A Study of ANV419 Alone or in Combination With Approved Treatment in Patients With Cutaneous Melanoma (OMNIA-1).

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

December 16, 2022

Primary Completion Date

August 1, 2024

Study Completion Date

August 1, 2024

Conditions
Melanoma (Skin)Cutaneous MelanomaAdult DiseaseAdvanced Solid TumorMetastatic Melanoma
Interventions
DRUG

ANV419

ANV419 administered by intravenous (IV) infusion

Trial Locations (25)

10117

Charité - Universitätsmedizin Berlin, Berlin

22031

Virginia Cancer Specialists, Fairfax

28033

Centro Oncológico MD Anderson International España, Madrid

35294

University of Alabama at Birmingham, Birmingham

53100

Azienda Ospedaliero Universitaria Senese, Siena

55131

Universitätsmedizin der Johannes Gutenberg, Universität Mainz, Mainz

55905

Mayo Clinic, Rochester

59037

Centre Hospitalier Universitaire de Lille, Lille

60611

Northwestern University, Chicago

80045

University of Colorado Denver, Denver

80131

Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli

92093-0990

University of California San Diego, La Jolla

94143-1209

University of California San Francisco, San Francisco

21109A

HealthPartners Institute, Bloomington

07960

Atlantic Health System, Morristown

Unknown

Centre Georges François Leclerc, Dijon

CHU de Nantes, Nantes

AP-HP Hopital Saint-Louis, Paris

Gustave Roussy, Paris

CHU de Poitiers, Poitiers

"Istituto Romagnolo per lo Studio dei Tumori Dino Amadori", Meldola

Hospital Clinic de Barcelona, Barcelona

Hospital Universitario 12 de Octubre, Madrid

Clínica Universidad de Navarra, Pamplona

Universitary Hospital Virgen Macarena, Seville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Anaveon AG

INDUSTRY

NCT05578872 - A Study of ANV419 Alone or in Combination With Approved Treatment in Patients With Cutaneous Melanoma (OMNIA-1). | Biotech Hunter | Biotech Hunter