Phase
Condition
N/ATreatment
visugromab (CTL-002)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Main Inclusion Criteria:
Signed and dated informed consent, and able to comply with the study procedures andany locally required authorization.
Male or female aged ≥ 18 years.
Relapsed/refractory patients with histologically or cytologically confirmeddiagnosis of advanced-stage or recurrent cancer (Germany-specific: and haveexhausted all standard of care treatments or are not eligible for such treatments)
Progressed on/relapsed after at least one prior anti-PD-1/PD-L1 treatment
Biopsy-accessible tumor lesions and willing to undergo triple sequential tumorbiopsy (Part A) and dual biopsy (Part B, only for selected cohorts).
At least 1 radiologically measurable lesion per RECIST V1.1/imRECIST (Part B).
Eastern Cooperative Oncology Group (ECOG) performance status 0-1.
Life expectancy > 3 months as assessed by the Investigator.
Adequate organ function (bone marrow, hepatic, renal function and coagulation).
Exclusion
Main Exclusion Criteria:
Pregnant or breastfeeding.
Any tumor-directed therapy within 21 days before study treatment.
Treatment with investigational agent within 21 days before study treatment.
Radiotherapy within 14 days before study treatment.
Pre-existing arrhythmia, uncontrolled angina pectoris, uncontrolled heart failure (NYHA) Grade IV, any myocardial infarction/coronary event, CNS-ischemic event andany thromboembolic event at any time < 6 months prior to Screening or presence ofany uncontrolled heart failure NYHA Grade III or higher.
Left ventricular ejection fraction (LVEF) < 50% measured by echocardiogram or MUGA.
QTcF > 450 ms for men or > 470 ms for women.
Any active autoimmune requiring systemic immunosuppressive treatments. .
Any history of non-infectious pneumonitis < 6 months prior to Screening.
Any active inflammatory bowel disease such as Crohn's disease or ulcerative colitiswhich are generally excluded or active autoimmunthyroiditis present < 6 months priorto Screening.
History of CNS disease such as stroke, seizure, encephalitis, or multiple sclerosis (< 6 months prior to Screening).
Evidence for active infection with human immunodeficiency virus (HIV), hepatitis Bvirus (HBV), hepatitis C virus (HCV), tuberculosis (TB), or severe acute respiratorysyndrome coronavirus 2 (SARS-CoV-2).
Study Design
Connect with a study center
Universitätsklinikum Essen, Westdeutsches Tumorzentrum, Innere Klinik und Poliklinik
Essen, 45147
GermanySite Not Available
Universitätsklinikum Frankfurt, Medizinische Klinik I
Frankfurt am Main, 60590
GermanySite Not Available
Universitätsklinikum Würzburg, Comprehensive Cancer Center
Würzburg, 97078
GermanySite Not Available
Hospital Universitari Vall d'Hebron, Institute of Oncology
Barcelona, 08035
SpainSite Not Available
ICMDiM, Hospital Clinic
Barcelona, 08036
SpainSite Not Available
ICO Hospitalet, Hospital Duran i Reynals
Barcelona, 08908
SpainSite Not Available
Next Oncology, Phase I Unit. IOB - Hospital Quironsalud
Barcelona, 08023
SpainSite Not Available
Hospital Universitario 12 de Octubre
Madrid, 28041
SpainSite Not Available
START Madrid, Hospital Universitario HM Sanchinarro
Madrid, 28050
SpainSite Not Available
Clinica Universidad de Navarra, Unidad Central de Ensayos Clinicos
Pamplona, 31008
SpainSite Not Available
University Hospital Basel, Department for Medical Oncology
Basel, 4031
SwitzerlandSite Not Available
Kantonsspital St. Gallen, Clinic for Medical Oncology & Hematology
Saint Gallen, 9007
SwitzerlandSite Not Available
University Hospital Zurich, Department of Dermatology
Zurich, 9091
SwitzerlandSite Not Available
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