GBA, Argentina|Investigational Site, Ciudad de Cordoba, Provincia De Cordoba, X5002HWE, Argentina|Investigational Site, Buenos Aires, B1852FZD, Argentina|Investigational Site, Buenos Aires, C1425BPJ, Argentina|Investigational Site, Buenos Aires, C1429BWN, Argentina|Investigational Site, Cordoba, 5000, Argentina|Investigational Site, Cordoba, X5002AOQ, Argentina|Investigational site, Cordoba, X5016KET, Argentina|Investigational Site, Corrientes, 3400, Argentina|Investigational Site, Mendoza, 5500, Argentina|Investigational Site, Salta, A4402BGJ, Argentina|Investigational Site, Santa Fe, 3000, Argentina|Investigational Site, Liverpool, New South Wales, 2170, Australia|Investigational Site, Gosford, 2250, Australia|Investigational Site, Hobart, 7000, Australia|Investigational Site, Launceston, 7250, Australia|Investigational Site, Melbourne, 3004, Australia|Investigational Site, New Lambton Heights, 2305, Australia|Investigational Site, Randwick, 2031, Australia|Investigational Site, Temuco, Region De La Araucania, 4781151, Chile|Investigational Site, Santiago, Region Metropolitana, 8431657, Chile|Investigational Site, Barranquilla, Atlantico, Colombia|Investigational Site, Bogota, Cundinamarca, Colombia|Investigational Site, Hong Kong, Pokfulam, Hong Kong|Investigational Site, Chai Wan, Hong Kong|Investigational Site, Shatin, 852, Hong Kong|Investigational Site, Tai Po, Hong Kong|Investigational Site, Anyang-Si, Gyeonggi-Do, 431-796, Korea, Republic of|Investigational Site, Goyang-Si, Gyeonggi-Do, 410-719, Korea, Republic of|Investigational Site, Guri-Si, Gyeonggi-Do, 471-701, Korea, Republic of|Investigational Site, Seongnam-Si, Gyeonggi-Do, 463-712, Korea, Republic of|Investigational Site, Busan, 614-735, Korea, Republic of|Investigational Site, Seoul, 110-744, Korea, Republic of|Investigational Site, Seoul, 130-872, Korea, Republic of|Investigational Site, Seoul, 133-791, Korea, Republic of|Investigational Site, Seoul, 134-727, Korea, Republic of|Investigational Site, Seoul, 137-701, Korea, Republic of|Investigational Site, Seoul, 143-729, Korea, Republic of|Investigational Site, Seoul, Korea, Republic of|Investigational Site, Alor Setar, 05460, Malaysia|Investigational Site, Kajang, 43000, Malaysia|Investigational Site, Kuala Lumpur, 50586, Malaysia|Investigational Site, Kuala Lumpur, 59100, Malaysia|Investigational Site, Kuching, 93586, Malaysia|Investigational Site, Pulau Pinang, 10990, Malaysia|Investigational Site, Sungai Petani, 080000, Malaysia|Investigational Site, Taiping, 34000, Malaysia|Investigational Site, Mexico City, Distrito Federal, 06100, Mexico|Investigational Site, Guadalajara, Jalisco, 44280, Mexico|Investigational Site, Monterrey, Nuevo Leon, 64000, Mexico|Investigational Site, Merida, Yucatan, 97133, Mexico|Investigational Site, Aguascalientes, 20128, Mexico|Investigational Site, San Luis Potosi, 78240, Mexico|Investigational Site, Auckland, New Zealand|Investigational Site, Hamilton, 3240, New Zealand|Investigational Site, Tauranga, 3143, New Zealand|Investigational Site, Bellavista, Callao, Callao 2, Peru|Investigational Site, San Martin de Porres, Lima, Lima 31, Peru|Investigational site, Lima, Lima 13, Peru|Investigational Site, Lima, Lima 1, Peru|Investigational Site, Dasmarinas, Cavite, 4114, Philippines|Investigational Site, Davao City, Davao, 8000, Philippines|Investigational site, Pasig, Philippines|Investigational Site, Quezon City, 1100, Philippines|Investigational Site, Quezon City, 1102, Philippines|Investigational Site, Ponce, 00716, Puerto Rico|Investigational Site, San Juan, 00918, Puerto Rico|Investigational Site, Singapore, 119074, Singapore|Investigational Site, Singapore, 768828, Singapore|Investigational Site, Singapore, Singapore|Investigational Site, Changhua, 500, Taiwan|Investigational Site, Hualien City, 970, Taiwan|Investigational Site, Kaohsiung, 40705, Taiwan|Investigational Site, Kaohsiung, 81362, Taiwan|Investigational Site, Kaohsiung, 83301, Taiwan|Investigational Site, Taichung, 40705, Taiwan|Investigational Site, Taichung, 433, Taiwan|Investigational Site, Tainan City, 433, Taiwan|Investigational Site, Tainan, 704, Taiwan|Investigational Site, Taipei, 10002, Taiwan|Investigational Site, Taipei, 110, Taiwan|Investigational Site, Taipei, 11490, Taiwan|Investigational Site, Bangkok, 10330, Thailand|Investigational Site, Bangkok, 10400, Thailand|Investigational Site, Chiang Mai, 50200, Thailand
URL: https://clinicaltrials.gov/show/NCT01750190

Drug ID Drug Name Type DrugBank ID Targets Category Latest Progress