Rheumatoid Arthritis (RA)UPHOLDNCT04497597
A Study of Oral Upadacitinib Tablets to Assess Treatment Patterns, Achievement of Treatment Targets and Maintenance of Response in Adult Participants With Moderate to Severe Rheumatoid Arthritis
An observational study of Rheumatoid Arthritis (RA), run by AbbVie at 263 sites in 19 countries.
Trial summary
Rheumatoid Arthritis (RA) is an inflammatory disease of the joints causing pain, stiffness, swelling and loss of joint function. Despite the range of treatment options for RA steadily increasing, many patients remain sub-optimally managed, with sustained clinical remission rarely achieved. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Rheumatoid Arthritis (RA)
- How many people
- 1,532 participants
- Where
- 263 sitesin 19 countries
- Study dates
- 16 Oct 2020to 15 May 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adults receiving Upadacitinib according to the product prescribing information, for moderate to severe active Rheumatoid Arthritis (RA).
Who may be able to join
- Confirmed diagnosis of moderate to severe active Rheumatoid Arthritis (RA).
- Physician decision on patient treatment with upadacitinib must have been reached prior to and independently of recruitment in the study.
- Upadacitinib prescribed in accordance to the applicable approved label and local regulatory and reimbursement policies.
- French Participants Only: Taking oral glucocorticoids ≥5 mg/day of prednisone or equivalent for at least 3 months prior to study start.
Who cannot join
- Prior treatment with Upadacitinib.
Trial locations and contacts
263 sites in 19 countries.
263 sites in 19 countries
France73 sites
CH du Pays d'AIX /ID# 229561
Aix-en-Provence, 13616
Cabinet medical /ID# 225366
Aix-les-Bains, Savoie, 73100
Cabinet medical /ID# 224850
Albi, Tarn, 81000
CHU Amiens-Picardie Site Sud /ID# 222444
Amiens, Somme, 80054
Centre Hospitalier d'Angouleme /ID# 226064
Angoulême, Charente, 16959
Cabinet Novel d'Annecy /ID# 232310
Annecy, 74000
Centre Hospitalier d'Arras /ID# 223172
Arras, 62022
CHU de Besancon - Jean Minjoz /ID# 222463
Besançon, Doubs, 25030
Hopital Avicenne - APHP /ID# 224248
Bobigny, Île-de-France Region, 93000
CHU Bordeaux - Hopital Pellegrin /ID# 224837
Bordeaux, Gironde, 33076
Centre Hospitalier de Boulogne Sur Mer /ID# 222991
Boulogne-sur-Mer, 62200
Hopital de la Cavale Blanche /ID# 222462
Brest, Finistere, 29200
cabinet liberal- Dr CORNILLE /ID# 227869
Caen, Calvados, 14000
Centre Hospitalier Jean Rougie /ID# 224242
Cahors, 46005
Infirmerie Protestante /ID# 222438
Caluire-et-Cuire, Rhone, 69300
CH Cannes - les Broussailles /ID# 226160
Cannes, Alpes-Maritimes, 06414
CHRU Tours - Hopital Trousseau /ID# 222445
Chambray-lès-Tours, 37170
Centre Hospitalier de CHOLET /ID# 222455
Cholet, 49300
Hia Percy /Id# 225642
Clamart, 92190
CHU Clermont Ferrand - Hopital Gabriel Montpied /ID# 223801
Clermont-Ferrand, 63000
Cabinet liberal - Compiegne - Dr Banse /ID# 227099
Compiègne, Oise, 60200
C. H. Sud Francilien /ID# 222446
Corbeil-Essonnes, 91106
CHU Dijon /ID# 223799
Dijon, Cote-d Or, 21000
Cabinet medical /ID# 225142
Haguenau, 67500
CHD Vendée- La Roche-sur-Yon - Les Oudairies /ID# 229086
La Roche-sur-Yon, Vendee, 85000
CH La Rochelle - Hopital Saint Louis /ID# 224240
La Rochelle, 17019
CHU Grenoble - Hopital Michallon /ID# 223211
La Tronche, Isere, 38700
Centre Hospitalier de Laon /ID# 224857
Laon, Aisne, 02001
CH Emile Roux Le Puy en Velay /ID# 223688
Le Puy-en-Velay, 43000
Cabinet médical /ID# 225000
Les Abrets En Dauphine, Isere, 38490
CHU Lille - Hôpital Roger Salengro /ID# 223170
Lille, 59037
CHU Limoges - Dupuytren 1 /ID# 222457
Limoges, Franche-Comte, 87042
Clinique de la Sauvegarde /ID# 223424
Lyon, 69009
Hopital Saint Joseph /ID# 227221
Marseille, Bouches-du-Rhone, 13008
Cabinet de rhumatologie /ID# 227740
Mennecy, Essonne, 91540
CH Princesse Grace /ID# 222451
Monaco, 98000
Ch Montauban /Id# 231854
Montauban, 82000
ELSAN - Clinique du Pont de Chaume /ID# 224898
Montauban, 82000
Clinique Beau Soleil /ID# 224238
Montpellier, Herault, 34070
CHU Montpellier - Hopital Saint Eloi /ID# 222452
Montpellier, Herault, 34295
CHU Montpellier - Hopital Saint Eloi /ID# 223394
Montpellier, Herault, 34295
CH des Pays de Morlaix /ID# 223795
Morlaix, Finistere, 29600
Polyclinique saint Odilon /ID# 225576
Moulins, Allier, 03000
Ch Mulhouse /Id# 223442
Mulhouse, 68100
CHU de Nantes, Hotel Dieu -HME /ID# 225787
Nantes, Pays de la Loire Region, 44000
CHU Nice -Hopital Pasteur /ID# 222460
Nice, Provence-Alpes-Côte d'Azur Region, 06002
CH Georges Renon /ID# 225197
Niort, Deux-Sevres, 79028
Centre Hospitalier Régional d'Orléans - Hôpital de la Source /ID# 223591
Orléans, 45067
Hopitaux Universitaires Paris Centre-Hopital Cochin /ID# 222986
Paris, Paris, 75679
AP-HP - Hopital Saint-Antoine /ID# 222441
Paris, 75012
Hopital Pitie Salpetriere /ID# 222443
Paris, 75013
Cabinet medical /ID# 224855
Paris, 75014
Centre de Soins Osteoarticulaires Ambulatoires /ID# 224737
Paris, 75015
AP-HP - Hopital Bichat - Claude-Bernard /ID# 222449
Paris, 75018
GH Diaconesses Croix Saint-Simon /ID# 229126
Paris, 75020
Cabinet libéral du Dr PAUPIERE /ID# 238723
Péronne, Somme, 80200
HCL - Hopital Lyon Sud /ID# 222447
Pierre-Bénite, Rhone, 69495
Cabinet médical /ID# 225321
Reims, Marne, 51100
CHU de Rennes - Hospital Sud /ID# 222458
Rennes, 35203
CH Roanne /ID# 224729
Roanne, Pays de la Loire Region, 42300
CH Roubaix - Hopital Victor Provo /ID# 225032
Roubaix, Hauts-de-France, 59100
Clinique Saint-Hilaire /ID# 223833
Rouen, 76000
Hôpital Charles-Nicolle /ID# 223589
Rouen, 76000
Hôpital d'instruction des armées Bégin /ID# 222440
Saint-Mandé, 94163
Cabinet Rhumatologie St Michel Sur Orge /ID# 225176
Saint-Michel-sur-Orge, Essonne, 91240
CH Saint Nazaire /ID# 225750
Saint-Nazaire, 44600
Centre Hospitalier Universitaire de Saint Étienne - Hôpital Nord /ID# 222456
Saint-Priest-en-Jarez, 42270
Cabinet rhumatologie Dr NECTOUX /ID# 225828
Sainte-Maxime, 83120
CHU Strasbourg - Hopital de Hautepierre /ID# 222450
Strasbourg, Bas-Rhin, 67200
Groupe Médical Spécialisé - Le Premium /ID# 223719
Strasbourg, 67000
CH Bigorre - Site de la Gespe /ID# 225141
Tarbes, Hautes-Pyrenees, 65013
Cabinet de Rhumatologie Poincare /ID# 224755
Thionville, Moselle, 57100
CHU Toulouse - Hopital Purpan /ID# 223150
Toulouse, Haute-Garonne, 31059
Italy29 sites
Azienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo /ID# 228889
Alessandria, 15100
ASL 3 Genovese - Ospedale la Colletta /ID# 228892
Arenzano, Genova, 16011
Azienda Ospedaliera Universitaria Consorziale Policlinico /ID# 228580
Bari, 70124
Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII (Presidio Papa Giovanni /ID# 228967
Bergamo, 24127
ASST Spedali civili di Brescia /ID# 228970
Brescia, 25123
Ospedale Ss. Annunziata /ID# 228809
Chieti, 66100
Azienda Ospedaliero Universitaria di Ferrara - Ospedale Sant'Anna /ID# 228788
Cona, Ferrara, 44124
Ospedale San Raffaele IRCCS /ID# 229059
Milan, Milano, 20132
ASST Grande Ospedale Metropolitano Niguarda /ID# 228807
Milan, Milano, 20162
ASST Gaetano Pini/Presidio Ospedaliero Pini /ID# 228556
Milan, 20122
Azienda Ospedaliero-Universitaria di Modena /ID# 228554
Modena, 41124
AOU Universita degli Studi della Campania Luigi Vanvitelli /ID# 229057
Naples, 80138
Ospedale San Giovanni Bosco /ID# 228552
Naples, 80144
Azienda Ospedaliera Civico Di Cristina Benfratelli- P.O. Civico /ID# 228912
Palermo, 90127
Azienda Ospedaliera Universitaria Paolo Giaccone /ID# 228160
Palermo, 90127
Fondazione IRCCS Policlinico /ID# 227937
Pavia, 27100
Azienda Ospedaliero Universitaria Pisana /ID# 228550
Pisa, 56126
Azienda Ospedaliera Regionale San Carlo /ID# 228648
Potenza, 85100
Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Universita Cattolica /ID# 229061
Rome, Lazio, 00168
Fondazione Policlinico Universitario Campus Bio-Medico di Roma /ID# 229063
Rome, Roma, 00128
Sapienza University /ID# 228014
Rome, Roma, 00161
Azienda Ospedaliero-Universitaria Sant'Andrea /ID# 227942
Rome, 00189
Istituto Clinico Humanitas /ID# 227943
Rozzano, Milano, 20089
Azienda Ospedaliera Universitaria "San Giovanni di Dio e Ruggi d'Aragona /ID# 229065
Salerno, 84131
Azienda Ospedaliero-Universitaria Senese-Ospedale Santa Maria delle Scotte /ID# 227938
Siena, 53100
Azienda Ospedaliero Universitaria Ospedali Riuniti Do Ancona /ID# 229440
Torette, Ancona, 60020
Ospedale Mauriziano di Torino /ID# 228888
Turin, Torino, 10128
Azienda Ospedaliera Universitaria Friuli Centrale/Presidio Ospedaliero Universit /ID# 228551
Udine, 33100
Azienda Ospedaliera Universitaria di Verona/Ospedale Borgo Trento /ID# 228553
Verona, 37126
Spain28 sites
Complejo Hospitalario Universitario A Coruña /ID# 231818
A Coruña, A Coruna, 15006
Hospital Universitario Torrecardenas /ID# 241931
Almería, 04009
Hospital Perpetuo Socorro /ID# 231827
Badajoz, 06010
Hospital Parc de Salut del Mar /ID# 240000
Barcelona, 08003
Hospital Santa Creu i Sant Pau /ID# 231821
Barcelona, 08041
Hospital General de Granollers /ID# 238778
Barcelona, 08042
Hospital Ernest Lluch Martin /ID# 238779
Calatayud, Zaragoza, 50299
Hospital General Universitario Santa Lucia /ID# 238780
Cartagena, Murcia, 30202
Hospital Universitario Reina Sofia /ID# 231843
Córdoba, Cordoba, 14004
Hospital Clinico Universitario Virgen de la Arrixaca /ID# 231847
El Palmar, Murcia, 30120
Hospital Universitario de Getafe /ID# 231825
Getafe, Madrid, 28905
Hospital Universitario Virgen de las Nieves /ID# 231841
Granada, 18014
Hospital Juan Ramon Jimenez /ID# 231840
Huelva, 21005
Hospital Universitario de Jaen /ID# 231842
Jaén, 23007
Hospital Universitario de Jerez de la Frontera /ID# 231844
Jerez de la Frontera, Cadiz, 11407
Hospital Rafael Mendez /ID# 231846
Lorca, Murcia, 30817
Hospital Universitario Ramon y Cajal /ID# 241901
Madrid, 28034
Hospital Universitario Virgen de la Victoria /ID# 240150
Málaga, 29010
Hospital de Mérida /ID# 231826
Mérida, Badajoz, 06800
Hospital Virgen del Puerto /ID# 240149
Plasencia, Caceres, 10600
Hospital Universitario Canarias /ID# 231848
San Cristóbal de La Laguna, Santa Cruz De Tenerife, 38320
Hospital Universitario Virgen Macarena /ID# 231837
Seville, 41009
Hospital Universitario Virgen del Rocio /ID# 231836
Seville, 41013
Hospital Universitario Virgen de Valme /ID# 231838
Seville, 41014
Hospital Universitari Mútua Terrassa /ID# 231822
Terrassa, Barcelona, 08221
Hospital Xeral Cies (CHUVI) /ID# 231819
Vigo, Pontevedra, 36204
Hospital de Viladecans /ID# 231823
Viladecans, Barcelona, 08840
Hospital Royo Villanova /ID# 231824
Zaragoza, 50015
Germany19 sites
ACURA Rheumazentrum Baden-Bade /ID# 225225
Baden-Baden, 76530
Rheumapraxis Prof Dr Karin Manger /ID# 224086
Bamberg, 96047
Praxis fuer Rheumatologie und Innere Medizin /ID# 225222
Berlin, 12163
Eisterhues, Braunschweig, DE /ID# 225186
Braunschweig, 38100
Rheumatologie in Veedel /ID# 224999
Cologne, 50825
Dres. Karger/Baerlecken /ID# 224809
Cologne, 50996
Praxis Dilltal /ID# 226925
Ehringshausen, 35630
MVZ Ambulantes Rheumazentrum Erfurt /ID# 224812
Erfurt, 99096
Helios Fachklinik Vogelsang-Gommern /ID# 222949
Gommern, 39245
Asklepios MVZ Nord SH GmbH /ID# 225048
Hamburg, 20097
Heilig, Heidelberg, DE /ID# 225223
Heidelberg, 69120
Praxis internistische Rheumatologie /ID# 239226
Leipzig, 04129
Dres. Teipel/Toussaint/Saech /ID# 226923
Leverkusen, 51373
Aurich & Sieburg, Magdeburg /ID# 230701
Magdeburg, 39104
Die Fachaerzte im Rottal - Nephrologie, Rheumatologie /ID# 223866
Pfarrkirchen, 84347
MVZ für Rheumatologie Dr. M. Welcker /ID# 226926
Planegg, 82152
Rheumatologische-Immunologische Praxis Templin /ID# 226924
Templin, Brandenburg, 17268
Krankenhaus der Barmherzigen Brüder Trier /ID# 226927
Trier, 54292
Praxis Dr. Haas /ID# 225187
Tübingen, Baden-Wurttemberg, 72072
Russia18 sites
District clinical hospital /ID# 227662
Khanty-Mansyisk, 628011
Moscow Regional Research and Clinical Institute n.a. Vladimirskiy (MONIKI) /ID# 224852
Moscow, Moscow Oblast, 129110
City Clinical Hospital #52 /ID# 242947
Moscow, 123182
Omsk Regional Clinic Hospital /ID# 232029
Omsk, 644111
Orenburg State Medical University /ID# 243615
Orenburg, 460000
Republican hospital named after V.A. Baranov /ID# 227661
Petrozavodsk, 185019
Nort-Western State Medical University n.a. Mechnikov /ID# 223419
Saint Petersburg, Sankt-Peterburg, 193015
Clinical Rheumatologic Hospital No 25 /ID# 242475
Saint Petersburg, 190068
Military Medical Academy n.a. Kirov /ID# 242351
Saint Petersburg, 194044
Samara Regional Clinical Hospital n.a. V. D. Seredavin /ID# 227852
Samara, Samara Oblast, 443095
Clinic of Samara State Medical University /ID# 241168
Samara, 443079
Budgetary Institution of the Khanty-Mansiysk Autonomous Okrug-Yugra Surgut Dist /ID# 243313
Surgut, 628400
LLC MC RevmaMed /ID# 239162
Syktyvkar, Komi, 167031
Nebbiolo Clinical Research Center /ID# 224900
Tomsk, 634009
GBUZ TO Regional Clinical Hospital No. 1 /ID# 241113
Tyumen, Tyumen Oblast, 625032
Ulyanovsk Regional Clinical Hospital /ID# 239164
Ulyanovsk, 432017
Voronezh State Medical Univers /ID# 224854
Voronezh, 394036
Yaroslavl State Medicat University /ID# 224851
Yaroslavl, 150000
Belgium14 sites
Algemeen Stedelijk Ziekenhuis /ID# 224121
Aalst, Oost-Vlaanderen, 9300
Onze Lieve Vrouw Hospital /ID# 223042
Aalst, 9300
AZ Sint-Jan Brugge /ID# 223713
Bruges, 8000
AZ Sint Lucas /ID# 223093
Bruges, 8310
CHU Saint Pierre /ID# 223041
Brussels, Brussels Capital, 1000
Rhumaconsult SPRL /ID# 221825
Charleroi, Hainaut, 6000
Reumacentrum /ID# 222799
Genk, 3600
ReumaClinic /ID# 221353
Genk, 3600
Maertens, Gistel, BE /ID# 221823
Gistel, 8470
Duplicate_CHU UCL Namur - site Godinne /ID# 222797
Godinne, Namur, 5530
Reuma Instituut Hasselt /ID# 221822
Hasselt, Limburg, 3500
CHU de Liege /ID# 222201
Liège, 4000
AZ Alma Campus Sijsele /ID# 222214
Sijsele, 8340
Private practice Sint-Niklaas /ID# 224123
Sint-Niklaas, Oost-Vlaanderen, 9100
Greece13 sites
University General Hospital of Alexandroupolis /ID# 224880
Alexandroupoli, Evros, 68100
251 Airforce General Hospital /ID# 225065
Athens, Attica, 11525
General Hospital of Athens Gennimatas /ID# 225064
Athens, Attica, 11527
General Hospital of Athens Ippokratio /ID# 224164
Athens, Attica, 11527
University General Hospital Attikon /ID# 224136
Athens, Attica, 12462
General Hospital Asklepieio Voulas /ID# 224131
Athens, Attica, 16673
Naval Hospital of Athens /ID# 224135
Athens, 11521
University General Hospital of Heraklion PA.G.N.I /ID# 224133
Heraklion, Crete, 71500
Olympion General Clinic /ID# 224130
Pátrai, Achaia, 25443
General Hospital of Patras Agios Andreas /ID# 224132
Pátrai, 26335
Bioclinic Thessaloniki /ID# 224879
Thessaloniki, 54622
General Hospital of Thessaloniki Hippokrateio /ID# 229965
Thessaloniki, 54642
Euromedica General Clinic /ID# 224134
Thessaloniki, 54645
Argentina9 sites
DOM Centro de Reumatologia /ID# 222194
Buenos Aires, 1111
Organizacion Medica de Investigacion (OMI) /ID# 222187
Ciudad Autonoma de Buenos Aire, Buenos Aires F.D., 1015
CIER Centro de Investigaciones en Enfermedades Reumaticas /ID# 231769
Ciudad Autonoma de Buenos Aire, Buenos Aires F.D., 1055
Instituto Medico Strusberg /ID# 222189
Córdoba, 5000
Hospital Italiano La Plata /ID# 222190
La Plata, Buenos Aires, 1902
CER Instituto Medico /ID# 222193
Quilmes, Buenos Aires, 1878
Instituto CAICI S.R.L /ID# 222191
Rosario, Santa Fe Province, 2000
CIMER Centro Integral de Medicina Respiratoria /ID# 222188
San Miguel de Tucumán, Tucumán Province, 4000
Instituto de Cardiologia /ID# 226634
Santiago del Estero, 4200
Israel9 sites
HaEmek Medical Center /ID# 222138
Afula, H_efa, 1834111
Hillel Yaffe Medical Center /ID# 222170
Hadera, H_efa, 38100
Rambam Health Care Campus /ID# 222118
Haifa, H_efa, 3109601
The Lady Davis Carmel Medical Center /ID# 223851
Haifa, H_efa, 34362
Rabin Medical Center /ID# 222694
Haifa, 4941492
Meir Medical Center /ID# 222116
Kfar Saba, Central District, 4428164
Galilee Medical Center /ID# 222113
Nahariya, Northern District, 2210001
The Chaim Sheba Medical Center /ID# 222034
Ramat Gan, Tel Aviv, 5265601
Tel Aviv Sourasky Medical Center /ID# 222117
Tel Aviv, Tel Aviv, 6423906
Mexico9 sites
Centro Integral en Reumatologia S.A de C.V /ID# 224363
Guadalajara, Jalisco, 44160
Clinica de Investigacion en Reumatologia y Obesidad S.C. /ID# 224361
Guadalajara, Jalisco, 44650
Private Office Dr. Orozco /ID# 243257
Guadalajara, Jalisco, 44650
Centro de Estudios de Investigación Básica y Clínica, S.C. /ID# 224364
Guadalajara, Jalisco, 44690
RM Pharma Specialists S.A de C.V. /ID# 224359
Mexico City, Mexico City, 03100
CINTRE, Centro de Investigación y Tratamiento Reumatológico SC /ID# 240836
Mexico City, Mexico City, 11850
Centro Especializado en Diabetes, Obesidad y Prevencion de Enfermedades Cardiova /ID# 224360
Mexico City, 11650
Consultorio Medico Privado - Miryam Eguia Bernal /Id# 243255
Monterrey, Nuevo León, 64000
Consultorio Privado Jorge Rojas Serrano /Id# 243258
Puebla City, 72550
Switzerland7 sites
Kantonsspital Aarau AG /ID# 222354
Aarau, Canton of Aargau, 5001
Universitätsspital Basel /ID# 224160
Basel Town, Canton of Basel-City, 4031
Inselspital, Universitaetsspital Bern /ID# 224951
Bern, 3010
HFR Fribourg - Hôpital cantonal /ID# 224163
Fribourg, 1708
CHUV, Centre hospitalier universitaire vaudois /ID# 224161
Lausanne, Canton of Vaud, 1011
Kantonsspital St. Gallen /ID# 224158
Sankt Gallen, Canton of St. Gallen, 9007
Rheumatologisches Versorgungszentrum Weinfelden /ID# 222346
Weinfelden, Thurgau, 8570
Austria6 sites
Dr. Georg Kurtz /ID# 225477
Gleisdorf, Styria, 8200
Ordination Dr. Leeb /ID# 224293
Hollabrunn, Lower Austria, 2020
Klinikum Klagenfurt am Wörthersee /ID# 239628
Klagenfurt, Carinthia, 9020
Dr. Maya Thun /ID# 224299
Vienna, State of Vienna, 1010
Ordination Doz. Grisar /ID# 224298
Vienna, State of Vienna, 1090
Rheuma-Zentrum Wien-Oberlaa GmbH /ID# 227853
Vienna, State of Vienna, 1100
Taiwan6 sites
Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 241052
Kaohsiung City, 807
China Medical University Hospital /ID# 241051
Taichung, 40447
Chi-Mei Medical Center /ID# 241745
Tainan, 71004
Tri-Service General Hospital /ID# 241746
Taipei, 11490
National Taiwan University Hospital /ID# 241050
Taipei City, Taipei, 100
Linkou Chang Gung Memorial Hospital /ID# 241053
Taoyuan City, 333
Australia5 sites
Private Practice - Scott Walter Graf /ID# 223958
Adelaide, South Australia, 5000
Genesis Research Services /ID# 224060
Broadmeadow, New South Wales, 2292
Emeritus Research /ID# 223883
Camberwell, Victoria, 3124
Joint West Rheumatology /ID# 223886
Murdoch, Western Australia, 6150
BJC Health /ID# 223884
Parramatta, New South Wales, 2150
Saudi Arabia5 sites
Saudi German Hospital Jeddah /ID# 243234
Jeddah, 22236
King Abdulaziz University Hospital /ID# 222724
Jeddah, 22252
International Medical Center /ID# 243235
Jeddah, 22382
Saudi German Hospital /ID# 224137
Mushait, 61961
King Fahad Medical City /ID# 222917
Riyadh, 11525
Ireland4 sites
St James Hospital /ID# 224201
Dublin, Dublin, D08 NHY1
Hermitage Medical Clinic /ID# 239556
Dublin, Dublin, D20 W722
St Vincent's University Hospital /ID# 224200
Elm Park, Dublin, D04 T6F4
Tallaght University Hospital /ID# 231260
Tallaght, Dublin, D24 NR0A
United Arab Emirates4 sites
Cleveland Clinic Abu Dhabi /ID# 223176
Abu Dhabi
Integrated Rheumatology and Arthritis Center /ID# 223177
Dubai, 334224
Departnent of Medicine-Rheumatology Al Baraha Hospital and Al Qasmi Hospital Min /ID# 223178
Dubai
Drt Sulaiman Al Habib Hospital /ID# 226575
Dubai
Kuwait3 sites
Mubarak Hospital /ID# 224139
Hawalli, 46300
Ameeri Hospital /ID# 224140
Kuwait City, 35002
KOC Hospital /ID# 224138
Kuwait City, 60000
Uruguay2 sites
Asociacion Española /ID# 222009
Montevideo, 11200
Medica Uruguaya /ID# 222008
Montevideo, 11600
About this study
Official title: Upadacitinib Treatment Patterns, Achievement of Treatment Targets and Maintenance of Response in Moderate to Severe Rheumatoid Arthritis Patients in Real-World Practice (UPHOLD)
Rheumatoid Arthritis (RA) is an inflammatory disease of the joints causing pain, stiffness, swelling and loss of joint function. Despite the range of treatment options for RA steadily increasing, many patients remain sub-optimally managed, with sustained clinical remission rarely achieved. This study will assess the treatment patterns, achievement of treatment targets and maintenance of response.
Upadacitinib is a drug approved for the treatment of moderately to severely active rheumatoid arthritis. Adult participants with moderate to severe RA who have been prescribed upadacitinib by their physicians will be enrolled. Approximately, 1660 participants will be enrolled this study, worldwide.
Read more
Participants will not receive Upadacitinib as part of this study, but will be followed for response to treatment for up to 24 months.
There may be higher burden for participants in this trial compared to their standard of care. Participants will attend regular visits, every 3 months, during the course of the study at a hospital or clinic and will be asked to provide additional information by questionnaire at each visit.
- Conditions
- Rheumatoid Arthritis (RA)
- Keywords
- Rheumatoid Arthritis, Upadacitinib, RINVOQ
- Medical subject headings
- Arthritis, Rheumatoid
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Participants receiving Upadacitinib | Participants receiving Upadacitinib for moderate to severe rheumatoid arthritis (RA). |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants Who Achieve Remission
Remission is defined as Disease Activity Score at 28 joints (DAS28) C-reactive Protein (CRP)<2.6.
Measured: At Month 6
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission
Remission is defined as DAS28-CRP<2.6. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: At Month 12
Secondary outcomes (23)
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission
Remission is defined as DAS28-CRP<2.6. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: At Month 24
Percentage of Participants Who Achieve Low Disease Activity (LDA) at 6 months that maintain LDA
LDA is defined as DAS28-CRP≤3.2. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: Through Month 24
Percentage of Participants Who Achieve Remission at 3 Months and Maintain Remission
Remission is defined as DAS28-CRP<2.6. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: Through Month 24
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission Grouped by Glucocorticoid Dose
Remission is defined as DAS28-CRP<2.6. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: At Month 12
Percentage of Participants Who Achieve LDA at 3 months that maintain LDA Grouped by Glucocorticoid Dose
LDA is defined as DAS28-CRP≤3.2. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
Measured: Through Month 6
Percentage of Participants in LDA that Achieve Glucocorticoid Dose <5 mg/Day Per Visit
LDA is defined as DAS28-CRP<3.2.
Measured: Through Month 24
Percentage of Participants in Remission that Achieve Glucocorticoid Dose <5 mg/Day Per Visit
Remission is defined as DAS28-CRP<2.6.
Measured: Through Month 24
Percentage of Participants Who Achieved a Glucocorticoid Dose <5 mg/Day Without Conventional Synthetic Disease Modifying Anti Rheumatic Drug (csDMARD) Intensification
Percentage of participants who achieved a glucocorticoid dose <5 mg/day without csDMARD intensification.
Measured: At Month 6
Percentage of Participants Who Initiated Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) That Moved to Monotherapy (+/- Glucocorticoids)
Percentage of participants who initiated Upadacitinib as combination therapy (csDMARD +/- Glucocorticoids) that moved to monotherapy (+/- glucocorticoids).
Measured: Through Week 24
Of the Participants Initiating Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) and Achieve Remission at 6 months, the Percentage of Participants that Maintain Remission Grouped by Maintenance of Combination Therapy Strategy
Remission is defined as DAS28-CRP<2.6.
Measured: Through Month 24
Of the Participants Initiating Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) and Achieve LDA at 6 months, the Percentage of Participants that Maintain LDA Grouped by Maintenance of Combination Therapy Strategy
LDA is defined as DAS28-CRP<3.2.
Measured: Through Month 24
Of the Participants Initiating Upadacitinib as Monotherapy Therapy (+/- Glucocorticoids) and Achieve Remission at 6 months, the Percentage of Participants that Maintain Remission Grouped by Maintenance of Monotherapy
Remission is defined as DAS28-CRP<2.6.
Measured: Through Month 24
Of the Participants Initiating Upadacitinib as Monotherapy Therapy (+/- Glucocorticoids) and Achieve LDA at 6 months, the Percentage of Participants that Maintain LDA Grouped by Maintenance of Monotherapy
LDA is defined as DAS28-CRP<3.2.
Measured: Through Month 24
Percentage of Participants Who Do Not Achieve Remission at Any Point in the Study
Remission is defined as DAS28-CRP<2.6.
Measured: Through Month 24
Time to the Discontinuation of Upadacitinib
Time to the discontinuation of Upadacitinib.
Measured: Through Month 24
Time to First Treatment Adjustment
Treatment Adjustment is defined as treatment escalation/de-escalation/ addition/withdrawal.
Measured: Baseline (Month 0) Through Month 24
Percentage of Participants Achieving LDA Grouped by Therapy Strategy
LDA is defined as DAS28-CRP<3.2, Simplified Disease Activity Index (SDAI) ≤11 and Clinical Disease Activity Index (CDAI) ≤10.
Measured: Through Month 24
Percentage of Participants Achieving Remission Grouped by Therapy Strategy
Remission is defined as DAS28-CRP<2.6, SDAI≤3.3 and CDAI ≤2.8.
Measured: Through Month 24
Change in Medication Burden Treatment Burden Questionnaire (TBQ) in Participants, Grouped by Therapy Strategy
The TBQ is composed of 13 items rated on a Likert scale ranging from 0 (not a problem), to 10 (big problem). scores can be summed into a global score, ranging from 0 to 130.
Measured: Through Week 24
Change in Physical Function Health Assessment Questionnaire - Disability Index (HAQ-DI) in Participants, Grouped by Therapy Strategy
HAQ is a widely accepted, validated, rheumatology specific instrument to assess physical function in Rheumatoid Arthritis. It consists of 20 questions, covering eight types of activities. For each question, scores range from 0 to 3 (0 = without any difficulty; 1 = with some difficulty; 2 = with much difficulty or with assistance; 3 = unable to do). HAQ Disability Index (HAQ-DI) score is the average of the highest score in each of the eight categories.
Measured: Baseline (Month 0) Through Month 24
Change in Pain Visual Analogue Scale (VAS) in participants, Grouped by Therapy Strategy
A VAS is used to assess worst joint pain in the past 7 days.
Measured: Baseline (Month 0) Through Month 24
Change in Morning Stiffness in Participants, Grouped by Therapy Strategy
A numeric rating scale (NRS) is used to assess severity and length of morning stiffness in the past 7 days.
Measured: Baseline (Month 0) Through Month 24
Change in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F) in Participants, Grouped by Therapy Strategy
The FACIT Fatigue Scale is a short, 13-item, easy to administer tool that measures an individual's level of fatigue during their usual daily activities over the past week. The level of fatigue is measured on a four-point Likert scale (0 = not at all fatigued to 4 = very much fatigued).
Measured: Baseline (Month 0) Through Month 24
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Aug 2020
- Study start16 Oct 2020
- Primary completion15 May 2024
- Study completion15 May 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Rheumatoid Arthritis (RA)Studies of the same condition, open and under way.
- More trials run by AbbVieThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,532 participants (actual)
Sponsor and investigators
- Lead sponsor
- AbbVie
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- ABBVIE INC., Study director, AbbVie
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04497597
- Sponsor's protocol ID
- P20-095
- Acronym
- UPHOLD
- Status last verified
- Apr 2025
- First submitted
- 30 Jul 2020
- Last updated
- 13 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Baldi C, Celletti E, Bugatti S, Govoni M, Cazzato M, Picchianti Diamanti A, Fornaro M, Guggino G, Navarini L, D'Agostino MA, Quartuccio L, Ciccia F, Dagna L, Stobbione P, Triggiani M, Viapiana O, Giardina A, Moroncini G, Caporali R, Bazzani C, Tirri E, Lomater C, Di Fino S, Morello F, Selmi C. Achievement and Maintenance of Remission with Upadacitinib in Patients with Moderate-to-Severe Rheumatoid Arthritis in Italy: 1-Year Data from UPHOLD, a Prospective Real-World Observational Study. Rheumatol Ther. 2026 Jun;13(3):767-784. doi: 10.1007/s40744-026-00845-2. Epub 2026 Apr 12.
PubMed 41968259Ostor A, Feist E, Sidiropoulos P, Avouac J, Rebella M, Namas R, Buttgereit F, Conaghan PG, Romero AB, McDearmon-Blondell EL, Lagunes-Galindo I, Gao T, Kadakia A, Shaw T, Attar S. Achievement and Maintenance of Disease Targets with Upadacitinib in Rheumatoid Arthritis: 2-Year Outcomes from the UPHOLD Real-World Study. Rheumatol Ther. 2026 Jun;13(3):659-676. doi: 10.1007/s40744-026-00826-5. Epub 2026 Mar 19.
PubMed 41854829Hugle T, Prillwitz H, Scholz G, Kyburz D, Dudler J, Schmiedeberg K, Zanisi L, Harrer Kuster MD, Roulin PS, Rubbert-Roth A. Sleep improvement in patients with rheumatoid arthritis treated with upadacitinib in real-world practice: results from the SLEERA study. Arthritis Res Ther. 2026 Feb 27;28(1):80. doi: 10.1186/s13075-026-03766-1.
PubMed 41761286Ostor A, Feist E, Sidiropoulos P, Avouac J, Rebella M, Namas R, McDearmon-Blondell E, Gao T, Lagunes-Galindo I, Strengholt S, Zisman D, Attar S. Achievement of treatment targets and maintenance of response with upadacitinib in patients with moderate-to-severe rheumatoid arthritis in real-world practice: 1-year outcomes from the UPHOLD observational study. Arthritis Res Ther. 2025 Apr 10;27(1):84. doi: 10.1186/s13075-025-03528-5.
PubMed 40211417
Study at a glance
From the registry record, last updated by the sponsor on 13 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Upadacitinib Treatment Patterns, Achievement of Treatment Targets and Maintenance of Response in Moderate to Severe Rheumatoid Arthritis Patients in Real-World Practice (UPHOLD)
- ClinicalTrials.gov ID
- NCT04497597
- Acronym / sponsor ID
- UPHOLD / P20-095
- Conditions
- Rheumatoid Arthritis (RA)
- Keywords
- Rheumatoid Arthritis, Upadacitinib, RINVOQ
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,532 participants (actual)
- Lead sponsor
- AbbVieIndustry (pharma, biotech, devices)
- Study start
- 16 Oct 2020 (actual)
- Primary completion
- 15 May 2024 (actual)
- Study completion
- 15 May 2024 (actual)
- First posted
- 4 Aug 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Rheumatoid Arthritis (RA) is an inflammatory disease of the joints causing pain, stiffness, swelling and loss of joint function. Despite the range of treatment options for RA steadily increasing, many patients remain sub-optimally managed, with sustained clinical remission rarely achieved. This study will assess the treatment patterns, achievement of treatment targets and maintenance of response.
Upadacitinib is a drug approved for the treatment of moderately to severely active rheumatoid arthritis. Adult participants with moderate to severe RA who have been prescribed upadacitinib by their physicians will be enrolled. Approximately, 1660 participants will be enrolled this study, worldwide.
Participants will not receive Upadacitinib as part of this study, but will be followed for response to treatment for up to 24 months.
There may be higher burden for participants in this trial compared to their standard of care. Participants will attend regular visits, every 3 months, during the course of the study at a hospital or clinic and will be asked to provide additional information by questionnaire at each visit.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Participants receiving Upadacitinib | – | –Participants receiving Upadacitinib for moderate to severe rheumatoid arthritis (RA). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adults receiving Upadacitinib according to the product prescribing information, for moderate to severe active Rheumatoid Arthritis (RA).
Key inclusion criteria (4 listed)
- Confirmed diagnosis of moderate to severe active Rheumatoid Arthritis (RA).
- Physician decision on patient treatment with upadacitinib must have been reached prior to and independently of recruitment in the study.
- Upadacitinib prescribed in accordance to the applicable approved label and local regulatory and reimbursement policies.
- French Participants Only: Taking oral glucocorticoids ≥5 mg/day of prednisone or equivalent for at least 3 months prior to study start.
Key exclusion criteria (1 listed)
- Prior treatment with Upadacitinib.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Percentage of Participants Who Achieve Remission
Time frame: At Month 6
Remission is defined as Disease Activity Score at 28 joints (DAS28) C-reactive Protein (CRP)<2.6.
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission
Time frame: At Month 12
Remission is defined as DAS28-CRP<2.6. Maintaining remission is defined as no more than 0.6 point increase in DAS28-CRP.
23 secondary outcomes
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission
Time frame: At Month 24
Percentage of Participants Who Achieve Low Disease Activity (LDA) at 6 months that maintain LDA
Time frame: Through Month 24
Percentage of Participants Who Achieve Remission at 3 Months and Maintain Remission
Time frame: Through Month 24
Percentage of Participants Who Achieve Remission at 6 Months and Maintain Remission Grouped by Glucocorticoid Dose
Time frame: At Month 12
Percentage of Participants Who Achieve LDA at 3 months that maintain LDA Grouped by Glucocorticoid Dose
Time frame: Through Month 6
Percentage of Participants in LDA that Achieve Glucocorticoid Dose <5 mg/Day Per Visit
Time frame: Through Month 24
Percentage of Participants in Remission that Achieve Glucocorticoid Dose <5 mg/Day Per Visit
Time frame: Through Month 24
Percentage of Participants Who Achieved a Glucocorticoid Dose <5 mg/Day Without Conventional Synthetic Disease Modifying Anti Rheumatic Drug (csDMARD) Intensification
Time frame: At Month 6
Percentage of Participants Who Initiated Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) That Moved to Monotherapy (+/- Glucocorticoids)
Time frame: Through Week 24
Of the Participants Initiating Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) and Achieve Remission at 6 months, the Percentage of Participants that Maintain Remission Grouped by Maintenance of Combination Therapy Strategy
Time frame: Through Month 24
Of the Participants Initiating Upadacitinib as Combination Therapy (csDMARD +/- Glucocorticoids) and Achieve LDA at 6 months, the Percentage of Participants that Maintain LDA Grouped by Maintenance of Combination Therapy Strategy
Time frame: Through Month 24
Of the Participants Initiating Upadacitinib as Monotherapy Therapy (+/- Glucocorticoids) and Achieve Remission at 6 months, the Percentage of Participants that Maintain Remission Grouped by Maintenance of Monotherapy
Time frame: Through Month 24
Of the Participants Initiating Upadacitinib as Monotherapy Therapy (+/- Glucocorticoids) and Achieve LDA at 6 months, the Percentage of Participants that Maintain LDA Grouped by Maintenance of Monotherapy
Time frame: Through Month 24
Percentage of Participants Who Do Not Achieve Remission at Any Point in the Study
Time frame: Through Month 24
Time to the Discontinuation of Upadacitinib
Time frame: Through Month 24
Time to First Treatment Adjustment
Time frame: Baseline (Month 0) Through Month 24
Percentage of Participants Achieving LDA Grouped by Therapy Strategy
Time frame: Through Month 24
Percentage of Participants Achieving Remission Grouped by Therapy Strategy
Time frame: Through Month 24
Change in Medication Burden Treatment Burden Questionnaire (TBQ) in Participants, Grouped by Therapy Strategy
Time frame: Through Week 24
Change in Physical Function Health Assessment Questionnaire - Disability Index (HAQ-DI) in Participants, Grouped by Therapy Strategy
Time frame: Baseline (Month 0) Through Month 24
Change in Pain Visual Analogue Scale (VAS) in participants, Grouped by Therapy Strategy
Time frame: Baseline (Month 0) Through Month 24
Change in Morning Stiffness in Participants, Grouped by Therapy Strategy
Time frame: Baseline (Month 0) Through Month 24
Change in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F) in Participants, Grouped by Therapy Strategy
Time frame: Baseline (Month 0) Through Month 24
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Apr 2025.
- Derived from this study: PubMed 41968259Baldi C, Celletti E, Bugatti S, Govoni M, Cazzato M, Picchianti Diamanti A, Fornaro M, Guggino G, Navarini L, D'Agostino MA, Quartuccio L, Ciccia F, Dagna L, Stobbione P, Triggiani M, Viapiana O, Giardina A, Moroncini G, Caporali R, Bazzani C, Tirri E, Lomater C, Di Fino S, Morello F, Selmi C. Achievement and Maintenance of Remission with Upadacitinib in Patients with Moderate-to-Severe Rheumatoid Arthritis in Italy: 1-Year Data from UPHOLD, a Prospective Real-World Observational Study. Rheumatol Ther. 2026 Jun;13(3):767-784. doi: 10.1007/s40744-026-00845-2. Epub 2026 Apr 12.
- Derived from this study: PubMed 41854829Ostor A, Feist E, Sidiropoulos P, Avouac J, Rebella M, Namas R, Buttgereit F, Conaghan PG, Romero AB, McDearmon-Blondell EL, Lagunes-Galindo I, Gao T, Kadakia A, Shaw T, Attar S. Achievement and Maintenance of Disease Targets with Upadacitinib in Rheumatoid Arthritis: 2-Year Outcomes from the UPHOLD Real-World Study. Rheumatol Ther. 2026 Jun;13(3):659-676. doi: 10.1007/s40744-026-00826-5. Epub 2026 Mar 19.
- Derived from this study: PubMed 41761286Hugle T, Prillwitz H, Scholz G, Kyburz D, Dudler J, Schmiedeberg K, Zanisi L, Harrer Kuster MD, Roulin PS, Rubbert-Roth A. Sleep improvement in patients with rheumatoid arthritis treated with upadacitinib in real-world practice: results from the SLEERA study. Arthritis Res Ther. 2026 Feb 27;28(1):80. doi: 10.1186/s13075-026-03766-1.
- Derived from this study: PubMed 40211417Ostor A, Feist E, Sidiropoulos P, Avouac J, Rebella M, Namas R, McDearmon-Blondell E, Gao T, Lagunes-Galindo I, Strengholt S, Zisman D, Attar S. Achievement of treatment targets and maintenance of response with upadacitinib in patients with moderate-to-severe rheumatoid arthritis in real-world practice: 1-year outcomes from the UPHOLD observational study. Arthritis Res Ther. 2025 Apr 10;27(1):84. doi: 10.1186/s13075-025-03528-5.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
ABBVIE INC. study director
AbbVie
263 sites in 19 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Rheumatoid Arthritis (RA), run by AbbVie at 263 sites in 19 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 263 sites in France, Italy, Spain, Germany, Russia and 14 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants Who Achieve Remission (time frame: At Month 6). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04497597, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2025.