visugromab (CTL-002)
Biologicalmonoclonal antibody
NCT Number: NCT04725474
The Phase 1 part (Part A) is a dose escalation study of IV visugromab (CTL-002, a monoclonal antibody neutralizing GDF-15) as monotherapy and in combination with an approved checkpoint inhibitor (CPI) in patients with advanced solid tumors.
Enrolment into the Ph 1 part is completed.
The Phase 2 parts (Part B) are cohort expansions with visugromab (CTL-002) in combination with a defined CPI at a fixed dose into seven different solid tumor indications.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Universitätsklinikum Essen, Westdeutsches Tumorzentrum, Innere Klinik und Poliklinik, Essen, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
monoclonal antibody
Time frame: min. 2 months
Incidence of treatment emergent adverse events in monotherapy and/or combination therapy
Time frame: 28 days
Assessment of toxicities in monotherapy and/or combination therapy per dose level
Time frame: min. 6 weeks
RECIST is measured every 6-8 weeks treatment
Time frame: 1 day
PK parameter from serum CTL-002 levels
Time frame: 14 days
PK parameter from serum CTL-002 levels
Time frame: min. 6 weeks
PK parameter from serum CTL-002 levels
Time frame: min. 6 weeks
Measurement of concentration in peripheral blood
Time frame: min. 6 weeks
RECIST is measured every 6-8 weeks during treatment
Time frame: min. 6 weeks
Assessment of appetite via quality of life questionnaire
Time frame: min. 6 weeks
Calculation of BMI in kg/m2 by combining measurement of body weight in kg and body height in cm
Time frame: min. 6 weeks
Combining measurement of L3 vertebra skeletal muscle mass via computed tomography (CT) in cm2 and patient height (squared) in m2
CatalYm GmbH
Industry
A Phase 1/2, FIH, Two-part, Open-label Clinical Trial of Intravenous (IV) Administration of CTL-002 Given as Monotherapy and/or in Combination With an Anti-PD-1 Checkpoint Inhibitor in Subjects With Advanced-stage, Relapsed/Refractory Solid Tumors (The "GDFATHER"-Trial: GDF-15 Antibody-mediaTed Human Effector Cell Relocation).
Acronym: GDFATHER
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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