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| ID | Type | Description | Link |
|---|---|---|---|
| 2024-512016-22-00 | Registry Identifier | EU CT Number | |
| 2017-002259-26 | EudraCT Number |
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| Name | Class |
|---|---|
| Merck Sharp & Dohme LLC | INDUSTRY |
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The purpose of this study was to evaluate the efficacy and safety of pembrolizumab plus epacadostat compared to sunitinib or pazopanib in participants with locally advanced/metastatic renal cell carcinoma (mRCC) with a clear cell component who have not received prior systemic therapy for their mRCC.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pembrolizumab + Epacadostat | Experimental |
| |
| SoC (Sunitinib or Pazopanib) | Active Comparator | Standard of care (SoC) (sunitinib or pazopanib monotherapy). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pembrolizumab | Drug | Pembrolizumab 200 mg administered intravenously every 3 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Objective Response Rate (ORR) of Pembrolizumab + Epacadostat Versus Standard of Care (SOC) | ORR was defined as the percentage of participants who had complete response (CR) or partial response (PR) per RECIST v1.1 by investigator determination. | up to approximately 8 months |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and Tolerability of Pembrolizumab + Epacadostat Versus SOC as Measured by the Number of Participants Experiencing Adverse Events (AEs) | AE is defined as any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. | Data reported from start of study to data cutoff 28-Feb-2019, up to 15 months. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Mark Jones, MD | Incyte Corporation | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pinnacle Oncology Hematology | Scottsdale | Arizona | 85258 | United States | ||
| Scottsdale Healthcare |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39054430 | Derived | Lara PN Jr, Villanueva L, Ibanez C, Erman M, Lee JL, Heinrich D, Lipatov ON, Gedye C, Gokmen E, Acevedo A, Semenov A, Park SH, Gafanov RA, Kose F, Jones M, Du X, Munteanu M, Perini R, Choueiri TK, Motzer RJ. A randomized, open-label, phase 3 trial of pembrolizumab plus epacadostat versus sunitinib or pazopanib as first-line treatment for metastatic renal cell carcinoma (KEYNOTE-679/ECHO-302). BMC Cancer. 2024 Jul 25;23(Suppl 1):1253. doi: 10.1186/s12885-023-10971-7. |
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No new participants were enrolled after 02-MAY-2018. As the results did not meet statistical preplanned assumptions, the development of the combination therapy was stopped. At the time of discontinuation, participants were given the option to discontinue from the study or continue study treatment if they showed clinical benefit per investigators.
This study was conducted at 73 centers in 14 countries.
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| ID | Title | Description |
|---|---|---|
| FG000 | Pembrolizumab + Epacadostat | Pembrolizumab 200 mg administered intravenously every 3 weeks. Epacadostat 100 mg administered orally twice daily. |
| FG001 | SoC (Sunitinib or Pazopanib) |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jun 15, 2018 |
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| Epacadostat | Drug | Epacadostat 100 mg administered orally twice daily. |
|
|
| Sunitinib | Drug | Sunitinib 50 mg administered orally once daily; 4 weeks on, 2 weeks off for 6-wk cycle. |
|
|
| Pazopanib | Drug | Pazopanib 800 mg administered orally once daily. |
|
|
| Safety and Tolerability of Pembrolizumab + Epacadostat Versus SOC as Measured by the Number of Participants Discontinuing Study Drug Due to AEs | AE is defined as any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. | Data reported from start of study to data cutoff 28-Feb-2019, up to 15 months. |
| Scottsdale |
| Arizona |
| 85258 |
| United States |
| Arizona Oncology Associates PC- HOPE | Tucson | Arizona | 85711 | United States |
| Cedars-Sinai Medical Center | Los Angeles | California | 90048 | United States |
| UC Irvine Comprehensive Cancer Center/Chao Family Comprehensive Cancer Center | Orange | California | 92868 | United States |
| UC Davis Comprehensive Cancer Center | Sacramento | California | 95817 | United States |
| Woodlands Medical Specialists, PA | Pensacola | Florida | 32503 | United States |
| Northside Hospital | Atlanta | Georgia | 30342 | United States |
| Atlanta Cancer Care - Conyers | Conyers | Georgia | 30094 | United States |
| Northwest Georgia Oncology Centers Pc | Marietta | Georgia | 30060 | United States |
| Rush University Medical Center | Chicago | Illinois | 60612 | United States |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States |
| Dana Farber Cancer Institute | Boston | Massachusetts | 02215 | United States |
| Southeast Nebraska Hematology & Oncology Consultants, P.C. | Lincoln | Nebraska | 68510 | United States |
| New York Oncology Hematology P.C | Albany | New York | 12208 | United States |
| Memorial Sloan Kettering Cancer Center | New York | New York | 10065 | United States |
| Levine Cancer Institute | Charlotte | North Carolina | 28204 | United States |
| Willamette Valley Cancer Institute and Research Center | Eugene | Oregon | 97401 | United States |
| University of Tennessee Erlanger Oncology & Hematology | Chattanooga | Tennessee | 37403 | United States |
| The West Clinic, P.C. | Germantown | Tennessee | 38138 | United States |
| US Oncology and Research | The Woodlands | Texas | 77380 | United States |
| Utah Cancer Specialists | Salt Lake City | Utah | 84106 | United States |
| Huntsman Cancer Institute | Salt Lake City | Utah | 84112 | United States |
| Oncology & Hematology Associates of Southwest Virginia, Inc., DBA Blue Ridge Cancer Care | Roanoke | Virginia | 24014 | United States |
| Shenandoah Oncology, P.C. | Winchester | Virginia | 22601 | United States |
| Canberra Hospital | Garran | Australian Capital Territory | 2605 | Australia |
| Calvary Mater Newcastle | Waratah | New South Wales | 2298 | Australia |
| Westmead Hospital | Westmead | New South Wales | 2145 | Australia |
| Cabrini Health | Malvern | Victoria | 3144 | Australia |
| Fiona Stanley Hospital | Murdoch | 6150 | Australia |
| Centro de pesquisa Porto Alegre | Porto Alegre | Florianopolis | 90610-000 | Brazil |
| Fundacao Pio XII - Hospital de Cancer de Barretos | Barretos | São Paulo | 14784-400 | Brazil |
| Instituto do Cancer de Sao Paulo - ICESP | São Paulo | São Paulo | 01246-000 | Brazil |
| Hospital Sao Jose | São Paulo | São Paulo | 01321-001 | Brazil |
| Centro Avancado de Tratamento Oncologico - CENANTRON - | Belo Horizonte | 30130090 | Brazil |
| Hospital de Clinicas de Porto Alegre | Porto Alegre | 90035-903 | Brazil |
| Tom Baker Cancer Centre | Calgary | Alberta | T2N 4N2 | Canada |
| Kingston Health Sciences Centre - KGH Site | Kingston | Ontario | K7L 2V7 | Canada |
| Sunnybrook Health Sciences, Odette Cancer Centre | Toronto | Ontario | M4N 3M5 | Canada |
| Jewish General Hospital | Montreal | Quebec | H3T 1E2 | Canada |
| CHU de Quebec-Universite Laval-Hotel Dieu de Quebec | Québec | Quebec | G1R 2J6 | Canada |
| CIUSSS de la Mauricie-et-du-Centre-du-Quebec | Trois-Rivières | Quebec | G8Z 3R9 | Canada |
| Clinica Alemana de Osorno | Osorno | Los Lagos Region | 5311089 | Chile |
| Fundacion Arturo Lopez Perez FALP | Santiago | 7500921 | Chile |
| Pontificia Universidad Catolica de Chile | Santiago | 8320000 | Chile |
| Hospital Clinico Vina del Mar | Viña del Mar | 2520000 | Chile |
| Centre Antoine Lacassagne | Nice | Cedex 2 | 06189 | France |
| CHU Besancon - Hopital Jean Minjoz | Besançon | 25030 | France |
| Hopital Saint Andre | Bordeaux | 33075 | France |
| Centre Francois Baclesse | Caen | 14076 | France |
| Hopital Prive Toulon Hyeres Sainte Marguerite | Hyères | 83400 | France |
| Hopital Europeen Georges Pompidou | Paris | 75015 | France |
| Hospices Civils de Lyon Centre Hospitalier Lyon Sud | Pierre-Bénite | 69310 | France |
| Clinique Sainte Anne | Strasbourg | 67000 | France |
| CHU de Strasbourg - Nouvel Hopital Civil | Strasbourg | 67091 | France |
| Institut Gustave Roussy | Villejuif | 94805 | France |
| Helios Klinikum Berlin Buch | Berlin | 13125 | Germany |
| Universitaetsklinikum der Technischen Universitaet Dresden | Dresden | 01307 | Germany |
| Universitaetsklinikum Essen | Essen | 45147 | Germany |
| Universitaetsklinikum Frankfurt | Frankfurt am Main | 60590 | Germany |
| Medizinische Hochschule Hannover | Hanover | 30625 | Germany |
| Universitaetsklinikum Jena | Jena | 07747 | Germany |
| Universitaetsklinikum Magdeburg. Klinik fuer Urologie | Magdeburg | 39120 | Germany |
| Universitaetsklinikum Tuebingen | Tübingen | 72076 | Germany |
| Orszagos Onkologiai Intezet | Budapest | Pest County | 1122 | Hungary |
| Zala Megyei Szent Rafael Korhaz | Zalaegerszeg | Pozva | 8900 | Hungary |
| Somogy Megyei Kaposi Mor Oktato Korhaz | Kaposvár | 7400 | Hungary |
| Borsod-Abauj-Zemplen Megyei Korhaz es Egyetemi Oktato Korhaz | Miskolc | 3526 | Hungary |
| Jasz Nagykun Szolnok Megyei Hetenyi Geza Korhaz Rendelointezet | Szolnok | 5000 | Hungary |
| Markusovszky Egyetemi Oktatokorhaz | Szombathely | 9700 | Hungary |
| Adelaide & Meath Hospital | Dublin | 00024 | Ireland |
| University Hospital Waterford | Waterford | X91ER8E | Ireland |
| Medical Oncology Ospedale San Donato | Arezzo | 52100 | Italy |
| Azienda Ospedaliera-Spedali Civili | Brescia | 25123 | Italy |
| Fondazione IRCCS Istituto Nazionale dei Tumori | Milan | 20133 | Italy |
| A.O. Cardarelli | Naples | 80131 | Italy |
| Policlinico San Matteo | Pavia | 27100 | Italy |
| Azienda Ospedaliera San Camillo Forlanini | Roma | 00152 | Italy |
| Nagoya University Hospital | Nagoya | Aichi-ken | 466-8560 | Japan |
| National Cancer Center Hospital East | Kashiwa | Chiba | 277-8577 | Japan |
| Sapporo Medical University Hospital | Sapporo | Hokkaido | 060-8543 | Japan |
| Hokkaido University Hospital | Sapporo | Hokkaido | 060-8648 | Japan |
| Nara Medical University Hospital | Kashihara | Nara | 634-8522 | Japan |
| Kindai University Hospital | Sayama | Osaka | 589-8511 | Japan |
| Saitama Medical University International Medical Center | Hidaka | Saitama | 350-1298 | Japan |
| Yamaguchi University Hospital | Ube | Yamaguchi | 755-8505 | Japan |
| Akita University Hospital | Akita | 010-8543 | Japan |
| Kyushu University Hospital | Fukuoka | 812-8582 | Japan |
| Niigata University Medical & Dental Hospital | Niigata | 951-8520 | Japan |
| Toranomon Hospital | Tokyo | 105-8470 | Japan |
| Nippon Medical School Hospital | Tokyo | 113-8603 | Japan |
| Keio University Hospital | Tokyo | 160-8582 | Japan |
| Auckland City Hospital | Auckland | Grafton | 1023 | New Zealand |
| Helse Bergen HF Haukeland sykehus | Bergen | 5053 | Norway |
| Sykehuset Oestfold | Grålum | 1714 | Norway |
| Sorlandet sykehus HF | Kristiansand | 4615 | Norway |
| Akershus University Hospital | Lørenskog | 1478 | Norway |
| Oslo universitetssykehus | Oslo | 0450 | Norway |
| Universitetssykehuset i Nord Norge. Kreftavdelingen | Tromsø | 9019 | Norway |
| St Olavs Hospital | Trondheim | 7030 | Norway |
| Leningrad Regional Oncology Dispensary | Saint Petersburg | Leningrad Region, Vsevolozhsky District | 188663 | Russia |
| Ivanovo regional oncology dispensary | Ivanovo | 153040 | Russia |
| Russian Scientific Center of Roentgenoradiology | Moscow | 117997 | Russia |
| Central Clinical Hospital with outpatient Clinic | Moscow | 121359 | Russia |
| National Medical Research Radiology Centre | Moscow | 125284 | Russia |
| Republican Clinical Oncology Dispensary of Republic of Bashkortostan | Ufa | 450054 | Russia |
| Chonnam National University Hwasun Hospital | Hwasun | Jeollanam-do | 58128 | South Korea |
| Severance Hospital Yonsei University Health System | Seoul | 03722 | South Korea |
| Asan Medical Center | Seoul | 05505 | South Korea |
| Samsung Medical Center | Seoul | 06351 | South Korea |
| Hospital Parc Tauli | Sabadell | Barcelona | 08208 | Spain |
| Hospital del Mar | Barcelona | 08003 | Spain |
| Hospital Germans Trias i Pujol | Barcelona | 08916 | Spain |
| Hospital General Universitario Gregorio Maranon | Madrid | 28007 | Spain |
| Hospital Universitario HM Sanchinarro | Madrid | 28050 | Spain |
| Hospital Clinico Universitario de Santiago | Santiago de Compostela | 15706 | Spain |
| Instituto Valenciano de Oncologia | Valencia | 46009 | Spain |
| Chang Gung Med Foundation. Kaohsiung Branch | Kaohsiung City | 833 | Taiwan |
| China Medical University Hospital | Taichung | 40447 | Taiwan |
| National Cheng Kung University Hospital | Tainan | 70457 | Taiwan |
| National Taiwan University Hospital | Taipei | 10048 | Taiwan |
| Taipei Veterans General Hospital | Taipei | 112 | Taiwan |
| Baskent Universitesi Adana Dr. Turgut Noyan Uygulama ve Arastirma Merkezi | Adana | 01250 | Turkey (Türkiye) |
| Ankara Numune Education and Research Hospital | Ankara | 06100 | Turkey (Türkiye) |
| Hacettepe University Medical Faculty | Ankara | 06100 | Turkey (Türkiye) |
| Istanbul Universitesi Onkoloji Enstitusu | Istanbul | 34093 | Turkey (Türkiye) |
| Istanbul Medeniyet Universitesi Goztepe EAH | Istanbul | 34732 | Turkey (Türkiye) |
| Ege Universitesi Tıp Fakultesi | Izmir | 35040 | Turkey (Türkiye) |
| Namik Kemal Universitesi Tip Fakultesi | Tekirdağ | 59100 | Turkey (Türkiye) |
| MI Kryviy Rih Center of Dnipropetrovsk Regional Council | Kryvyi Rih | Dnipropetrovsk Oblast | 50048 | Ukraine |
| Dnipropetrovsk Regional Hospital n.a. I.I. Mechnikov | Dnipro | 49005 | Ukraine |
| Dnipropetrovsk City Multidiscipline Clinical Hosp. 4 of DRC | Dnipro | 49102 | Ukraine |
| MI Precarpathian Clinical Oncology Center | Ivano-Frankivsk | 76018 | Ukraine |
| RMI Sumy Regional Clinical Oncology Dispensary | Sumy | 40022 | Ukraine |
| The Royal Marsden NHS Foundation Trust. | Sutton | Surrey | SM2 5PT | United Kingdom |
| Western General Hospital | Edinburgh | EH4 2XU | United Kingdom |
| Beatson Institute of Cancer Research | Glasgow | G12 0YN | United Kingdom |
| Barts Health NHS Trust - St Bartholomew s Hospital | London | EC1A 7BE | United Kingdom |
| The Royal Marsden Foundation Trust | London | SW3 6JJ | United Kingdom |
| The Christie NHS Foundation Trust | Manchester | MB204BX | United Kingdom |
Standard of care (SoC) (sunitinib or pazopanib monotherapy). Sunitinib 50 mg administered orally once daily;4 weeks on, 2 weeks off for 6-wk cycle. Pazopanib 800 mg administered orally once daily.
| Intention-to-Treat (ITT) |
|
| All Subjects as Treated (ASaT) |
|
| COMPLETED |
|
| NOT COMPLETED |
|
|
The Intention-to-Treat (ITT) population consisted of all randomized participants.
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Pembrolizumab + Epacadostat | Pembrolizumab 200 mg administered intravenously every 3 weeks. Epacadostat 100 mg administered orally twice daily. |
| BG001 | SoC (Sunitinib or Pazopanib) | Standard of care (SoC) (sunitinib or pazopanib monotherapy). Sunitinib 50 mg administered orally once daily. Pazopanib 800 mg administered orally once daily. |
| BG002 | Total | Total of all reporting groups |
| 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 |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Race/Ethnicity, Customized | Count of Participants | Participants |
| ||||||||||||||||
| ECOG Performance Scale | The Eastern Cooperative Oncology Group (ECOG) scale describes a patient's level of functioning in terms of their ability to care for themselves, activity, and ability. The scale is from 0 to 5; 0 - Fully active; 1 - Restricted in physically strenuous activity but ambulatory; 2- Ambulatory and capable of all selfcare but unable to carry out any work activities; 3- Capable of only limited selfcare; confined to bed or chair more than 50% of waking hours; 4 - Completely disabled; 5 - Dead. | 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) of Pembrolizumab + Epacadostat Versus Standard of Care (SOC) | ORR was defined as the percentage of participants who had complete response (CR) or partial response (PR) per RECIST v1.1 by investigator determination. | The Intention-to-Treat (ITT) population consisted of all randomized participants | Posted | Number | 95% Confidence Interval | percentage of participants | up to approximately 8 months |
|
|
| |||||||||||||||||||||||||||||||||||
| Secondary | Safety and Tolerability of Pembrolizumab + Epacadostat Versus SOC as Measured by the Number of Participants Experiencing Adverse Events (AEs) | AE is defined as any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. | The All Subjects as Treated (ASaT) population was used for the safety analysis and consisted of all randomized participants who received at least 1 dose of study treatment. | Posted | Count of Participants | Participants | Data reported from start of study to data cutoff 28-Feb-2019, up to 15 months. |
|
| |||||||||||||||||||||||||||||||||||||
| Secondary | Safety and Tolerability of Pembrolizumab + Epacadostat Versus SOC as Measured by the Number of Participants Discontinuing Study Drug Due to AEs | AE is defined as any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. | The All Subjects as Treated (ASaT) population was used for the safety analysis and consisted of all randomized participants who received at least 1 dose of study treatment. | Posted | Count of Participants | Participants | Data reported from start of study to data cutoff 28-Feb-2019, up to 15 months. |
|
|
Non-serious adverse events were reported from start of study, up to 30 days after last dose and serious adverse events up to 90 days after last dose are included, up to 15 months
The All Participants as Treated (APaT) population was used for the safety analysis and consisted of all randomized participants who received at least 1 dose of study treatment. All-Cause Mortality was based on the ITT population and consisted of all randomized participants. MedDRA preferred terms "Neoplasm progression", "Malignant neoplasm progression" and "Disease progression" not related to the drug are excluded
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Pembrolizumab + Epacadostat | Pembrolizumab 200 mg administered intravenously every 3 weeks. Epacadostat 100 mg administered orally twice daily. | 8 | 64 | 18 | 64 | 61 | 64 |
| EG001 | SoC (Sunitinib or Pazopanib) | Standard of care (SoC) (sunitinib or pazopanib monotherapy). Sunitinib 50 mg administered orally once daily;4 weeks on, 2 weeks off for 6-wk cycle. Pazopanib 800 mg administered orally once daily. | 8 | 65 | 15 | 63 | 61 | 63 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Acute coronary syndrome | Cardiac disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Atrial fibrillation | Cardiac disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Cardiac failure | Cardiac disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pericardial effusion | Cardiac disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Adrenal insufficiency | Endocrine disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Gastrointestinal haemorrhage | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Large intestine perforation | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pancreatitis | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Small intestinal obstruction | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Asthenia | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Fatigue | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hepatobiliary disease | Hepatobiliary disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Bronchitis | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Gangrene | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Groin abscess | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Influenza | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Lung infection | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Pneumonia | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Sepsis | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Septic shock | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Upper respiratory tract infection | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Urinary tract infection | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Urosepsis | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Wound infection | Infections and infestations | MedDRA 21.1 | Systematic Assessment |
| |
| Humerus fracture | Injury, poisoning and procedural complications | MedDRA 21.1 | Systematic Assessment |
| |
| Platelet count decreased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Decreased appetite | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hypercalcaemia | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hyponatraemia | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Steroid diabetes | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Altered state of consciousness | Nervous system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Cerebral ischaemia | Nervous system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Seizure | Nervous system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Prostatomegaly | Reproductive system and breast disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Aspiration | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pleural effusion | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pulmonary embolism | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Rash generalised | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Deep vein thrombosis | Vascular disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Thrombosis | Vascular disorders | MedDRA 21.1 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Anaemia | Blood and lymphatic system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Thrombocytopenia | Blood and lymphatic system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hyperthyroidism | Endocrine disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hypothyroidism | Endocrine disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Abdominal distension | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Abdominal pain | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Abdominal pain upper | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Constipation | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Dry mouth | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Dyspepsia | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Stomatitis | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Asthenia | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Chest pain | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Fatigue | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Influenza like illness | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Oedema peripheral | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Alanine aminotransferase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Amylase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Aspartate aminotransferase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Blood alkaline phosphatase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Blood bilirubin increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Blood creatinine increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Blood lactate dehydrogenase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Lipase increased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Neutrophil count decreased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Platelet count decreased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Weight decreased | Investigations | MedDRA 21.1 | Systematic Assessment |
| |
| Decreased appetite | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hypercalcaemia | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hyponatraemia | Metabolism and nutrition disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Musculoskeletal pain | Musculoskeletal and connective tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Dysgeusia | Nervous system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Headache | Nervous system disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Insomnia | Psychiatric disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Haematuria | Renal and urinary disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Proteinuria | Renal and urinary disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Dysphonia | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Epistaxis | Respiratory, thoracic and mediastinal disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hair colour changes | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Palmar-plantar erythrodysaesthesia syndrome | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Pruritus | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Rash | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Rash maculo-papular | Skin and subcutaneous tissue disorders | MedDRA 21.1 | Systematic Assessment |
| |
| Hypertension | Vascular disorders | MedDRA 21.1 | Systematic Assessment |
|
Participants who continued treatment after development was stopped received pembrolizumab only or received standard of care (SoC) treatment (if originally randomized to the control arm). As the objective of the study was to assess the efficacy/safety of pembrolizumab in combination with epacadostat only versus SoC treatment, assessment of data collected beyond Week 12 (when participants started to receive monotherapy only) was not conducted per protocol to reduce participant/investigator burden.
Following the first publication, the Institution and/or Principal Investigator may publish data or results from the Study, provided, however, that the Institution and/or Principal Investigator submits the proposed publication to the Sponsor for review at least sixty (60) days prior to the date of the proposed publication. Sponsor may remove from the proposed publication any information that is considered confidential and/or proprietary other than Study data and results.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Study Director | Incyte Corporation | 855-463-3463 | medinfo@incyte.com |
| Jul 9, 2019 |
| Prot_SAP_000.pdf |
| ID | Term |
|---|---|
| D002292 | Carcinoma, Renal Cell |
| C565324 | Parkinson Disease 4, Autosomal Dominant Lewy Body |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D007680 | Kidney Neoplasms |
| D014571 | Urologic Neoplasms |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052801 | Male Urogenital Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| C582435 | pembrolizumab |
| C000613752 | epacadostat |
| D000077210 | Sunitinib |
| C516667 | pazopanib |
| ID | Term |
|---|---|
| D011758 | Pyrroles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D007211 | Indoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Asian |
|
| White |
|
| 1 |
|
| 2 |
|
| Objective Response (CR+PR) |
|
|
|
|
|