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| ID | Type | Description | Link |
|---|---|---|---|
| CA045-012 | Other Identifier | Bristol-Myers Squibb Protocol ID | |
| 2018-003636-79 | EudraCT Number |
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| Name | Class |
|---|---|
| Bristol-Myers Squibb | INDUSTRY |
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The main purpose of this study is to evaluate the anti-tumor activity of bempegaldesleukin (NKTR-214) in combination with nivolumab by assessing the objective response rate (ORR) in cisplatin ineligible, locally advanced or metastatic urothelial cancer patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Combination of bempegaldesleukin (NKTR-214) + nivolumab | Experimental | Participants will receive bempegaldesleukin (NKTR-214) in combination with nivolumab. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bempegaldesleukin | Biological | Specified dose on specified days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in patients whose tumors have low programmed cell death ligand 1 (PD-L1) expression. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. CR is defined as disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) had to have reduction in short axis to <10 mm. PR is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months |
| Measure | Description | Time Frame |
|---|---|---|
| Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in All Treated Patients | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in all treated patients. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. CR is defined as disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) had to have reduction in short axis to <10 mm. PR is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. |
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Key Inclusion Criteria:
Key Exclusion Criteria:
Additional protocol-defined inclusion/exclusion criteria applied
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| Name | Affiliation | Role |
|---|---|---|
| Study Director | Nektar Therapeutics | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| San Francisco VA Medical Center - NAVREF - PPDS | San Francisco | California | 94143 | United States | ||
| Innovative Clinical Research Institute, LLC |
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192 patients were enrolled. Two patients withdrew consent before treatment. Two patients received Gemcitabine + Carboplatin under protocol amendment 2.0. The noncomparative, reference chemotherapy arm of gemcitabine + carboplatin was subsequently eliminated in protocol amendment 3.0. These four patients were excluded from the analysis.
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| ID | Title | Description |
|---|---|---|
| FG000 | Combination of Bempegaldesleukin (NKTR-214) + Nivolumab | Participants received bempegaldesleukin (NKTR-214) at 0.006 mg/kg administered every 3 weeks (q3w) in combination with 360 mg nivolumab q3w. The Treated Population included 188 patients; from these, 123 had tumors with low PD-L1 expression, 59 had tumors with high PD-L1 expression, and 6 had unknown PD-L1 expression. |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | May 27, 2021 | Dec 16, 2022 |
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| Nivolumab | Biological | Specified dose on specified days |
|
|
| Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| Duration of Response (DOR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the effect of NKTR 214 in combination with nivolumab by assessing DOR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in all treated patients and patients whose tumors have low PD-L1 expression. DOR is defined for patients who have a confirmed Complete Response (CR) or Partial Response (PR) as the date from first documented CR or PR per RECIST 1.1 to the date of documentation of disease progression as assessed by BICR or death due to any cause, whichever is earlier. Patients who do not have disease progression or die will be censored on the date of their last evaluable tumor assessment. | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 by Investigator in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by Investigator Assessment in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| Duration of Response (DOR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 by Investigator in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the effect of NKTR 214 in combination with nivolumab by assessing DOR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by Investigator Assessment in all treated patients and patients whose tumors have low PD-L1 expression. DOR is defined for patients who have a confirmed Complete Response (CR) or Partial Response (PR) as the date from first documented CR or PR per RECIST 1.1 to the date of documentation of disease progression as assessed by BICR or death due to any cause, whichever is earlier. Patients who do not have disease progression or die will be censored on the date of their last evaluable tumor assessment. | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| Whittier |
| California |
| 90603 |
| United States |
| Rocky Mountain Cancer Centers | Aurora | Colorado | 80012 | United States |
| Winship Cancer Institute, Emory University | Atlanta | Georgia | 30322 | United States |
| Southeastern Regional Medical Center - CTCA - PPDS | Newnan | Georgia | 30265 | United States |
| Investigator Site - Peoria | Peoria | Illinois | 61615 | United States |
| Laura And Isaac Perlmutter Cancer Center | New York | New York | 10016 | United States |
| MD Anderson Cancer Center | Houston | Texas | 77030 | United States |
| Centro de Investigación ClÃnica - ClÃnica Viedma | Viedma | RÃo Negro Province | R8500ACE | Argentina |
| Instituto de Oncologia de Rosario | Rosario | Santa Fe Province | S2000DSK | Argentina |
| CAIPO Centro para la atención integral del paciente oncológico | San Miguel de Tucumán | Tucumán Province | 4000 | Argentina |
| Hospital Alemán | Buenos Aires | C1118AAT | Argentina |
| Instituto Médico Especializado Alexander Fleming | Buenos Aires | C1426ANZ | Argentina |
| Centro Médico Privado CEMAIC | Córdoba | X5000HHW | Argentina |
| Sanatorio Privado Duarte Quirós, de ClÃnica Colombo S.A. | Córdoba | X5002AOQ | Argentina |
| St Vincent's Hospital Sydney | Darlinghurst | New South Wales | 2010 | Australia |
| Tasman Health Care | Southport | Queensland | 4215 | Australia |
| Adelaide Cancer Centre | Kurralta Park | South Australia | 5037 | Australia |
| Monash Health, Monash Medical Centre | Bentleigh East | Victoria | 3165 | Australia |
| St John of God Murdoch Hospital | Nedlands | Western Australia | 6009 | Australia |
| Algemeen Ziekenhuis Klina | Brasschaat | Antwerpen | 2930 | Belgium |
| GasthuisZusters Antwerpen | Wilrijk | Antwerpen | 2610 | Belgium |
| AZ Groeninge | Kortrijk | 8500 | Belgium |
| University Health Network | Toronto | Ontario | M5G 2M9 | Canada |
| Helsingin Yliopistollinen Keskussairaala - PPDS | Helsinki | 00290 | Finland |
| Centre François Baclesse | Caen | Calvados | 14076 | France |
| Hôpital Privé TOULON/HYERES Sainte Marguerite | Hyères | 83400 | France |
| Centre Jean Bernard Clinique Victor Hugo | Le Mans | 72015 | France |
| Hôpital Européen Georges Pompidou | Paris | 75908 | France |
| Edog Ico - Ppds | Saint-Herblain | 44805 | France |
| Institut Gustave Roussy | Villejuif | 94805 | France |
| Studienpraxis Urologie | Nürtingen | Baden-Wurttemberg | 72622 | Germany |
| Kliniken Nordoberpfalz AG | Weiden | Bavaria | 92637 | Germany |
| Charité - Universitätsmedizin Berlin | Berlin | 10117 | Germany |
| Universitätsklinikum Carl Gustav Carus an der TU Dresden | Dresden | 01307 | Germany |
| Alexandra Hospital | Athens | Attica | 115 28 | Greece |
| Medical Center of Athens | Marousi | Attica | 151 25 | Greece |
| University General Hospital of Larissa | Larissa | 41110 | Greece |
| Euromedica - PPDS | Thessaloniki | 54645 | Greece |
| Shamir Medical Center Assaf Harofeh | Ẕerifin | Central District | 70300 | Israel |
| Rambam Medical Center - PPDS | Haifa | 31096 | Israel |
| Meir Medical Center | Kfar Saba | 44281 | Israel |
| Sheba Medical Center - PPDS | Ramat Gan | 52621 | Israel |
| Tel Aviv Sourasky Medical Center PPDS | Tel Aviv | 52620 | Israel |
| Istituto Scientifico Romagnolo Per Lo Studio E La Cura Dei Tumori IRST - PPDS | Meldola | Emilia-Romagna | 47014 | Italy |
| Centro Di Riferimento Oncologico | Aviano | Pordenone | 33081 | Italy |
| Istituto Nazionale Dei Tumori | Milan | 20133 | Italy |
| Health Pharma Professional Research S.A de C.V. | Mexico City | Mexico City | 03810 | Mexico |
| Phylasis Clinicas Research S. de R.L. de C.V. | Cuautitlán Izcalli | 54769 | Mexico |
| Het Nederlands Kanker Instituut Antoni Van Leeuwenhoek Ziekenhuis | Amsterdam | 1066 | Netherlands |
| Centro Hospitalar E Universitário de Coimbra EPE | Coimbra | 3000-075 | Portugal |
| Regional Clinical Oncology Hospital | Yaroslavl | Yaroslavl Oblast | 150040 | Russia |
| Federal State Institution Medical Radiology Research Center | Obninsk | 249036 | Russia |
| Clinical Oncology Dispensary | Omsk | 644013 | Russia |
| PMI Euromedservice | Pushkin | 196603 | Russia |
| Railway Clinical Hospital JSC RZhD | Saint Petersburg | 195271 | Russia |
| Hospital General Universitario de Elche | Elche | Alicante | 03203 | Spain |
| Hospital de La Santa Creu i Sant Pau | Barcelona | Catalonia | 08025 | Spain |
| Hospital Universitario Ramon y Cajal | Pozuelo de Alarcón | Madrid | 28223 | Spain |
| Hospital del Mar | Barcelona | 08003 | Spain |
| Hospital Universitario 12 de Octubre | Madrid | 28041 | Spain |
| Hospital Universitario HM Sanchinarro - CIOCC | Madrid | 28050 | Spain |
| Hospital Universitario Virgen del Rocio - PPDS | Seville | 41013 | Spain |
| Fundacion Instituto Valenciano de Oncologia | Valencia | 46009 | Spain |
| Ankara University Medical Faculty - PPDS | Ankara | 6100 | Turkey (Türkiye) |
| Izmir Medicalpark Hospital | Izmir | 35530 | Turkey (Türkiye) |
| Inonu University Faculty of Medicine Turgut Ozal Medical Center | Malatya | 44280 | Turkey (Türkiye) |
| Royal Marsden Hospital - Surrey | Sutton | Surrey | SM2 5PT | United Kingdom |
| Leicester Royal Infirmary | Leicester | LE1 5WW | United Kingdom |
| Barts Health NHS Trust | London | EC1A 7BE | United Kingdom |
| COMPLETED |
|
| NOT COMPLETED |
|
|
The analysis population consisted of 188 patients.
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| ID | Title | Description |
|---|---|---|
| BG000 | Combination of Bempegaldesleukin (NKTR-214) + Nivolumab | Participants received bempegaldesleukin (NKTR-214) at 0.006 mg/kg administered every 3 weeks (q3w) in combination with 360 mg nivolumab q3w. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| ||||||||||||||||||||||
| Age, Customized | Count of Participants | Participants |
| |||||||||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| |||||||||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| |||||||||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
| |||||||||||||||||||||||
| Region of Enrollment | Number | participants |
| |||||||||||||||||||||||
| ECOG Performance Status | Measure Description: Eastern Cooperative Oncology Group (ECOG) performance status: ECOG Performance Status of 0 = Able to carry out all normal activities without restriction ECOG Performance Status of 1 = Restricted in physically strenuous activity but ambulatory and able to carry out work of light or sedentary nature | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in patients whose tumors have low programmed cell death ligand 1 (PD-L1) expression. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. CR is defined as disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) had to have reduction in short axis to <10 mm. PR is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. | The primary endpoint of ORR per RECIST 1.1 by BICR was evaluated in the Treated PD-L1 Low Population (123 patients). The Treated Population included 188 patients who were enrolled and received at least one full (or partial dose) of NKTR-214 or nivolumab. PD-L1 Low: Patients in the Treated Population whose tumors had low PD-L1 expression (defined as Combined Positive Score [CPS] < 10). From the 188 patients, 123 had tumors with low PD-L1 expression. | Posted | Count of Participants | Participants | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months |
|
|
| ||||||||||||||||||||||||||
| Secondary | Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in All Treated Patients | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in all treated patients. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. CR is defined as disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) had to have reduction in short axis to <10 mm. PR is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. | The secondary endpoint of ORR per RECIST 1.1 by BICR was evaluated in the Treated Population (188 patients). | Posted | Count of Participants | Participants | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| ||||||||||||||||||||||||||||
| Secondary | Duration of Response (DOR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 Per Blinded Independent Central Review (BICR) in in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the effect of NKTR 214 in combination with nivolumab by assessing DOR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per blinded independent central review (BICR) in all treated patients and patients whose tumors have low PD-L1 expression. DOR is defined for patients who have a confirmed Complete Response (CR) or Partial Response (PR) as the date from first documented CR or PR per RECIST 1.1 to the date of documentation of disease progression as assessed by BICR or death due to any cause, whichever is earlier. Patients who do not have disease progression or die will be censored on the date of their last evaluable tumor assessment. | All Treated Population who had a confirmed Complete Response (CR) or Partial Response (PR) per RECIST 1.1. Treated PD-L1 Low: Patients in the Treated Population whose tumors had low PD-L1 expression (defined as Combined Positive Score [CPS] < 10). | Posted | Median | 95% Confidence Interval | Months | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| |||||||||||||||||||||||||||
| Secondary | Objective Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 by Investigator in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the anti-tumor activity of NKTR-214 in combination with nivolumab by assessing the ORR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by Investigator Assessment in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression. ORR was defined as the percentage of patients with confirmed objective response of Complete Response (CR) or Partial Response (PR) on or before the first progressive disease and any subsequent anticancer therapy. | The All Treated Population included 188 patients who were enrolled and received at least one full (or partial dose) of NKTR-214 or nivolumab. Treated PD-L1 Low: Patients in the Treated Population whose tumors had low PD-L1 expression (defined as Combined Positive Score [CPS] < 10). From the 188 patients, 123 had tumors with low PD-L1 expression. | Posted | Count of Participants | Participants | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
| ||||||||||||||||||||||||||||
| Secondary | Duration of Response (DOR) by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 by Investigator in All Treated Patients and Patients Whose Tumors Have Low Programmed Cell Death Ligand (PD-L1) Expression | To evaluate the effect of NKTR 214 in combination with nivolumab by assessing DOR by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by Investigator Assessment in all treated patients and patients whose tumors have low PD-L1 expression. DOR is defined for patients who have a confirmed Complete Response (CR) or Partial Response (PR) as the date from first documented CR or PR per RECIST 1.1 to the date of documentation of disease progression as assessed by BICR or death due to any cause, whichever is earlier. Patients who do not have disease progression or die will be censored on the date of their last evaluable tumor assessment. | All Treated Population who had a confirmed Complete Response (CR) or Partial Response (PR) per RECIST 1.1. Treated PD-L1 Low: Patients in the Treated Population whose tumors had low PD-L1 expression (defined as Combined Positive Score [CPS] < 10). | Posted | Median | 95% Confidence Interval | Months | Tumor assessments were performed at baseline and every 9 weeks from Cycle 1 Day 1 for the first 12 months, and then every 12 weeks as indicated in the Schedule of Events, up to approximately 27 months. |
|
AEs were reported from the time of first study drug(s) administration until 100 days after the last dose of all study drug(s), up to a maximum of approximately 27 months.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Combination of Bempegaldesleukin (NKTR-214) + Nivolumab | Participants will receive bempegaldesleukin (NKTR-214) in combination with nivolumab. Bempegaldesleukin: Specified dose on specified days Nivolumab: Specified dose on specified days | 127 | 188 | 98 | 188 | 185 | 188 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Urinary tract infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Acute kidney injury | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Haematuria | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pneumonia | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urosepsis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Corona virus infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Fatigue | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pain in extremity | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pulmonary embolism | Respiratory, thoracic and mediastinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urinary tract infection enterococcal | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hydronephrosis | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Nephritis | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| General physical health deterioration | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Atrial fibrillation | Cardiac disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cardiac failure | Cardiac disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Myocarditis | Cardiac disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Deep vein thrombosis | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypotension | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Peripheral ischaemia | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Dehydration | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cerebrovascular accident | Nervous system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Bacterial sepsis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Escherichia urinary tract infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Gastroenteritis viral | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Herpes zoster | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Lung infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Peritonitis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pharyngitis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pyelonephritis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pyelonephritis acute | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pyelonephritis chronic | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Renal abscess | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Sepsis | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Spinal cord infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Upper respiratory tract infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Vascular device infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Bladder neck obstruction | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Chronic kidney disease | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Kidney congestion | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Renal failure | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urinary retention | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urinary tract discomfort | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urinary tract obstruction | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Abdominal pain | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Diverticulum intestinal | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Ileus | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Inguinal hernia | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Intestinal obstruction | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Intestinal perforation | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Large intestinal obstruction | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Obstruction gastric | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pancreatitis | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Rectal haemorrhage | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Retroperitoneal haemorrhage | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Asthenia | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Sudden death | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Bone pain | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Musculoskeletal chest pain | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pathological fracture | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Polymyalgia rheumatica | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Acute myocardial infarction | Cardiac disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cardio-respiratory arrest | Cardiac disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Peripheral arterial occlusive disease | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Peripheral artery thrombosis | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Thrombophlebitis superficial | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Decreased appetite | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hyperglycaemia | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypervolaemia | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Type 2 diabetes mellitus | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Anaemia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Eosinophilia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Febrile neutropenia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Haemorrhagic anaemia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cerebral infarction | Nervous system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cerebral microembolism | Nervous system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Lung disorder | Respiratory, thoracic and mediastinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cervical vertebral fracture | Injury, poisoning and procedural complications | MedDRA (21.1) | Non-systematic Assessment |
| |
| Lumbar vertebral fracture | Injury, poisoning and procedural complications | MedDRA (21.1) | Non-systematic Assessment |
| |
| Procedural pain | Injury, poisoning and procedural complications | MedDRA (21.1) | Non-systematic Assessment |
| |
| Breast cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (21.1) | Non-systematic Assessment |
| |
| Malignant melanoma in situ | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pancreatic carcinoma metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cholecystitis | Hepatobiliary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hepatic failure | Hepatobiliary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Confusional state | Psychiatric disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Delirium | Psychiatric disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Female genital tract fistula | Reproductive system and breast disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Perineal pain | Reproductive system and breast disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Scrotal pain | Reproductive system and breast disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cutaneous vasculitis | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Stevens-Johnson syndrome | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypophysitis | Endocrine disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Drug hypersensitivity | Immune system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Device occlusion | Product Issues | MedDRA (21.1) | Non-systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Pyrexia | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Fatigue | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Decreased appetite | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Anaemia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Constipation | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pruritus | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pruritus generalised | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Urinary tract infection | Infections and infestations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Asthenia | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Oedema peripheral | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Haematuria | Renal and urinary disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypothyroidism | Endocrine disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Chills | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Eosinophilia | Blood and lymphatic system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Blood creatinine increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Influenza like illness | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Dizziness | Nervous system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypotension | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Rash | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Dyspnoea | Respiratory, thoracic and mediastinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Headache | Nervous system disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Rash maculo-papular | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hyperthyroidism | Endocrine disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Abdominal pain | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Rash generalised | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Gamma-glutamyltransferase increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Insomnia | Psychiatric disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Pain in extremity | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Weight decreased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Dry skin | Skin and subcutaneous tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Musculoskeletal pain | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hyponatraemia | Metabolism and nutrition disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Myalgia | Musculoskeletal and connective tissue disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Blood alkaline phosphatase increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Infusion related reaction | Injury, poisoning and procedural complications | MedDRA (21.1) | Non-systematic Assessment |
| |
| Dry mouth | Gastrointestinal disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Amylase increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Aspartate aminotransferase increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Hypertension | Vascular disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Face oedema | General disorders | MedDRA (21.1) | Non-systematic Assessment |
| |
| Alanine aminotransferase increased | Investigations | MedDRA (21.1) | Non-systematic Assessment |
| |
| Fall | Injury, poisoning and procedural complications | MedDRA (21.1) | Non-systematic Assessment |
|
There are restrictions to the PI's rights to discuss or publish trial results.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Study Director | Nektar Therapeutics | 855-482-8676 | StudyInquiry@nektar.com |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Feb 22, 2022 | Dec 16, 2022 | SAP_001.pdf |
Not provided
| ID | Term |
|---|---|
| D001749 | Urinary Bladder Neoplasms |
| D009362 | Neoplasm Metastasis |
| D002295 | Carcinoma, Transitional Cell |
| ID | Term |
|---|---|
| D014571 | Urologic Neoplasms |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D001745 | Urinary Bladder Diseases |
| D014570 | Urologic Diseases |
| D052801 | Male Urogenital Diseases |
| D009385 | Neoplastic Processes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
Not provided
Not provided
| ID | Term |
|---|---|
| C000611752 | bempegaldesleukin |
| D000077594 | Nivolumab |
| ID | Term |
|---|---|
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |
Not provided
Not provided
| Age 85 and Over |
|
| Unknown or Not Reported |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| United Kingdom |
|
| Portugal |
|
| Russia |
|
| Spain |
|
| Greece |
|
| Canada |
|
| Netherlands |
|
| Turkey |
|
| Belgium |
|
| Finland |
|
| Italy |
|
| Mexico |
|
| Israel |
|
| Australia |
|
| France |
|
| Germany |
|
| ECOG PS 2 |
|
|
|
| OG001 | Combination of Bempegaldesleukin (NKTR-214) + Nivolumab (PD-L1 Low Population) | Arm Group Description: Participants received bempegaldesleukin (NKTR-214) at 0.006 mg/kg administered every 3 weeks (q3w) in combination with 360 mg nivolumab q3w. |
|
|
| OG001 |
| Combination of Bempegaldesleukin (NKTR-214) + Nivolumab (PD-L1 Low Population) |
Arm Group Description: Participants received bempegaldesleukin (NKTR-214) at 0.006 mg/kg administered every 3 weeks (q3w) in combination with 360 mg nivolumab q3w. The PD-L1 Low Population included 123 patients. |
|
|
| OG001 |
| Combination of Bempegaldesleukin (NKTR-214) + Nivolumab (PD-L1 Low Population) |
Arm Group Description: Participants received bempegaldesleukin (NKTR-214) at 0.006 mg/kg administered every 3 weeks (q3w) in combination with 360 mg nivolumab q3w. |
|
|