First-in-Human Study of the GDF-15 Neutralizing Antibody Visugromab (CTL-002) in Patients With Advanced Cancer (GDFATHER)

Last updated: August 7, 2024
Sponsor: CatalYm GmbH
Overall Status: Active - Not Recruiting

Phase

1/2

Condition

N/A

Treatment

visugromab (CTL-002)

Clinical Study ID

NCT04725474
CTL-002-001
  • Ages > 18
  • All Genders

Study Summary

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.

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

Total Participants: 274
Treatment Group(s): 1
Primary Treatment: visugromab (CTL-002)
Phase: 1/2
Study Start date:
December 09, 2020
Estimated Completion Date:
October 31, 2027

Connect with a study center

  • Universitätsklinikum Essen, Westdeutsches Tumorzentrum, Innere Klinik und Poliklinik

    Essen, 45147
    Germany

    Site Not Available

  • Universitätsklinikum Frankfurt, Medizinische Klinik I

    Frankfurt am Main, 60590
    Germany

    Site Not Available

  • Universitätsklinikum Würzburg, Comprehensive Cancer Center

    Würzburg, 97078
    Germany

    Site Not Available

  • Hospital Universitari Vall d'Hebron, Institute of Oncology

    Barcelona, 08035
    Spain

    Site Not Available

  • ICMDiM, Hospital Clinic

    Barcelona, 08036
    Spain

    Site Not Available

  • ICO Hospitalet, Hospital Duran i Reynals

    Barcelona, 08908
    Spain

    Site Not Available

  • Next Oncology, Phase I Unit. IOB - Hospital Quironsalud

    Barcelona, 08023
    Spain

    Site Not Available

  • Hospital Universitario 12 de Octubre

    Madrid, 28041
    Spain

    Site Not Available

  • START Madrid, Hospital Universitario HM Sanchinarro

    Madrid, 28050
    Spain

    Site Not Available

  • Clinica Universidad de Navarra, Unidad Central de Ensayos Clinicos

    Pamplona, 31008
    Spain

    Site Not Available

  • University Hospital Basel, Department for Medical Oncology

    Basel, 4031
    Switzerland

    Site Not Available

  • Kantonsspital St. Gallen, Clinic for Medical Oncology & Hematology

    Saint Gallen, 9007
    Switzerland

    Site Not Available

  • University Hospital Zurich, Department of Dermatology

    Zurich, 9091
    Switzerland

    Site Not Available

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