New drug trial offers hope for painful skin condition
NCT ID NCT06603077
Summary
This study is testing whether an investigational drug called AVTX-009 can reduce painful skin lesions in people with moderate to severe hidradenitis suppurativa (HS). About 250 participants will receive either AVTX-009 or a placebo for 16 weeks to see which is more effective at clearing lesions and reducing pain. The main goal is to see if the drug helps at least 75% of lesions clear up without causing significant side effects.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Clinical Site 1001
Boston, Massachusetts, 02215, United States
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Clinical Site 1002
Coral Gables, Florida, 33134, United States
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Clinical Site 1003
Portsmouth, New Hampshire, 03801, United States
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Clinical Site 1004
Philadelphia, Pennsylvania, 19103, United States
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Clinical Site 1005
Greenville, South Carolina, 29615, United States
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Clinical Site 1007
Fort Gratiot, Michigan, 48059, United States
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Clinical Site 1008
Savannah, Georgia, 31419, United States
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Clinical Site 1009
Sacramento, California, 95815, United States
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Clinical Site 1010
Cleveland, Ohio, 44106, United States
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Clinical Site 1011
Washington D.C., District of Columbia, 20010, United States
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Clinical Site 1012
Arlington, Texas, 76011, United States
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Clinical Site 1013
Tampa, Florida, 33613, United States
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Clinical Site 1014
Chicago, Illinois, 60640, United States
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Clinical Site 1015
Maitland, Florida, 32751, United States
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Clinical Site 1016
New York, New York, 10003, United States
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Clinical Site 1017
Dublin, Ohio, 43016, United States
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Clinical Site 1018
Johnston, Rhode Island, 02919, United States
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Clinical Site 1019
Pomona, California, 91767, United States
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Clinical Site 1020
Cincinnati, Ohio, 45219, United States
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Clinical Site 1022
Scottsdale, Arizona, 85260, United States
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Clinical Site 1023
The Bronx, New York, 10467, United States
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Clinical Site 1024
Murray, Kentucky, 42071, United States
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Clinical Site 1025
Providence, Rhode Island, 02903, United States
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Clinical Site 1026
Tucson, Arizona, 85704, United States
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Clinical Site 1027
North Miami Beach, Florida, 33162-4708, United States
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Clinical Site 1028
West Lafayette, Indiana, 47906, United States
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Clinical Site 1029
Boca Raton, Florida, 33486, United States
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Clinical Site 1030
Detroit, Michigan, 48201, United States
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Clinical Site 1031
Bowling Green, Kentucky, 42104, United States
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Clinical Site 1032
Northridge, California, 91325, United States
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Clinical Site 1034
Santa Monica, California, 90024, United States
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Clinical Site 1035
Pittsburgh, Pennsylvania, 15213, United States
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Clinical Site 1036
Brooklyn, New York, 10023, United States
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Clinical Site 1037
Scottsdale, Arizona, 85260, United States
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Clinical Site 1041
Oakland, Michigan, 48328, United States
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Clinical Site 1042
Boston, Massachusetts, 02115-5804, United States
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Clinical Site 1101
Saskatoon, Saskatchewan, S7K 2C1, Canada
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Clinical Site 1103
Barrie, Ontario, L4M 7G1, Canada
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Clinical Site 1104
Hamilton, Ontario, L8L 3C3, Canada
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Clinical Site 1105
Edmonton, Alberta, T5K 1X3, Canada
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Clinical Site 1106
Toronto, Ontario, M2N 3A6, Canada
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Clinical Site 1107
London, Ontario, N6A 2C2, Canada
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Clinical Site 1108
Edmonton, Alberta, T6W 4V4, Canada
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Clinical Site 1110
Montreal, Quebec, H1Y 3L1, Canada
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Clinical Site 1111
Québec, G1W 4R4, Canada
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Clinical Site 1201
Westmead, New South Wales, 2145, Australia
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Clinical Site 1202
Carlton, Victoria, 3053, Australia
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Clinical Site 1203
Darlinghurst, New South Wales, 2010, Australia
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Clinical Site 1204
Woolloongabba, Queensland, 4102, Australia
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Clinical Site 1301
Pleven, 5800, Bulgaria
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Clinical Site 1302
Lovech, 5500, Bulgaria
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Clinical Site 1303
Sofia, Sofia-Grad, 1463, Bulgaria
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Clinical Site 1304
Stara Zagora, 6003, Bulgaria
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Clinical Site 1401
Prague, Prague, 100 34, Czechia
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Clinical Site 1402
Prague, Prague, 150 06, Czechia
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Clinical Site 1501
Rouen, Seine-Maritime, 76031, France
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Clinical Site 1502
Lyon, Rhône, 69003, France
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Clinical Site 1503
Antony, Hauts-de-Seine, 92160, France
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Clinical Site 1504
Paris, Île-de-France Region, 75010, France
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Clinical Site 1505
Amiens, Picardie, 80054, France
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Clinical Site 1601
Bochum, North Rhine-Westphalia, 44791, Germany
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Clinical Site 1602
Münster, North Rhine-Westphalia, 48149, Germany
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Clinical Site 1604
Frankfurt am Main, Hesse, 60590, Germany
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Clinical Site 1605
Dresden, Saxony, 01307, Germany
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Clinical Site 1606
Erlangen, Bavaria, 91054, Germany
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Clinical Site 1701
Warszawa, Pomeranian Voivodeship, 02-507, Poland
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Clinical Site 1702
Wroclaw, Kuyavian-Pomeranian Voivodeship, 51-685, Poland
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Clinical Site 1703
Bialystok, Podlaskie Voivodeship, 15-453, Poland
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Clinical Site 1704
Ossy, Silesian Voivodeship, 42-624, Poland
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Clinical Site 1705
Warszawa, Pomeranian Voivodeship, 02-962, Poland
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Clinical Site 1706
Wroclaw, Lower Silesian Voivodeship, 50-566, Poland
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Clinical Site 1801
Manises, Valencia, 46940, Spain
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Clinical Site 1802
Granada, 18012, Spain
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Clinical Site 1803
Madrid, 28034, Spain
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Clinical Site 1804
Seville, 41009, Spain
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Clinical Site 1901
Torrette, Ancona, 60126, Italy
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Clinical Site 1902
Ferrara, 44124, Italy
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Clinical Site 1903
Rozzano, Milano, 20089, Italy
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Clinical Site 1904
Roma, 168, Italy
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Clinical Site 1906
Pisa, 56126, Italy
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Clinical Site 1907
Roma, 00144, Italy
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Clinical Site 1908
Milan, 20122, Italy
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Clinical Site 2001
Gaziantep, 27310, Turkey (Türkiye)
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Clinical Site 2002
Samsun, 55270, Turkey (Türkiye)
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Clinical Site 2101
Athens, Attica, 16121, Greece
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Clinical Site 2102
Efkarpia, Thessaloniki, 56429, Greece
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Clinical Site 2103
Athens, Attica, 124 62, Greece
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Clinical Site 2201
Trnava, Trnava Region, 917 75, Slovakia
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Clinical Site 2202
Svidník, Presov, 089 01, Slovakia
Conditions
Explore the condition pages connected to this study.