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

Locations

  • Clinical Site 1001

    Boston, Massachusetts, 02215, United States

  • Clinical Site 1002

    Coral Gables, Florida, 33134, United States

  • Clinical Site 1003

    Portsmouth, New Hampshire, 03801, United States

  • Clinical Site 1004

    Philadelphia, Pennsylvania, 19103, United States

  • Clinical Site 1005

    Greenville, South Carolina, 29615, United States

  • Clinical Site 1007

    Fort Gratiot, Michigan, 48059, United States

  • Clinical Site 1008

    Savannah, Georgia, 31419, United States

  • Clinical Site 1009

    Sacramento, California, 95815, United States

  • Clinical Site 1010

    Cleveland, Ohio, 44106, United States

  • Clinical Site 1011

    Washington D.C., District of Columbia, 20010, United States

  • Clinical Site 1012

    Arlington, Texas, 76011, United States

  • Clinical Site 1013

    Tampa, Florida, 33613, United States

  • Clinical Site 1014

    Chicago, Illinois, 60640, United States

  • Clinical Site 1015

    Maitland, Florida, 32751, United States

  • Clinical Site 1016

    New York, New York, 10003, United States

  • Clinical Site 1017

    Dublin, Ohio, 43016, United States

  • Clinical Site 1018

    Johnston, Rhode Island, 02919, United States

  • Clinical Site 1019

    Pomona, California, 91767, United States

  • Clinical Site 1020

    Cincinnati, Ohio, 45219, United States

  • Clinical Site 1022

    Scottsdale, Arizona, 85260, United States

  • Clinical Site 1023

    The Bronx, New York, 10467, United States

  • Clinical Site 1024

    Murray, Kentucky, 42071, United States

  • Clinical Site 1025

    Providence, Rhode Island, 02903, United States

  • Clinical Site 1026

    Tucson, Arizona, 85704, United States

  • Clinical Site 1027

    North Miami Beach, Florida, 33162-4708, United States

  • Clinical Site 1028

    West Lafayette, Indiana, 47906, United States

  • Clinical Site 1029

    Boca Raton, Florida, 33486, United States

  • Clinical Site 1030

    Detroit, Michigan, 48201, United States

  • Clinical Site 1031

    Bowling Green, Kentucky, 42104, United States

  • Clinical Site 1032

    Northridge, California, 91325, United States

  • Clinical Site 1034

    Santa Monica, California, 90024, United States

  • Clinical Site 1035

    Pittsburgh, Pennsylvania, 15213, United States

  • Clinical Site 1036

    Brooklyn, New York, 10023, United States

  • Clinical Site 1037

    Scottsdale, Arizona, 85260, United States

  • Clinical Site 1041

    Oakland, Michigan, 48328, United States

  • Clinical Site 1042

    Boston, Massachusetts, 02115-5804, United States

  • Clinical Site 1101

    Saskatoon, Saskatchewan, S7K 2C1, Canada

  • Clinical Site 1103

    Barrie, Ontario, L4M 7G1, Canada

  • Clinical Site 1104

    Hamilton, Ontario, L8L 3C3, Canada

  • Clinical Site 1105

    Edmonton, Alberta, T5K 1X3, Canada

  • Clinical Site 1106

    Toronto, Ontario, M2N 3A6, Canada

  • Clinical Site 1107

    London, Ontario, N6A 2C2, Canada

  • Clinical Site 1108

    Edmonton, Alberta, T6W 4V4, Canada

  • Clinical Site 1110

    Montreal, Quebec, H1Y 3L1, Canada

  • Clinical Site 1111

    Québec, G1W 4R4, Canada

  • Clinical Site 1201

    Westmead, New South Wales, 2145, Australia

  • Clinical Site 1202

    Carlton, Victoria, 3053, Australia

  • Clinical Site 1203

    Darlinghurst, New South Wales, 2010, Australia

  • Clinical Site 1204

    Woolloongabba, Queensland, 4102, Australia

  • Clinical Site 1301

    Pleven, 5800, Bulgaria

  • Clinical Site 1302

    Lovech, 5500, Bulgaria

  • Clinical Site 1303

    Sofia, Sofia-Grad, 1463, Bulgaria

  • Clinical Site 1304

    Stara Zagora, 6003, Bulgaria

  • Clinical Site 1401

    Prague, Prague, 100 34, Czechia

  • Clinical Site 1402

    Prague, Prague, 150 06, Czechia

  • Clinical Site 1501

    Rouen, Seine-Maritime, 76031, France

  • Clinical Site 1502

    Lyon, Rhône, 69003, France

  • Clinical Site 1503

    Antony, Hauts-de-Seine, 92160, France

  • Clinical Site 1504

    Paris, Île-de-France Region, 75010, France

  • Clinical Site 1505

    Amiens, Picardie, 80054, France

  • Clinical Site 1601

    Bochum, North Rhine-Westphalia, 44791, Germany

  • Clinical Site 1602

    Münster, North Rhine-Westphalia, 48149, Germany

  • Clinical Site 1604

    Frankfurt am Main, Hesse, 60590, Germany

  • Clinical Site 1605

    Dresden, Saxony, 01307, Germany

  • Clinical Site 1606

    Erlangen, Bavaria, 91054, Germany

  • Clinical Site 1701

    Warszawa, Pomeranian Voivodeship, 02-507, Poland

  • Clinical Site 1702

    Wroclaw, Kuyavian-Pomeranian Voivodeship, 51-685, Poland

  • Clinical Site 1703

    Bialystok, Podlaskie Voivodeship, 15-453, Poland

  • Clinical Site 1704

    Ossy, Silesian Voivodeship, 42-624, Poland

  • Clinical Site 1705

    Warszawa, Pomeranian Voivodeship, 02-962, Poland

  • Clinical Site 1706

    Wroclaw, Lower Silesian Voivodeship, 50-566, Poland

  • Clinical Site 1801

    Manises, Valencia, 46940, Spain

  • Clinical Site 1802

    Granada, 18012, Spain

  • Clinical Site 1803

    Madrid, 28034, Spain

  • Clinical Site 1804

    Seville, 41009, Spain

  • Clinical Site 1901

    Torrette, Ancona, 60126, Italy

  • Clinical Site 1902

    Ferrara, 44124, Italy

  • Clinical Site 1903

    Rozzano, Milano, 20089, Italy

  • Clinical Site 1904

    Roma, 168, Italy

  • Clinical Site 1906

    Pisa, 56126, Italy

  • Clinical Site 1907

    Roma, 00144, Italy

  • Clinical Site 1908

    Milan, 20122, Italy

  • Clinical Site 2001

    Gaziantep, 27310, Turkey (Türkiye)

  • Clinical Site 2002

    Samsun, 55270, Turkey (Türkiye)

  • Clinical Site 2101

    Athens, Attica, 16121, Greece

  • Clinical Site 2102

    Efkarpia, Thessaloniki, 56429, Greece

  • Clinical Site 2103

    Athens, Attica, 124 62, Greece

  • Clinical Site 2201

    Trnava, Trnava Region, 917 75, Slovakia

  • Clinical Site 2202

    Svidník, Presov, 089 01, Slovakia

Conditions

Explore the condition pages connected to this study.